DNA Analyst Jobs Near Me

BASIC FUNCTION: Omya Technology Center at Cincinnati (OTCC) is looking for a talented, hardworking, inquisitive minded and resourceful Associate Scientist with unique knowledge in the areas of analytical techniques for inorganic and organic materials, glass microsphere production and characterization, glass and ceramic science, test validation and qualification (both with internal and external customers), and data mining. In addition, to ensure that technical service, sales and manufacturing teams receive accurate and timely laboratory support needed to increase sales and/or overcome manufacturing challenges. Provide laboratory leadership for technicians and associate scientists. RESPONSIBILITIES: Interact with other company functions to assist in determining the greatest technical and marketing needs of the organization. Bring ideas to innovation using lean innovation processes to create, select, and commercialize those ideas as fast as possible. Lead and direct laboratory projects, utilizing design of experiments and the scientific method, to address these needs (e.g. customer technical issues or production challenges). Write quality reports detailing the problem, procedure, results and conclusions; educate other laboratory employees by sharing and discussing these projects/reports with them. Provide training, as needed, to less experienced personnel. Perform analyses as needed to expedite testing. Conduct research on perlite, zeolite, and other minerals or products containing silica to increase knowledge of the product and its associated technologies for LWF. Excellent communication, multitasking, and organization skills. Demonstrated hands on research skills. Show expertise with several analytical methods and industry specific processing methods. Assist in the maintenance, calibration and troubleshooting of laboratory equipment. Develop and modify methods and equipment in a safe manner, as needed, to address relevant technical issues. Assist technicians, as needed, to complete testing/experiments in a timely fashion. Familiarity with literature and patent search using multiple tools. QUALIFICATIONS: Bachelor's degree in chemistry, material science, chemical engineering, or another related field. Master's Degree or MBA is a plus. Minimum of 1 - 5 years' technical experience. Experience with application testing. Expertise on light weight fillers materials and applications is a plus. An innovative and flexible mindset with high regard to safety is a must. Understand mathematical and statistical techniques relevant to product testing. Develop a solid understanding of products and applications to provide direction to the team and support project work. Work in an ISO-certified environment. Must possess current US employment authorization. Sponsorship not available for this position. EOE

Primer exists to make the world a safer place. We do this by providing trusted decision-ready AI to the world's most critical organizations. Our software enables leaders, operators, and analysts to better understand the changing world around us in real time and make informed decisions when the stakes are high. Primer has offices in San Francisco, Pasadena, CA, and Arlington, VA. For more information, please visit primer.ai. As a Staff Machine Learning Research Scientist, you will work on some of the deepest problems in machine learning. You will publish papers, attend conferences, and file patents. But you will also ship code right into the products used every day. We call it applied research, and you will be one of the leaders, taking part in a thriving team of engineers whose backgrounds span computer science to particle physics. You will be constantly learning and mentoring, keeping Primer at the leading edge of the most important technology today. Roles and Responsibilities - How You Will Make an Impact Track and understand the machine learning research landscape Help us make the strategic technology investments that ensure Primer's leadership in the space Design, lead, and review experimental work Collaborate and influence cross-functional teams to drive our technology roadmap Lead and mentor data scientists to help them grow Improve and promote best practices across the company and motivate others to follow your high standard Relevant Skills and Experience Graduate degree in computer science or related field 5+ years in machine learning with a focus on machine learning research Demonstrated track record of publications and/or open source projects Hands-on experience with machine learning and NLP tools and libraries from Numpy to PyTorch Curiosity, enthusiasm, and a love for teaching and learning Compensation and Employment Conditions The annual cash compensation range for this position is US$180,000 to US$250,000. Final compensation will be determined based on experience and skills and may vary from the range listed above. This role will consider applicants out of San Francisco, CA or Washington, DC. Primer works closely with the U.S. defense and intelligence establishment. Any offer of employment is conditioned on an applicant or employee being able to meet any applicable government contract requirements. What We Offer We are a series D funded company with investors from Addition, USIT, Lux Capital, Amplify Partners, Addition Capital, Bloomberg Beta, and others. We are intentional about building a diverse and inclusive team of subject matter experts to better advocate for the needs of our users. We care a lot about our work and the well-being of our team. We encourage everyone to work at a sustainable pace and have a flexible vacation policy for team members to utilize, Wellness Days, and 100% paid leave for parents of growing families. We offer competitive compensation and comprehensive benefits. This includes full medical, dental, and vision coverage, fertility benefits through Carrot, mental health coverage on demand with Headspace Care+, Gympass+ Membership via Wellhub, One Medical Membership, 401(k), remote work stipends, and monthly internet allowance. Primer is proud to be an Equal Employment Opportunity and Affirmative Action employer. We do not discriminate based upon race, religion, color, national origin, gender (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, gender expression, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics. If you need assistance or accommodation due to a disability, you may contact us at ***************. Pursuant to the San Francisco Fair Chance Ordinance, we will consider for employment qualified applicants with arrest and conviction records. Apply for this job * indicates a required field First Name * Last Name * Email * Phone * Resume/CV * LinkedIn Profile Website Are you legally authorized to work in the United States? * Select... Will you now or in future require sponsorship for employment visa status (e.g., H-1B, F-1, or TN visa status)? * Select... Do you have a U.S. Security Clearance? * #J-18808-Ljbffr

Kelly Science has and Immediate opening for a Scientist III, QC Labs for our growing client near Columbus, OH Shift: 2nd Full-time Direct Hire Salary: $75,000-$100,000 DOE Your Role: As a Scientist III, QC Labs, you will play a pivotal role in ensuring the highest standards of quality and regulatory compliance. You'll be responsible for conducting sophisticated testing of raw materials, active pharmaceutical ingredients (APIs), and finished products to ensure they meet both customer requirements and regulatory standards. You'll also contribute to the continuous improvement of analytical methods and troubleshooting, working closely with a collaborative team in a fast-paced and ever-evolving environment. Key Responsibilities: Perform Analytical Testing: Conduct qualitative and quantitative chemical and physical testing for APIs, starting materials, packaging components, and finished products, ensuring accuracy and regulatory compliance. Ensure Regulatory Compliance: Maintain adherence to current DPs, SOPs, and cGMP regulations while performing testing and documenting results. Documentation & Reporting: Maintain clear, organized records in laboratory notebooks, worksheets, and documents. Author detailed technical reports to improve analytical methods. Investigative & Troubleshooting Work: Apply advanced analytical techniques to resolve complex issues, investigate discrepancies, and ensure proper use of laboratory equipment. Collaborate with Cross-Functional Teams: Act as a key player in meetings with stakeholders to discuss laboratory deviations, lead troubleshooting efforts, and provide guidance to junior scientists. Review & Approve Analytical Data: Ensure all analytical documentation and batch records are reviewed, validated, and released in accordance with company procedures and specifications. Desired Analytical Expertise: For APIs: Proficiency in UV, HPLC, GC, UPLC, KF, FTIR, Advanced Data Review, Lead Investigator, and Disposition (Packaging/Labeling). For Pharmaceutical Products: Expertise in HPLC, UPLC, Chromatographic Data Systems (Empower preferred), Laboratory Information Management Systems (LabWare preferred), and Advanced Data Review. Additional Desired Techniques: Experience with particle size analysis, ICP, AA, viscosity, XRD, GC, IC, droplet size distribution, FTIR, and microscopy. What You Bring to the Team: A BS in Chemistry (or related science field) with a minimum of 5 years of GMP pharmaceutical analytical chemistry experience, or 10 years of relevant experience with a high school diploma. Hands-on experience executing and evaluating analytical methods for APIs and pharmaceutical products, including both compendial and non-compendial testing. Expertise in advanced analytical techniques, method troubleshooting, and data review. Strong ability to work independently and as part of a team to manage multiple projects simultaneously in a fast-paced environment. Exceptional written and verbal communication skills, including the ability to organize and lead meetings with stakeholders to discuss lab deviations. A collaborative mindset with the ability to mentor junior scientists in laboratory techniques and best practices. What We Offer: Competitive Compensation: Annual performance bonus, commission, and share potential. Comprehensive Benefits: Health, dental, vision, mental health, disability, life insurance, prescription drug coverage, and a variety of voluntary benefits. Generous Time Off: Starting with 20 days PTO (prorated), additional days at milestone anniversaries, 3 personal days, and 11 company-paid holidays. Retirement & Savings: Auto-enrollment in a Hikma-sponsored 401(k) with a 100% match on the first 6% of eligible pay you contribute. Wellbeing & Employee Discounts: Access to our Wellbeing Rewards Program and employee discount offerings. Career Growth: Career advancement opportunities and access to tuition reimbursement to further your education. Family Support: Paid maternity and parental leave to support you during important life milestones. Why Join Us? We value your expertise and dedication. Here, your contributions matter. Join a company that prioritizes safety, quality, and growth. Together, we will innovate, improve, and make a lasting difference in the pharmaceutical industry. Ready to take your career to the next level? Apply now!

This role is part of an evolving hiring need, and openings may become available at different times throughout the year. The timing and number of positions may fluctuate based on business priorities. We encourage interested candidates to apply, and we will reach out as opportunities arise that align with their skills and experience. Our Associate Scientist/Engineer are constantly learning, growing and, ultimately, improving how our products perform. In this role, you will find new ways to innovate, develop and manufacture consumer products. Since we're a highly collaborative company, you will have the opportunity to work with some of the most promising technical and commercial partners, while also mentoring others to realize their fullest potential. We strive to match your skills, qualifications, and interests with a role that works best for you and have a number of areas in Research and Development (R&D) R&D where you could work, including: + Products Research: Deeply understands our consumers and their needs in order to advise product design parameters for new or improved products. + Packaging & Device Development: Builds and improves packages and devices that delight consumers and retailers. Packaging and Devine technologists own the development of packages of superior function and premium design. In addition to ensuring the product functions well once the consumer has brought it home, we place a premium in ensuring that our packages and devices are responsibly developed with sustainability in mind. + Process Development & Pilot Plant Operations: Translates ideas, concepts, and technologies into the design and scale-up of commercially feasible, innovative, chemical and mechanical manufacturing processes. + Modeling and Simulation (M&S): M&S development is a powerful capability which increasingly underpins the work across all our R&D functions. Our M&S experts are developing new to the world mathematical models which speed the pace and impact of our innovations. + Data Science: Communicates sophisticated data or algorithms into simple conclusions that will empower others to drive action based on the insights you derive. As a Data Scientist, you will transform the business to enable better decision-making through the use of sophisticated analytics. Job Qualifications Associate Scientist/Engineer: We believe you will be an excellent fit if you: + Have a BS or MS in engineering, life or physical science field such as Chemistry, Biology, Biochemistry, Analytical and Measurement Science, Microbiology, Packaging Science, or a related field. With a GPA of 3.0 or above on a 4.0 scale. We offer a wide range of roles for Chemical, Mechanical and Biomedical Engineering. Increasingly, we have roles suited for Data Science/Analytics, Electrical and Environmental Engineering or other related engineering fields. + Have critical thinking, active listening, and strong written and verbal communication skills + Positions are located in Cincinnati What we offer: + Responsibilities as of Day 1 - you will feel the ownership of your project from the beginning, and you will be given specific projects and responsibilities. + Continuous mentorship - you will work with passionate people and receive both formal training as well as day-to-day mentoring from your manager. + A dynamic and encouraging environment - working over a diverse array of interesting problems. + Agility and work/life balance for employees, we value every individual and support initiatives. + True support for work/life effectiveness and your long-term well-being. + A competitive salary and benefits' package. Just So You Know: Compensation for roles at P&G varies depending on a wide array of non-discriminatory factors including but not limited to the specific office location, role, degree/credentials, relevant skills, and level of relevant experience. At P&G compensation decisions are dependent on the facts and circumstances of each case. Total Rewards at P&G include salary + bonus (if applicable) + benefits. Your recruiter may be able to share more about our total rewards offerings and the specific salary range for the relevant location(s) during the hiring process. We are committed to providing equal opportunities in employment. We value diversity and do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status. Immigration Sponsorship is not available for this role. For more information regarding who is eligible for hire at P&G along with other work authorization FAQ's, please click HERE (******************************************************* . Procter & Gamble participates in e-verify as required by law. Qualified individuals will not be disadvantaged based on being unemployed. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. Job Schedule Full time Job Number R000124054 Job Segmentation Recent Grads/Entry Level - Campus (Job Segmentation) Starting Pay / Salary Range $85,000.00 - $115,000.00 / year

Forensic Scientist-AG (250002U6) Organization: Attorney GeneralAgency Contact Name and Information: Tina.Webb@ohio AGO.gov Unposting Date: Apr 18, 2025, 3:59:00 AMPrimary Location: United States of America-OHIO-Summit CountyOther Locations: United States of America-OHIO-Franklin County-Columbus Compensation: $30.56/hr - $49.15/hr Schedule: Full-time Work Hours: Monday - Friday 8 - 5Classified Indicator: ClassifiedUnion: Attorney General FOP Primary Job Skill: ForensicsTechnical Skills: ForensicsProfessional Skills: Active Learning, Attention to Detail, Building Trust, Collaboration, Decision Making Agency OverviewAbout Us: The Ohio Attorney General's Office has played a vital role in shaping Ohio's past and present and the work it does today helps chart the state's future. The office consists of nearly 30 distinct sections that advocate for consumers and victims of crime, assist the criminal justice community, provide legal counsel for state offices and agencies, and enforce certain state laws. In these and other capacities, staff members interact with tens of thousands of Ohioans each year. Job DescriptionWhat You'll Do: The Ohio Attorney General's Office is currently seeking a public minded individual for a Forensic Scientist vacancy in the Bureau of Criminal Investigation (BCI) Section within the DNA unit of the Richfield Laboratory. This position will report to the lab every day. The Bureau of Criminal Investigation, known as BCI, is the state's official crime lab serving the criminal justice community and protecting Ohio families. BCI also provides expert criminal investigative services to local, state, and federal law enforcement agencies upon request. With offices throughout the state, BCI stands ready to respond 24/7 to local law enforcement agencies; needs at no cost to the requesting agency. Staff at BCI work every day to provide the highest level of service. This includes special agents who are on call 24/7 to offer investigative assistance at crime scenes, knowledgeable scientists and forensic specialists using cutting-edge technology to process evidence to bring criminals to justice, and criminal intelligence analysts and identification specialists who help local law enforcement solve cases. Experienced special agents, forensic scientists, and other law enforcement experts' staff BCI's three main divisions: 1) Identifications 2) Investigations and 3) Laboratory. The duties for this position include, but are not limited to the following: Under administrative supervision, conducts tests on criminal evidence for DNA analysis (i.e., blood, semen and other body fluids & tissues). Collects, assists or advises in collection and preparation of evidence. Uses and interprets results from appropriate lab instrumentation. Makes conclusions and formulates opinions based on examinations performed. Prepares accurate reports for use by law enforcement officials and courts. Confers with law enforcement officials (e.g., police, deputies, investigators, courts) regarding examinations performed and conclusions reached. Testifies in court concerning evidence examined and analyses performed. Formulates and implements training activities. Advises other employees and law enforcement agencies on topics of analysis, court testimony, interpretation of results and reports, etc. Assists or directs investigators with evidence collection. Gives lectures to community groups. Keeps current with improved or new methods: researches and interprets literature on analytical methods. Develops new methods and maintains professional liaisons with colleagues in DNA testing and research. Performs related miscellaneous lab duties. Performs photographic tasks. Maintains equipment and work area. Prepares reagents and other processing chemicals. Any other related duties as assigned. QualificationsBachelor's degree or an advanced degree in a chemical, physical, biology, or forensic science is required. The bachelor's degree and course content must meet the academic requirements of the laboratory's accrediting body. Coursework in Genetics, Biochemistry, Molecular Biology, Statistics/Population Genetics is required. For courses without these exact titles, the course syllabus or a letter from an instructor may be required. NOTE: A TRANSCRIPT MUST BE INCLUDED WHEN APPLYING FOR THIS POSITION. Job Skills: Forensics, Active Learning, Attention to Detail, Building Trust, Collaboration, Decision MakingSupplemental InformationThe Attorney General's Office is a dynamic organization that offers career opportunities across many different disciplines to people from all backgrounds and experiences. We do not discriminate in any way. All people are equal under the law, and it is so at the AGO. This is a workplace where talent gains you entry and performance determines your career path. Staff can join and lead employee resource groups and participate in online or in-person events to learn about the experiences of others. Employees of the Attorney General's Office must have been in their current positions for at least 12 months in order to be eligible for consideration. The Attorney General's Office may fill additional, similar positions as a result of this posting. The Ohio Attorney General's Office is an Equal Opportunity Employer. AGO# 25-04-065 Background Check Information Selected candidate(s) will be subject to the following background checks: Criminal History Driving Record Taxes Drug Test Polygraph Test Field Investigation In addition, an internet search may be conducted of publicly available and job-related information through social media (Facebook, LinkedIn, Twitter, etc.) or through the use of search engines (Google, Bing, etc.). Employees of the Attorney General's Office must have been in their current positions for at least 12 months in order to be eligible for consideration.ADA StatementOhio is a Disability Inclusion State and strives to be a model employer of individuals with disabilities. The State of Ohio is committed to providing access and inclusion and reasonable accommodation in its services, activities, programs and employment opportunities in accordance with the Americans with Disabilities Act (ADA) and other applicable laws.

Remote work is possible for this position. A Forensic DNA Analyst Level Ill functions in a lead capacity assuming additional responsibilities therein He/she conducts complex analysis on forensic samples and relationships submitted for DNA identification at an advanced level in accordance to established protocol. He/she produces detailed accurate reports of results and conclusions. A Forensic DNA Analyst Level Ill has the ability to operate as a Technical Leader in the absence of the Technical Leader. A Forensic DNA Analyst Level Ill follows all laboratory policies and practices in accordance with federal standards. He/she reports to the Laboratory Director and receives direction from the MUFSC Technical Leader. Knowledge, Skills, and Abilities: Advanced knowledge of laboratory operations including laboratory policies, procedures and objectives. Ability to interpret forensic DNA mixtures, generate statistics and forensic reports Ability to read, analyze and interpret professional journals, technical procedures or governmental regulations Ability to maintain detailed, accurate records and communicate effectively in writing Ability to effectively present complex information and respond to questions from groups of students, customers, and the general public Ability to establish rapport and communicate effectively with law enforcement agencies, faculty, staff, service personnel and students Ability to effectively operate complex computer software utilized in conjunction with laboratory operations Ability to define problems, collect data, establish facts, interpret findings and draw valid conclusions Ability to independently perform a variety of advanced assignments Ability to conduct administrative and technical review of forensic case files Ability to provide expert testimony Physical Demands Agility and coordination in handling equipment and samples as required by laboratory protocol High level of visual acuity Travel may be required Characteristic Duties Works without the benefit of immediate technical supervision. Provides expert testimony Provides general supervision and technical assistance to laboratory technicians and Forensic/ DNA Analyst Levels I and 11 Conducts orientation and training of Forensic DNA Analyst - Trainee Guides and assists Forensic DNA Analyst - Trainee Provides expertise and training in methodology, use of laboratory equipment, quality control/quality assurance, safety, etc. Plans, develops and implements specialized laboratory techniques and analytical procedure Conducts complex forensic DNA analysis and mixture data interpretation/generation of associated statistics at an advanced performance level in accordance to established procedures and protocols Conducts Administrative/Technical Review of forensic DNA Analysis Consults with the forensic community at large on technical issues Troubleshoots for situations involving procedures and equipment Performs validation of new laboratory procedures and equipment Organizes and maintains detailed records, follows established protocols relating to all aspects of laboratory operation. Maintains cleanliness, safety, security and organization of all laboratories and work areas Follows protocols for chain of custody and sample control Prepares reagents and solutions following standardized formulas and protocols Reviews current safety procedures and practices safe storage and handling of hazardous and toxic materials Attends required meetings and participates on committees as directed Participates in the continuing education program. Performs related work as required. Distinguishing Characteristics Functions in a lead capacity, assuming additional responsibilities therein.

About Forge Forge, a member of Ajinomoto Bio-Pharma Services, is a gene therapy development engine, focused on enabling access to life changing gene therapies and helping bring them from idea into reality. We partner with innovators in the gene therapy community: scientists, physicians, biotech/pharma companies, and patient groups. We bring expertise in gene therapy manufacturing and therapeutics development to the table, helping to champion teams that are navigating the long road from the lab bench to the bedside. Our goal is simple but vital to patients living with disease, and we take it seriously. With a patient-first approach, we are forging new models for working together to better accelerate these transformative medicines to reach those who need them the most. About The Team Manufacturing Science and Technology is a team of highly skilled Scientist responsible for the technology transfer of processes developed by Process Development into the GMP Manufacturing area. They are responsible for technical and scientific support for existing clients and internal production. The Manufacturing Science and Technology team develops and implements robust technology transfer, provides data analytics for existing processes and supports continuous improvement of cGMP Manufacturing. Manufacturing Science and Technology interacts with clients through the generation of reports, risk assessments and face to face meetings. About The Role We are currently seeking a Associate Scientist II, Manufacturing, Science & Technology (MS&T) to join the Forge Biologics Team. This is an exciting opportunity to support the MS&T strategy for a Cell & Gene Therapy Contract Development and Manufacturing Organization (CDMO). This includes supporting the development, implementation, and maintenance of all MS&T activities for cell & gene therapy products. As a Associate Scientist II in MS&T, you will be responsible for the successful transfer of viral vector processes into GMP production. What You'll Do (Responsibilities) * Assist Technology transfers from Product Development to Manufacturing. Working with MS&T Scientists defining critical quality attributes, process parameters and conditions of critical importance to manufacturing under cGMPs. * Collaborate closely with cross-functional teams, including clients, Client Development, Technical Sales, Process Development, Manufacturing, Quality, and Program Management, to ensure GMP readiness and provide technical expertise throughout the process * Assist with client-facing functional Lead for Process Technology Transfers by performing detailed review of clients and Process Development process and generates technology transfer documents * Support to General Manufacturing Practices (GMP) execution of the new processes and any deviation investigations, Corrective Action Prevention Plans (CAPAs), and necessary change controls * Provide support for GMP execution, deviation investigations, CAPAs, and change controls * Perform process monitoring (manufacturing data analysis, summary, and presentation), assist with campaign summary reports. * Provides Product Development and Manufacturing with opportunities for process optimization and efficiency enhancements platform manufacturing process. * Recommends improvements for MS&T practices and procedures * Ensure all MS&T activities are in compliance with applicable regulatory requirements, including FDA, cGMP, and international regulatory requirements * Support the development of related documents such as process development plans, manufacturing batch records, and SOPs * Tracks progress of routine manufacturing and tech transfer projects against schedule, provides routine updates and proactively identifies operational risks and remediation. * Investigate new technologies and techniques to reduce costs, improve timelines, enhance safety, and improve regulatory compliance. What You'll Bring (Qualifications) * Master's degree in biology, molecular biology, virology, biochemistry or related discipline, or Bachelor's degree with 2+ years' relevant experience * Proven track record in supporting MS&T teams * Knowledge of FDA, cGMP, and international regulatory requirements * Excellent communication, organizational, and interpersonal skills * Strong problem-solving, decision-making, and leadership skills Work Environment and Physical Demands This position works in both a laboratory environment and typical office environment where the physical work demands will vary depending on the specific tasks and duties required of the job. The employee will be stationary (standing/sitting) for extended periods of time. Employees regularly wear personal protective equipment based on the task being performed. Must be able to work in a confined space, such as a clean room or laboratory environment. Ability to identify small details within the field of vision, distinguish between different colors, and accurately identify objects within a specific area. This job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee. Duties, responsibilities and activities may change or new ones may be assigned. Forge Biologics is an equal opportunity employer dedicated to building an inclusive and diverse workforce. Forge Biologics, provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. Life at Forge We are a team of diverse, driven and passionate people working together to trailblaze a new model for how we make medicines to treat patients with genetic diseases. Our team members use their creativity and talent to invent new solutions, meet new demands, and offer the most effective services in the industry. Forge's core values lay the foundation for H.O.P.E. It provides us a common purpose that we all understand, work towards and live by. HARDWORKING - We work hard and smart, making a persistent and determined effort toward success. Working hard, with focus and desire is the key. OPEN - We strive to be approachable, actively listen and encourage others to contribute and speak up. We positively offer and receive constructive feedback. PURPOSE DRIVEN - We are passionate about working towards and delivering on our mission to manufacture gene therapies. ENGAGED - We are fully absorbed by and enthusiastic about our work and take positive action to further Forge's vision, mission and goals. We've Got You Covered We take the health and happiness of our employees seriously and are consistently evaluating new ways to make our benefits truly UnFORGEttable. * Health, Dental, and Vision insurance that starts on your first day at Forge, with 90% of premiums covered for team members as well as dependents * Flexible PTO (plus 14 paid company holidays) * Annual bonus for all full-time employees * 401(K) company match * Fully-stocked kitchen with free food/drinks * 12 weeks of paid parental leave - additional discount programs include childcare support & dependent care * Employee Assistance Program * Wellness benefits (financial planning services, mental health counseling, employer paid disability) * Professional & Personal development resources - LinkedIn Learning, a dedicate training staff in-house, mentoring opportunities & access to leadership development coaches

ABOUT US Synthesize Bio is an early stage startup using generative AI to fundamentally change life sciences research and accelerate the pace of biomedical discovery. Genomic data are at the heart of most modern molecular studies and tools, from basic research to clinical decision support, but these data are hard to work with. Genomic data require expensive laboratories, sophisticated computational infrastructure, and big teams to produce and analyze. Generating and analyzing genomic data takes weeks or months. We're building generative AI models to cut that time down to minutes or hours. Our platform addresses a huge need in the large and rapidly growing use of genomics in research, from basic science to therapeutic development. mRNA therapeutics alone - a subset of the overall market we serve - is projected to be a $100 billion market by 2026. This is an opportunity to be part of a mission to transform life sciences R&D by dramatically accelerating the pace of discovery. WHO WE ARE Our team has dedicated their careers to moving the needle in biomedical research and education and has a deep understanding of how to build a transformative product in this space. Our founders each have ~20 years of experience in life sciences, genomic data generation and analysis, and AI/ML and data science. Our team has leading experts in the design, execution, collection, and application of AI/ML methods to large biological studies; has previously led and scaled startups; and are experts in scientific training and enablement. We have lived the problem and are ready to solve it! WHAT YOU'LL DO IN THIS ROLE We are looking for a senior computational biologist to join our mission and be an early part of building our AI-powered platform at the intersection of machine learning and life sciences discovery. This role sits on the data team, whose expertise is computational biology. The data team drives the company's internal research, external partnerships, and training data creation. You will help to build out our data and bioinformatics strategy and long-term technical vision. Specifically: Develop internal research leveraging our AI models that showcase their capabilities Develop and execute benchmarking strategies and methods to compare externally developed models to our internal models Enable and support collaborations with potential customers to help them maximize the impact of our platform Provide technical leadership to design and execute data projects TYPICAL QUALIFICATIONS The best candidates do not always match the criteria mentioned in the job description. If you are excited about our vision, meet the minimum requirements, and feel that you could be a valuable asset to our team, please apply. This role requires experience with analyzing genomic sequencing data; the exact types of data and analyses can vary, but a desire and ability to learn quickly is essential. An interest in applying your skills to our mission is the key ingredient. Technical skills & expertise Must have… Demonstrated experience generating insights through analysis of gene expression and other omics data and communicating those results with broad audiences Fluency with data manipulation and processing in R and/or Python (e.g., dplyr and pandas) and collaborating with git/GitHub Excitement about generative AI and interest in employing AI to change how science happens Been part of an informatics, data science, or computational group at a commercial biotech company Ideally you have… Experience managing and working with large datasets in the cloud (AWS, GCP) Familiarity with containers (Docker, Singularity) and workflow managers (Nextflow, WDL, CWL, etc.) Experience and perspective that empathizes with and represents the voices of biomedical research and development customers Experience collaborating with software developers on life science domain-specific applications Experience mentoring junior scientists in best practices and problem-solving including performing code reviews 5+ years post-academic training Approach Open-minded and adaptable; willing to change focus and direction quickly in response to product/market demands Comfortable working both independently and in close collaboration with your own team as well as other teams with complementary expertise Strong communication and desire to be a key player Big-picture thinking while still being hands-on when needed This role is an individual contributor role involving technical project management, but not direct people management. WHY YOU'LL LOVE WORKING WITH US Our founders have strong reputations as thoughtful, forward-thinking colleagues and mentors who cultivate talent. We'll think intentionally and collaboratively about your career and how we build our team. Our founders' experiences in workforce development and commitment to diversity, equity, and inclusion are central to our approach. Impact - Our platform will accelerate the pace of scientific discovery and therapy development to advance human health. This is an opportunity to build something from the ground up in a space that has a real, positive impact. Early employee impact - As a member of the very early team, you will play a pivotal role in helping shape our product, team, and culture. For the rest of our days, no matter how many thousands of people join after you, you will always have that honor and distinction. It looks great on a resume, too. Early stage equity - A benefit of joining early. None of us (neither our founders nor our investors) would be here if we didn't think that our company will create tremendous value over time. Flexible location and hours - We are whole people with whole lives and expect that you are, too. We'll trust each other to make progress as a team, in times and places that work for everyone. Preference for Seattle area. Travel to Seattle will be required from time to time - it's a beautiful city! Visa support - We cannot provide visa support at this time. SALARY Senior Computational Biologist $140-170K Principal Computational Biologist $165-190K

The University of Wyoming is delighted to receive your interest in our vacant position! We strive to connect with qualified and uniquely talented individuals to join our campus community. We would love to hear how your experiences translate to this position, the University's Mission, Vision, and Values, and encourage you to submit an application today! JOB TITLE: Research Scientist, Asst - Veterinary Science Biosafety and Biocontainment Manager JOB PURPOSE: The position serves as Biosafety/Biocontainment Manager within the Department of Veterinary Sciences and Wyoming State Veterinary Laboratory (WSVL), working with the UW Biosafety Officer, UWBF Scientific Director, WSVL Director, and Departmental Head in developing, implementing and managing a comprehensive Biosafety program, including training, record keeping, and operations in support of the UW Biocontainment Facility (UWBF). This position is critical to the safe and effective operation of the UW Biocontainment Facility, which serves as a resource for research and diagnostics on some of the most significant infectious diseases affecting animal and humans in this region. Operations of the UWBF are highly regulated by the Centers for Disease Control and the Animal and Plant Health Inspection Services-USDA under the Federal Select Agent Program (FSAP). ESSENTIAL DUTIES AND RESPONSIBILITIES: Primary duties are to the biosafety program and Select Agent Program that include maintaining detailed records of Select Agent related activities, laboratory-based physical inventory of select agent material, transfer of select agents and performing duties in relation to the FSAP Bio-suitability program. Ability to obtain FSAP Tier 1 approval within one year of employment start date. Ability to enter the UWBF following entry and exit SOP including showering out, and perform physical duties related to maintain safe and efficient operation of the facility. Develop and monitor Standard Operating Procedures (SOPs) to maintain the facility's biological containment, annual facility shutdown/maintenance, training, and building security. Produce and provide biosafety and biosecurity related safety training (including drills and exercises) Perform facility reviews and inspections Advising management and staff on biosafety and biosecurity matters. Serves as primary point of contact and liaison with maintenance and service providers to maintain critical building systems and equipment essential for safe operations, including security systems. Monitor and operate autoclaves, effluent decontamination system, and carcass disposal system. SUPPLEMENTAL FUNCTIONS: Depending on candidate background and interest there may be opportunities to participate in ongoing research-related to operations within the UWBF. COMPETENCIES: Attention to Detail Integrity Safety Awareness: Knowledgeable in matters concerning biosafety and biosecurity at BSL2 and BSL3 levels, including regulatory requirements and facilities Collaboration: Able to work with varied groups including investigators and oversight agencies. Analysis/Problem Identification Technical/Professional Knowledge: Able to operate and train others in the operation of biosafety-related equipment and procedures to include use of respiratory protection, autoclaves, vaporized-hydrogen peroxide and chlorine dioxide systems, and gas incinerators. REMOTE WORK ELIGIBILITY: This position provides vital support to campus customers and requires the successful candidate be available to work on campus. MINIMUM QUALIFICATIONS: Bachelors of Science degree in Biology or closely related field Master's degree obtained before start date At least 2 years of experience working in a BSL3 laboratory DESIRED QUALIFICATIONS: Candidates that are registered biocontainment professionals or have practical research experience at BSL3 or higher levels of containment are preferred Experience working with large and/or small animals Experience supervising a staff member Current or previous security risk assessment and federal select agent program approval are a plus. REQUIRED MATERIALS: Complete the online application and upload the following for a complete application: cover letter, resume or C.V. and contact information for four work-related references. This position will remain open until filled. Complete applications received by 3/4/2025 will receive full consideration. HIRING STATEMENT: UW is an Affirmative Action/Equal Opportunity Educator and Employer (UW Reg 4-1). The University does not discriminate in employment or personnel practices on the basis of race, gender, religion, color, national origin, disability, age, protected veteran status, sexual orientation, gender identity, genetic information, creed, ancestry, political belief, pregnancy, or any other protected category or participation in any protected activity. In compliance with the ADA Amendments Act (ADAAA), if you have a disability and would like to request an accommodation to apply for a position, please call ************ or email **************** ABOUT LARAMIE: The University of Wyoming is located in Laramie, a town of 30,000 in the heart of the Rocky Mountain West. The state of Wyoming continues to invest in its university, helping to make it a leader in academics, research and outreach. The university has state-of-the-art facilities in many areas and the community provides the advantages of a major university. Located in a high mountain valley near the Colorado border, Laramie offers both outstanding recreational opportunities and close proximity to Colorado's Front Range, a bustling group of metropolitan cities including Denver, Boulder, and Fort Collins. This beautiful mountain landscape offers outdoor enjoyment in all seasons, with over 300 days of sunshine annually. For more information about the region, please visit ************************

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries. JOB DESCRIPTION: About Abbott Abbott is a global healthcare leader, creating breakthrough science to improve people's health. We're always looking towards the future, anticipating changes in medical science and technology. Working at Abbott At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You'll also have access to: Career development with an international company where you can grow the career you dream of. Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year. An excellent retirement savings plan with a high employer contribution. Tuition reimbursement, the Freedom 2 Save student debt program, and FreeU education benefit - an affordable and convenient path to getting a bachelor's degree. A company recognized as a great place to work in dozens of countries worldwide and named one of the most admired companies in the world by Fortune. A company that is recognized as one of the best big companies to work for as well as the best place to work for diversity, working mothers, female executives, and scientists. The Opportunity Our nutrition business develops science-based nutrition products for people of all ages, from helping babies and children grow, to keeping adult bodies strong and active. Millions of people around the world count on our leading brands - including Similac , PediaSure , Pedialyte , Ensure , and Glucerna - to help get the nutrients they need to live their healthiest life. Our Nutrition R&D Division is currently hiring for an Associate Scientist I in our Physical Stability Lab. This position works onsite at our Columbus, OH location. This opportunity is for an entry level or early career scientist with interest in macronutrient and mineral testing in food/food products. You are responsible for physical stability testing of infant, adult, and medical nutritional products, assuring quality standards are met. The primary functions of this position are performance of analytical testing on ingredients and finished product as prescribed in various procedures under the guidance of a lab supervisor or test method expert. This position requires producing the highest quality results while operating within the constraints of safety and laboratory policies. Potential opportunity to assist with method development, investigations, and validation projects. What You'll Do Perform routine physical property testing on research and commercial nutritional samples (liquid and powder) to assess product quality during shelf life. Work with multiple experimental methods and various instrumentation to assess physical stability properties of products, ingredients, etc. Maintain good laboratory practices. Perform accurate and precise testing according to laboratory methods. Responsible for keeping up to date with sample due dates and sample backlogs. Operate various types of analytical instrumentation, including maintenance and troubleshooting. Conduct investigations into method deviations and atypical results. Ensure compliance, overall data integrity, and adherence to SOP's, safety, and in-house regulations. Education and Experience B.S. in STEM or related field required OR equivalent experience Proficient in Microsoft Office suite Experience with Sample Manager (LIMS), LabX, or other lab data systems Experience with rheology, particle size, food science, dairy science, protein chemistry, emulsions, and design of experiments (DOE) is an advantage. Ability to work well with others by sharing laboratory equipment and space. Ability to work well in teams by collaborating on projects. Ability to work independently with minimal supervision. Maintain a clean, safe, and orderly work environment. Excellent verbal and written communication skills. Strong drive for results. Understanding of good laboratory documentation practices Ability to troubleshoot and resolve problems, particularly out-of-specification results. Apply Now Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives: ********************** Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity. Connect with us at *************** on Facebook at *********************** and on Twitter @AbbottNews and @AbbottGlobal. The base pay for this position is $46,000.00 - $92,000.00 In specific locations, the pay range may vary from the range posted. JOB FAMILY:Research and Discovery DIVISION:ANRD Nutrition Research & Development LOCATION:United States > Columbus : RP04 ADDITIONAL LOCATIONS: WORK SHIFT:Standard TRAVEL:Yes, 5 % of the Time MEDICAL SURVEILLANCE:No SIGNIFICANT WORK ACTIVITIES:Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day), Continuous standing for prolonged periods (more than 2 consecutive hours in an 8 hour day), Keyboard use (greater or equal to 50% of the workday), Lift, carry, push or pull weights of more than 20 pounds/9 kilos on a regular/daily basis Abbott is an Equal Opportunity Employer of Minorities/Women/Individuals with Disabilities/Protected Veterans.EEO is the Law link - English: ************************************************************ EEO is the Law link - Espanol: ************************************************************

Employment Type: Contract Business Unit: Pre-Pivotal DP Synthetic Enabling Technology Duration: 1+ year Rate: $20-22/Hr 3 Key Consulting is hiring an Associate Scientist for a consulting engagement with our direct client, a leading global biopharmaceutical company. Job Title: Project Manager - REMOTE - (JP9268) Location: Thousand Oaks, CA. (100% REMOTE) Employment Type: Contract Business Unit: Medical Device Supply and Raw Materials Duration: 1+ years (with likely extensions) Notes: Posting Date: 10/14/2021 3 Key Consulting is hiring a Project Manager for a consulting engagement with our direct client, a leading global biopharmaceutical company. Job Description: In this laboratory-based on-site position, you will work within a cutting-edge solid-state chemistry team to support drug development. You will perform several functions and work across Process Development sites as you use solid state characterization tools to derive knowledge that will help drive efficient development and scalable understanding of processes and products in client's small molecule pipeline. The ideal candidate would possess: Proficiency in solid state characterization techniques, such powder X-ray diffraction, particle analysis by laser diffraction, thermal analysis (TGA/DSC), optical microscopy, surface area measurement. Attention to detail, adaptability to new techniques and multiple tasks, ability to solve problem and meet deadlines, and effectiveness to work independently and as a team member. Strong computer skills in instrumentation and data processing in a client-server environment. Excellent communication (verbal and written) and organizational skills. Why is the Position Open? Planned project. Top Must-Have Skill Sets: Experience with solid state characterization techniques. 1-2 years experience Strong knowledge in physical and organic chemistry. Bachelors degree in chemistry or chemical engineering Good verbal and written communication skills Day to Day Responsibilities: Perform solid state characterization measurements and analyses. Design and conduct experiments for form screening and form characterization analysis by following instructions and guidance from project representatives. Interpret data, maintain timely documentation (i.e. electronic notebooks), and contribute to technical reports and presentations in a cross-functional team environment. Participate in lab housekeeping, maintain lab equipment and supplies, and comply with lab safety guidelines. May work occasionally on flexible schedule, i.e. starting early morning or finishing late evening, depending on the project need Basic Qualifications: B.S. with degree in Chemistry, Chemical Engineering, Materials Science, Pharmaceutical Science or related scientific background experience. Pharmaceutical/biotech industry experience preferred, but not required. Demonstrated knowledge of various solid-state characterization techniques such as XRPD, TGA, DSC, particle size, microscopy, surface area, DVS, etc. Good written and oral communication skills. Employee Value Proposition: Candidate would be interfacing with many function areas. Candidate would have a great connection to the pharm development. This is a great hands-on experience and position. Red Flags: No background in physical science No hands on experience with web chemistry labs Interview process: Phone screening followed by in-person interview. We invite qualified candidates to send your resume to **************************. If you decide that you're not interested in pursuing this particular position, please feel free to take a look at the other positions on our website ******************************* You are also welcome to share this opportunity with anyone you think might be interested in applying for this role. hts reserved. Regards, 3KC Talent Acquisition Team

Are you passionate about significantly improving the future of medicine? Do you believe that people are the most important asset of any company? If so, join AmplifyBio! AmplifyBio is a leading contract research organization with a comprehensive range of services that span from being an outsourcing partner for discovery stage R&D work, a preclinical CRO performing safety efficacy and toxicology studies for small molecules and advanced therapies alike, and, most recently, an expansion into manufacturing services for cell, gene, and mRNA-based therapeutics. The AmplifyBio ecosystem is comprised of three distinct business units: ADOC (South San Francisco, CA)- Amplify's Discovery, Optimization, and Characterization laboratories: ASET (West Jefferson, OH) - Amplify's Safety, Efficacy, and Toxicology Site; and the most recently opened AMEC (New Albany, OH) - Amplify's Manufacturing Enablement Center. About ASET West Jefferson, OH: AmplifyBio's safety, efficacy, and toxicology unit (ASET) was launched as a preclinical CRO that spun out of Battelle in 2021 to address the changing needs of commercial organizations developing modern therapeutics. AmplifyBio brings decades of experience to accommodate a wide variety of GLP and non-GLP studies in all in vivo models and dose routes. Among the investments that AmplifyBio has made to empower preclinical assessments of advanced therapies is building a new state-of-the-art analytical laboratory to include molecular and immunological assays that assess critical safety and efficacy indicators for cell and gene therapies during preclinical studies AmplifyBio is currently seeking to hire an Assistant/Associate Scientist to join our growing Analytical Sciences team ! The Assistant/Associate Scientist is responsible for performing analytical testing using a variety of cellular and/or molecular biology analysis platforms. Level of position and title will be based on experience and will report to a supervisor or senior scientist of Analytical Sciences . What You'll Do Here: Perform work in a laboratory setting using a variety of cellular and/or molecular biology analysis platforms. Collect and review data using manual and/or electronic systems. Develop and maintain a good working knowledge of laboratory equipment and experimental procedures to perform assigned laboratory tasks. Communicates routine updates (including technical challenges) on assigned tasks. Recognizes deviations and unusual occurrences notifying responsible individuals promptly and contributes to corrective actions. Complete and maintain training to remain compliant with all regulatory and health/safety requirements. Train less experienced staff as needed. Assists other departments as needed. We Would Love to Hear from You If: Bachelor's degree in molecular biology, Biochemistry, Immunology, Molecular Genetics, or related field. A minimum of 1 year of related work experience in performing cell or molecular assay techniques (e.g., qPCR, dPCR, cytokine analysis, ELISA, PBMC isolation, flow cytometry). Excellent documentation, organization, communication (oral and written), multi-tasking and problem-solving skills. Ability to work independently and in a collaborative team environment. Ability to follow all appropriate regulatory requirements to ensure experimental data are accurately recorded and verified. Ability to work in a BSL-2 research laboratory environment which includes periods of bench-work, working in a bio-safety cabinet, and ability to wear respiratory protection. Must be willing to be immunized with licensed and FDA approved vaccines and medications recommended for persons at risk to occupational exposures. Must have the flexible schedule to accommodate non-standard work hours. Must be able to work more than 40 hours a week (including weekend and holidays) when needed to accomplish necessary tasks. Knowledge of Food and Drug Administration's (FDA) Good Laboratory Practice (GLP) Regulations, 21 CFR Part 58 for the conduct of nonclinical laboratory studies. At AmplifyBio, we're committed to growing and empowering an inclusive community within our company and industry. This is why we hire and cultivate diverse teams of the best and brightest from all backgrounds, experiences, and perspectives across our organization. AmplifyBio is an equal opportunity employer, and we value diversity at our company. We don't discriminate on the basis of race, color, citizenship status, national origin, ancestry, gender (including gender expression and gender identity), sexual orientation, age, weight, religion, creed, physical or mental disability, marital status, veteran status, political affiliation, or any other factor protected by federal, state, or local law. Why You Will Love Working Here: We take the health and happiness of our employees seriously and consistently evaluate new ways to Amp up our benefits to provide an amazing place to work. From a wellness program (did we mention we have an onsite gym with state-of-the-art equipment and ping pong table?), to financial planning and legal assistance, we make sure to take care of our own. Health, Dental, and Vision insurance that starts on your first day at AmplifyBio! Competitive Compensation Package We take work-life balance seriously and we back it up with a FLEXIBLE PTO policy! Generous paid parental leave Wellness and Self-Care Programs 401(k) match Tuition Reimbursement EAP/work-life support system A fun work environment where everyone's voice matters! We are just getting started! More benefits on the way! An Opportunity to Change the World!!! When you join our team, you will be a part of groundbreaking work while collaborating with our clients, research scientists, study directors, lab technicians, and specialists across a variety of disciplines. The future for AmplifyBio is as great as the combination of our imaginations and actions, and we hold ourselves accountable for our choices and results. We have a bias for action, excellence, and, especially, the health and safety of our employees.

SandboxAQ is a high-growth company delivering AI solutions that address some of the world's greatest challenges. The company's Large Quantitative Models (LQMs) power advances in life sciences, financial services, navigation, cybersecurity, and other sectors. We are a global team that is tech-focused and includes experts in AI, chemistry, cybersecurity, physics, mathematics, medicine, engineering, and other specialties. The company emerged from Alphabet Inc. as an independent, growth capital-backed company in 2022, funded by leading investors and supported by a braintrust of industry leaders. At SandboxAQ, we've cultivated an environment that encourages creativity, collaboration, and impact. By investing deeply in our people, we're building a thriving, global workforce poised to tackle the world's epic challenges. Join us to advance your career in pursuit of an inspiring mission, in a community of like-minded people who value entrepreneurialism, ownership, and transformative impact. About the Role SandboxAQ's AI Simulation team develops new drugs and materials using a spectrum of AI and physics-based computational solutions. We are seeking an experienced and innovative Senior AI Computational Biologist to amplify our ability to reason causally about biological systems, based on multimodal data from a variety of inputs, including simulation. The successful candidate will have significant expertise in computational biology, including knowledge of cutting-edge machine learning techniques, particularly involving large graph data structures such as knowledge graphs. They will have experience leading small teams in the delivery of innovative solutions to customers. These skills will be leveraged within a seasoned, agile, and multi-disciplinary group, including drug hunters with an excellent track record in drug discovery, computational chemists, physicists, AI experts, and software engineers. What You'll Do Lead projects combining ML/AI solutions, knowledge graphs, bioinformatics, biophysical simulations, and software development to optimize drug discovery and development strategies. You will guide a technical team to innovate in areas including disease biology, bioinformatics, cheminformatics, AI (e.g., ML, NLP, etc.) using your blend of expertise and knowledge in these areas. Apply your experience in both technical leadership and people management to build a successful and inclusive team. Your work will directly impact decision-making in drug discovery and development projects. Partner with researchers from diverse backgrounds to develop novel computational methods to infer causality in disease progression. Provide broad insight and lead drug projects by providing support on studies in multiple scientific areas including target identification and validation, biomarker discovery, patient stratification, clinical trial design, etc. Interpret experimental data from biological studies in immunology, oncology, and neurodegeneration. Analyze omics and phenotyping data from research studies, clinical trials, and real-world databases to identify disease-driving cell types, pathways, and genes Propose drug targets based on the biology insights derived from data and suggest validation experiments About You You're someone who wants to drive your own development. You're looking for a company where you have the opportunity to pursue your interests across functions and geographies. You are inspired by our mission and have a collaborative, rigorous, and entrepreneurial spirit that matches SandboxAQ's global culture. PhD in computational biology or similar field with strong innovation and publication record. 10+ years of relevant professional experience, including pharma/biotech and postdoctoral research. Experience mentoring direct and/or indirect reports. Excellent analytical capability, being able to identify key questions and come up with innovative solutions for complex problems. You have a unique blend of passion for biology, strong bioinformatics experience (omics, pathway, network analysis, etc.), AI, software development, and literacy on experimental biology to be an effective leader of your team. Enjoys the startup work culture with a great collaborative spirit. A strong team player with good communication skills (especially with experimental biologists). Nice to Haves Proven background in physics-based and AI-based molecular simulation. Experience in target identification. Experience in clinical development or real world data. Experience with biomarker discovery and translation. Experience with text mining or competitor information analysis. Solid biology knowledge in Immunology, Neurodegeneration, and Oncology. Excellent publication record. Willingness to travel less than 25% to conferences, offsites, customers, and internal meetings. The US base salary range for this full-time position is expected to be $179k - $251k per year. Our salary ranges are determined by role and level. Within the range, individual pay is determined by factors including job-related skills, experience, and relevant education or training. This role may be eligible for annual discretionary bonuses and equity. SandboxAQ welcomes all. We are committed to creating an inclusive culture where we have zero tolerance for discrimination. We invest in our employees' personal and professional growth. Once you work with us, you can't go back to normalcy because great breakthroughs come from great teams and we are the best in AI and quantum technology. We offer competitive salaries, stock options depending on employment type, generous learning opportunities, medical/dental/vision, family planning/fertility, PTO (summer and winter breaks), financial wellness resources, 401(k) plans, and more. Equal Employment Opportunity: All qualified applicants will receive consideration regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity, or Veteran status. Accommodations: We provide reasonable accommodations for individuals with disabilities in job application procedures for open roles. If you need such an accommodation, please let a member of our Recruiting team know.

Ohio is a Disability Inclusion State and strives to be a model employer of individuals with disabilities. The State of Ohio is committed to providing access and inclusion and reasonable accommodation in its services, activities, programs and employment opportunities in accordance with the Americans with Disabilities Act (ADA) and other applicable laws. What You'll Do: No ag background, no problem! You'll learn all about agriculture from our top-notch experts who dedicate their lives to a cleaner, safer, better Ohio. This position is responsible for: Performs virological, serological, microbiological, and molecular assays, requiring specialized knowledge, training & judgment within the Animal Disease Diagnostic Laboratory (ADDL) (e.g., virus isolation, virus/serum neutralization, electron microscopy, cell culture, ELISA, PCR) Performs testing to support the bull stud industry in Ohio, including virus isolation and virus neutralization testing Performs testing to support the surveillance of Chronic Wasting Disease in Ohio Performs investigations for unusual or unidentified viruses using virus isolation and electron microscopy Regularly maintains cell lines of animal origin, including quality control, and check for permeability for the virus to be isolated Prepares specimens & follows standard operating protocols to perform various diagnostic assays Participates in proficiency tests for national disease surveillance programs (e.g., Viral hemorrhagic Septicemia virus [VHSV], Spring Viraemia of Carp virus [SVCV]) Validates/verifies new assays Writes SOPs and scientific reports Participate in on-call rotation with other lab staff Maintains laboratory record system (e.g. initial sample identification, log in, transfer of ID through test system, & reporting of results) Maintains accurate & complete laboratory records Receives test specimens Logs in & enters sample identification & test requirements into laboratory information management system (LIMS) Participates in the laboratory's biosafety and Quality Management System Enters results on proper forms & produces final reports Assists Veterinary Virologist in development & validation of new test methods, evaluation & interpretation of test results for identification of viruses & other microorganisms Disposes of biological material with appropriate decontamination procedures Appropriates & maintains control & reference materials for each virology assay Orders & maintains adequate inventory of reagents & other laboratory supplies for molecular diagnostics Carries out laboratory safety related activities Participates in outreach activities This position shall be filled in accordance with the provisions of the OCSEA Collective Bargaining Agreement. ODA bargaining unit members have selection rights before non-bargaining unit members. All other applications will only be considered if an internal bargaining unit applicant is not selected for this position. We Support Diversity and Inclusion: ODA values its internal diversity and pledges to cultivate an inclusive and engaging environment for all employees where differences are embraced and celebrated. The agency commits to building a workforce that champions the advancement of DEI principles and initiatives. The values on which these efforts are founded are\: respect, empathy, transparency, equality, and equal access. What's in it for you: At the State of Ohio, we take care of the team that cares for Ohioans. We provide a variety of quality, competitive benefits to eligible full-time and part-time employees. For a list of all the State of Ohio Benefits, visit our Total Rewards website! Our benefits package includes: Medical Coverage Quality, affordable, and competitive medical benefits are offered through the Ohio Med PPO plan. Dental, Vision and Basic Life Insurance Dental, vision and basic life insurance premiums are free after one year of continuous service. Time Away from Work and Work/Life Balance Paid time off, including vacation, personal, and sick leave 11 paid holidays per year Childbirth/Adoption leave Ohio Public Employees Retirement System OPERS is the retirement system for State of Ohio employees. The employee contributes 10% of his/her salary towards his/her retirement. The employer contributes an amount equal to 14% of the employee's salary. Visit the OPERS website for more information. Deferred Compensation The Ohio Deferred Compensation program is a 457(b) voluntary retirement savings plan. Visit the Ohio Deferred Compensation website for more information. Maternity Benefits Expanded maternity health care benefits available to state employees enrolled in the Ohio Med PPO and Ohio Med NN (narrow network) medical plan options. Several prenatal, childbirth, and post-childbirth services are provided at no out-of-pocket cost to employees utilizing network providers. Examples of services now covered by network providers at 100% include: Prenatal care, including physician visits and examinations. Home health care services designated as maternity care (for expectant members on bed rest). Inpatient claims for all types of delivery. Inpatient NICU claims, from birth through discharge. Postpartum care, including office visits for follow-up, and procedures/treatments directly related to maternity. Medications prescribed for both antepartum and postpartum conditions (e.g., morning sickness, postpartum depression). Medical services provided by non-network providers will be processed at the applicable coinsurance, deductible, and out-of-pocket limits. Prescription drugs that are directly related to maternity care are covered with no copay. The State of Ohio has collaborated with the prescription drug third-party administrator (OptumRx) to provide a list of covered medications that can be approved for zero copay via prior authorization from providers. Candidates must meet one of the following: 42 months of laboratory experience related to the job duties listed above Completion of undergraduate core coursework in biological, chemical, natural, or physical science AND 12 months of related laboratory experience Completion of a Master of Science core program in biological, chemical, natural, or physical science. 12 months of experience as a Laboratory Scientist 1 with the State of Ohio (Job Code\: 83291) An equivalent combination of training and experience as defined above will be considered The State of Ohio is a drug-free workplace which prohibits the use of marijuana (recreational marijuana/non-medical cannabis). Please note, this position may be subject to additional restrictions pursuant to the State of Ohio Drug-Free Workplace Policy (HR-39), and as outlined in the posting. Competitive Salary\: $55,578 - $73,445 Annually Agriculture is the heart of it all in Ohio! The Ohio Department of Agriculture protects all Ohioans by safeguarding plants and animals, conserving our natural resources and supporting farmers. ODA is cabinet-level agency reporting to Governor DeWine. Food and agriculture is Ohio's number one industry, contributing $124 billion to the economy and employing one in eight people. Ohio is home to more than 75,000 farms, with agriculture touching every part of the state. Not only does Ohio rank number one in Swiss cheese production, but we are top three in the nation's egg production and fifth in soybean production. Ohio's farmers impact those well beyond state lines, feeding families across the nation. ODA's beautiful campus is located in Reynoldsburg on 158-acres. Not only is parking free, but food trucks frequent the campus for coffee and lunch. You'll find great coworkers here, who are experts in their field and care about the work they do. What We Do: Working for the Ohio Department of Agriculture means strengthening our state with the help of our 19 divisions programs. Our staff ensures the products you consume every day are safe to eat and drink. We protect Ohio's farmland, improve soil health and water quality, all while keeping our plants, crops, and animals free of pests and disease. We are home to the state's top food safety laboratory and serve as the hub for a statewide lab safety system. Our folks protect consumers by ensuring you get what you pay for through weights and measures accuracy standards. ODA oversees Ohio's 94 county and independent fairs, the showcases of our towns and cities, and protects fair goers by inspecting the amusement rides you love to enjoy! As a member of team ODA, you will be working with people of the highest caliber, doing great work, and making a difference for all Ohioans. The Ohio Animal Disease Diagnostic Laboratory provides veterinary diagnostic services to Ohio's veterinarians and livestock producers. Describe the job duties here in plain language. Focus on the most important aspects of the role. If you require an accommodation for the interview process or the position, please notify the assigned recruiter. Unusual Working Conditions: Exposed to biofluids & tissue, sharps, caustic or toxic chemicals, &/or explosives; may work varying hours. The selected candidate for this position will be required to submit to vaccinations or show proof of vaccination upon selection. For Questions Regarding This Posting Please Contact: Paul Hengstenberg ******************************* The final candidate selected for the position will be required to undergo a criminal background check. Criminal convictions do not necessarily preclude an applicant from consideration for a position. An individual assessment of an applicant's prior criminal convictions will be made before excluding an applicant from consideration. The State of Ohio is a drug-free Workplace which prohibits the use of marijuana (recreational marijuana/non-medical cannabis). The recommended candidate for this position may be required to take a drug screen as part of their approval process. A candidate who tests positive for illegal or improperly used controlled drugs will not be hired. At the State of Ohio, we take care of the team that cares for Ohioans. We provide a variety of quality, competitive benefits to eligible full-time and part-time employees*. For a list of all the State of Ohio Benefits, visit our Total Rewards website! Our benefits package includes: Medical Coverage Free Dental, Vision and Basic Life Insurance premiums after completion of eligibility period

This role is for a Laboratory Scientist. In addition to preparing and analyzing toxicology samples, the Laboratory Scientist I is responsible for preparing and running samples on Immunoassay Units, troubleshooting methods and equipment and preparing data for review. Responsibilities Prepare samples for analysis Set up and run analytical instruments including system suitability, calibration, and QC. Monitor performance of analytical instruments Process data, accept and certify results Train and supervise new staff Organize work and equipment across team for best efficiency Perform advanced instrument troubleshooting and repairs Participate in the implementation of new equipment & methods including installation and validation Make calibration, QC and other solutions Maintain compliance documentation Participate in housekeeping and other general tasks Demonstrate and promote Brightview values Observe and promote safety practices Be a team player and maintain a positive attitude towards work Qualifications College degree in chemistry or related science: BS/BA Working knowledge of instrument and LIS software platforms (LabSolutions, SLS, etc.) Working knowledge of analytical instruments (Shimadzu 8040 LCMS, Synermed IR1200, etc) Proven experience in one or more of the following areas: Troubleshooting and repair/maintenance of LCMS equipment. Operation, troubleshooting, and maintenance of robotic sample preparation equipment Clear communication Strong work ethic and attention to detail Ability to work independently and in a team setting Flexibility to adjust to changing schedules and tasks Ability to use micropipetors and other laboratory equipment Comfort with working with human urine and other biological matrices

Why Sarepta? Why Now? The promise of genetic medicine has arrived, and Sarepta is at the forefront. We hold leadership positions in Duchenne muscular dystrophy (DMD) and limb-girdle muscular dystrophies (LGMDs), and we currently have more than 40 programs in various stages of development in gene therapy, RNA and gene editing. In 2023, we launched our fourth therapy and the first ever gene therapy to treat Duchenne. We're looking for people who see unlimited potential in themselves and who are motivated by an unwavering commitment to patients. What Sarepta Offers At Sarepta, we care deeply about all the people in our community and believe in the importance of supporting them in all aspects of their lives. We aspire to maintain a culture that acknowledges people bring their whole selves to work, and we will strive to help everyone in our community integrate their work and personal lives while maintaining productivity. We are committed to offering a range of benefits and work-life resources designed to support people in the following areas: Physical and Emotional Wellness Financial Wellness Support for Caregivers For a full list of our comprehensive benefits, see our website: ******************************* The Importance of the Role Sarepta Therapeutics is seeking a motivated facility-dependent scientist with expertise in ligand-binding and PCR-based assay development, validation, execution, and reporting with a specific emphasis in non-clinical GLP studies and outcomes. The qualified candidate will provide scientific oversight into the development strategies and validation studies in alignment with current regulatory guidance for Bioanalytical Method Validation. This position will lead day-to-day GCP/GLP analysis on non-clinical and clinical samples, ensuring the requirements of approved protocols, methods, and procedures are upheld. This position will prepare relevant sections of testing study/contributing scientist reports and regulatory documents. The position includes integration of data across platforms, study metadata, and study results for presentation in meetings, reports, and regulatory documents. Additional duties include contributing to laboratory compliance and inspection readiness activities and drafting methods, SOPs, protocols, technical reports, and regulatory document preparation. This role may serve as Study Director for Method Validation and Clinical Testing studies or Contributing Scientist for GLP studies. This position will be a key technical point of contact for Research Operations, Clinical Operations, Data Management, Biostatistics, and vendors for data transfer and analysis needs. The Opportunity to Make a Difference · Conduct GCP/GLP non-clinical and clinical study sample analysis, under the direction of project management teams, using a variety of assay formats such as PCR, IP, Western blot, IHC and NGS while ensuring compliance with associated protocols, methods, and procedures. · Work closely with Quality Control and Quality Assurance to ensure compliance with GDP, GCP, GLP, and appropriate regulatory guidelines, including writing and reviewing SOPs, technical reports, and publications, and maintaining compliant laboratory records. · Contribute to laboratory compliance, inspection readiness activities and regulatory agency related written communications as an SME for this function. Laboratory compliance includes but is not limited to being up to date with the required trainings and following the laboratory cleaning and maintenance SOP. · Take a lead role in the development and validation of fit-for-purpose bioanalytical methods for various clinical stage programs. · Coordinate activities and timelines through close collaboration with project management teams, research teams, as well as cross-functional Translational Biology colleagues. This includes maintaining sample testing trackers, summary statistics for reports, and testing metrics. · Train team members on assays, sample processing and reporting workflows. · Organize and track complex information, prioritize accordingly, and quickly adjust to shifting priorities and demanding timelines to support the overall goals of the department. · Work extended hours as needed, including but not limited to weekend and holiday coverage, occasionally on short notice. · Additional responsibilities as assigned. More about You Knowledge of neuromuscular biology, gene, and si RNA therapies especially in the context of rare genetic disease. Experience with molecular biology assay development including, but not limited to, qPCR, RT-PCR, dd PCR, ELISA, and Western Blot. Demonstrated hands-on experience with PK assays for non-clinical and clinical studies under the GxP umbrella Understanding of drug development, non-clinical safety studies, and experimental design within GLP research environment. Proven scientific leadership when working with collaborative, multi-functional teams. Excellent technical writing and communication skills; able to articulate complex scientific concepts to diverse functional groups and external stakeholders. A strong record of demonstrating critical thinking, decision making, and creative problem-solving skills. Experience with project and data management software (MS Project, WorkFront, PowerBI, etc.) is a plus. What Now? We're always looking for solution-oriented, critical thinkers. So, if you're comfortable with ambiguity and candor, relish challenging yourself, and place kindness and integrity at the forefront of how you approach your peers and work, then we encourage you to apply. #LI-Onsite#LI-TG1This position requires work on site at one of Sarepta's facilities in the United States.The targeted salary range for this position is $102,800 - $128,500 per year. Sarepta is making a good faith effort to be transparent and accurate around our hiring ranges. The salary offer is commensurate with Sarepta's compensation philosophy and considers factors including, but not limited to, education, training, experience, external market conditions, criticality of role, and internal equity.Candidates must be authorized to work in the U.S.Sarepta Therapeutics offers a competitive compensation and benefit package.Sarepta Therapeutics is an Equal Opportunity/Affirmative Action employer and participates in e-Verify.

SpringCreek Fertility is Ohio's premier provider of compassionate and patient-focused fertility & reproductive services, delivered through a dedicated, diverse, and expert team of laboratory, clinical, and administrative professionals. We offer state-of-the-art fertility treatments with an intimate, empathic approach to patient care; we help couples and individuals of all walks of life start their families. If you are a motivated, high-energy, experienced Embryologist who shares our core values of patient-centeredness, teamwork, and a strong commitment to learning and professional development, we would like to meet with you. Mid-level up to Senior Embryologists are invited to apply. The embryologist's primary focus is to participate in the daily operation of the ART Laboratory. This position includes 'hands on' involvement in clinical IVF laboratory work as directed by the Laboratory Director. The Embryology position responsibilities will include all embryology procedures, QA documentation, QC reporting, and associated administrative duties. Ideally, the candidate will have hands-on experience with almost all clinical IVF protocols including, but not limited to: Egg retrieval and processing embryo selection for transfer; Semen analysis for IUI, IVF, and ICSI; Maintaining viability of gametes, tissues, and embryos; Evaluation of fertilization and zygote quality, as well as monitoring of embryo development & grading; Preserving gametes for future use (Oocyte vitrification and sperm sample cryopreservation); Perform donor bank oocyte thaws; Micromanipulation for ICSI, assisted hatching, and trophectoderm biopsy Embryologist Qualifications & Skills Bachelor's or Master's degree in Biology, Embryology, or a related field Minimum of 2 years' experience working in a clinical embryology laboratory Strong understanding of reproductive biology, infertility, and assisted reproductive technologies Demonstrated ability to function effectively without direct supervision and still perform all laboratory services in accord with the Laboratory Philosophy and Operating protocols Excellent organizational, problem-solving, and communication skills An evident commitment to continuous professional development Ability to work well in a fast-paced and high-pressure environment Ability to maintain confidentiality and protect sensitive patient and proprietary information Work weekend and holiday rotations. SpringCreek Fertility offers a generous compensation package, including a sign-on bonus, outstanding selection of employee benefits, including medical, dental, and vision, paid time off, and a 401k with a match. The base salary offered is contingent on education, experience, and demonstrated skills. All offers of employment are conditional upon the successful completion of our hiring process, including verification of eligibility and authorization to work in the United States. We are an equal opportunity employer in all aspects of employment. Confidential letters of interest and CVs should be emailed to: ******************.

Work Your Magic with us! Start your next chapter and join MilliporeSigma. Ready to explore, break barriers, and discover more? We know you've got big plans - so do we! Our colleagues across the globe love innovating with science and technology to enrich people's lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us. This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US. Your Role Manufacture or evaluate products according to established protocols, provide technical support to others and perform operations is support of the group and department. Responsibilities and tasks include: * Safely perform operations to meet quality expectations. * Ensure quality throughout the process. * Regular use of phones, computers and office equipment. * Complete the volume of work required to achieve group/departmental goals and meet deadlines. * Participate as needed in quality audits. * In compliance with change control procedures, improve processes through application of scientific knowledge, experience, and principles. * Identify opportunities for process improvement. Who You Are Physical Attributes: * Wears personal protective equipment. * Will lift up to 50 pounds unassisted. * Sits, stands, walks, reaches, stoops, kneels, crouches, and crawls for extended periods of time. Minimum Qualifications: * Bachelor's degree in chemistry, biochemistry, or other life science discipline. Preferred Qualifications: * Safe chemical handling methods. * Proficiency in MS Word, MS Excel, MS PowerPoint, and the ability to learn and operate other specific application software. * Experience with lab equipment. * 1+ years of experience in a lab. * Strong communication skills, oral and written. * Strong mechanical aptitude. * Proven troubleshooting abilities. * Effective interpersonal and communication skills. * Strong organizational and time management skills. * Knowledge of ISO Quality standards. What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We celebrate all dimensions of diversity and believe that it drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress! Apply now and become a part of our diverse team! If you would like to know more about what diversity, equity, and inclusion means to us, please visit ********************************************************

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic, and labelling is accurate. Eurofins is dedicated to delivering testing services that contribute to the health and safety of society and the planet, and to its corporate responsibility to protect the environment and ensure diversity, equity, and inclusion across the entire network of Eurofins companies. Job Description The Metals Prep Analyst prepares and analyzes environmental samples using standard analytical techniques according to scientific and EPA methodology in compliance with Eurofins Quality Assurance programs and SOP's. Metals Prep Analyst responsibilities include, but are not limited to, the following : Demonstrates and promotes the company vision Regular attendance and punctuality Applies GMP/GLP in all areas of responsibility, as appropriate Performs routine lab tasks that provide experience and familiarization with methods, practices, and programs. These include: Preparation of samples using standard techniques Performing chemical analysis using standard techniques Calculating data Recording and reporting data and any unusual test occurrences to the supervisor Performing routine instrument maintenance Responsible for performing job functions in compliance with Eurofins TestAmerica's EHS and QA standards Responsible for general housekeeping in his/her work area Ability to become trained and competent on complex instrumentation including but not limited to gas chromatography, gas chromatography/mass spectrometry, atomic absorption, ICP, and instrument specific data systems. Works under close supervision using routine and standard methods Aliquots and weighs samples Washes glassware Conducts all activities in a safe and efficient manner Qualifications Basic Minimum Qualifications : BS or BA in chemistry or related field 1-2 years of previous laboratory experience Previous production-oriented work helpful (awareness and ability to meet deadlines) Professional working proficiency in English is a requirement, including the ability to read, write and speak in English Authorization to work in the United States indefinitely without restriction or sponsorship The ideal candidate would possess : Ability to use calculator/mathematical formulas and concepts Ability to complete work within time and quality constraints Can work independently following written or verbal instructions Cooperate and coordinate both orally and in writing Able to follow and learn appropriate protocols in one or more of the following disciplines: Organic preparation Metals preparation and analysis Gas Chromatography Gas Chromatography/Mass Spectrometry Radio Chemistry Wet Chemistry High Resolution preparation and analysis Low Resolution preparation and analysis Additional Information Eurofins Environment Testing, Inc. is searching for a Metals Prep Analyst in our Barberton, OH site. laboratory. Position is full-time, Monday-Friday 1st shift, with overtime as needed. Eurofins Environment Testing (USA) provides a compensation range for informational purposes, the actual base salary may vary based upon, but not limited to, relevant experience and skill set, base salary of internal peers, business sector, and geographic location. We support your development! Do you feel you don't match 100% of the requirements? Don't hesitate to apply anyway! Eurofins companies are committed to supporting your career development. We embrace diversity! Eurofins network of companies believe in strength and innovation through diversity, being an Equal Opportunity Employer. We prohibit discrimination against employees or applications based on gender identity and/or expression, race, nationality, age, religion, sexual orientation, disability, and everything else that makes employees of Eurofins companies unique. Sustainability matters to us! We are well on our way to achieving our objective of carbon neutrality by 2025, through a combination of emission reduction and compensation initiatives. We encourage our laboratory leaders to make sustainable changes at their local level, and in addition to their initiatives we also count on our dedicated carbon reduction team to help us to achieve this goal! Find out more in our career page: ***************************** Eurofins USA Environment Testing is a Disabled and Veteran Equal Employment Opportunity employer.