Senior Scientist, Biology Jobs Near Me

The Senior Materials Scientist is responsible for developing new polymer formulations, working closely with internal functions like Technical Service, Sales, Marketing, Product Management and Manufacturing, and external customers. This individual owns the development of all required instructions, such as bill of materials, inspection plans and key manufacturing process parameters, to ensure that product quality and consistency are maintained. ESSENTIAL DUTIES & RESPONSIBILITIES: Leads development of polymer formulations, meeting customer specifications and internal standards. Applies appropriate theories and scientific principles to new product creation for best solutions. Specifies and as required develops tests to ensure solutions meet or exceed customer specifications. As required recommends specifications for raw materials. Audits raw material suppliers as requested to ensure consistent raw material quality. Provides project management to platform development and large scope development programs. Works with Manufacturing to set target process parameters that can affect product performance and quality. Provides assistance and consultation to Technical Service on resolving product performance issues and processing problems. As requested presents technical papers at industry events and conferences to support, for example, new product launches and to promote thought leadership in the industry. Visits customers to present technical findings and introduce new products and their capabilities Provides technical leadership within the business via consultation and meetings. Works safely and promotes safety via raw material reviews and improved lab practices. Required Skills: 4 year technical degree in engineering or chemistry in a polymers or materials field of study. 3 yrs. of related experience in the plastics or polymers industry, working on product or formulation development for polymer applications. Requires working knowledge of polymers and formulation. Ability to develop and expand an understanding and knowledge of products and raw materials. Use of design of experiment techniques and other statistical tests. Individuals in this position must have the ability to actively listen to customers, both internal and external, efficiently identify problem statements and implement solutions in a timely and customer focused manner. Strong analytical skills. Must have the ability to ask probing questions to truly understand product and market opportunities and to apply these customer technical requirements in the development effort. Ability to handle large quantities of projects and to multi-task. Strong project management skills. Must be able to function effectively in a team and matrix environment. Effective oral and written communication skills. Strong computer skills in MS Word, Excel and PowerPoint. Demonstrated success in new product development and launches. Publication of technical papers in industry conferences a plus Granted patents a plus.

Exciting REMOTE leadership opportunity in Botanical and Wetland surveying for one of the top Environmental groups on the west coast. Our client needs a technical expert ready for the next step in their career, a knowledgable Environmental Scientist ready for a promotion or a vetted Environmental leader ready to be part of a winning team. The Ideal candidate would have: 5 years of Environmental experience Pacific Northwest Experience (Washington, Oregon, British Columbia) Wetland Delineation and Plant Identification Experience Proven leader with no need for supervision from higher ups This position offers a fully remote schedule or a choice to be hybrid to one of their locations, a comprehensive benefits package, and a 20% bonus paid out yearly! ersg are an equal opportunities employer; we are committed to promoting equality of opportunity for all job applicants. We do not discriminate against applicants on the basis of age, sex, race, disability, pregnancy, marital status, sexual orientation, gender reassignment or religious background; all decisions are based on merit.

CFD Research is seeking highly qualified candidates for an imaging scientist position. The candidate will have a PhD in Imaging Science or similar discipline. The ideal candidate will have a deep understanding of the image chain and radiometry. Experience working with Hyperspectral Images (HSI) and Multispectral Images (MSI) for the Visible, SWIR, MWIR, and LWIR is required. Responsibilities will include analysis of data from novel sensors using simulation tools (DIRSIG or FLITES), generating data for AI/ML algorithms, and providing domain expertise on imagery for AI/ML testing and process development Basic Qualifications: • PhD in Imaging Science or a related discipline is Required • Proficiency in AI/ML data curation Techniques • Experience with modeling and simulation of radiometric data • Prior experience developing code to process passive sensor data, apply computer vision, or signal processing algorithms • Ability to communicate technical information clearly and effectively • Experience working on a cross-functional team developing solutions to complex tasks • Active curiosity and a desire to learn and grow as a technical expert Candidate must be a U.S. Citizen and possess the ability to obtain and maintain a security clearance. Preferred Qualifications: • Experience with Digital Imaging and Remote Sensing Image Generation(DIRSIG) • Experience with XPATCH • Experience with FLITES • Experience with Scene Generation Location: This role is based in the Dayton, OH area, and is 100% onsite. About CFD Research: Since its inception in 1987, CFD Research has delivered innovative technology solutions within the Aerospace & Defense, Biomedical & Life Sciences, Intelligence & Sensing, and Energy & Materials industries. CFD Research has earned multiple national awards for successful application and commercialization of innovative component/system technology prototypes, multi-physics simulation software, multi-disciplinary analyses, and expert support services. Based in Huntsville, Alabama where laboratory facilities and headquarters are located, CFD Research also has office and laboratory facilities in Dayton, Ohio, prototyping test and evaluation facilities in Hollywood, Alabama, and office facilities in Fort Walton Beach, Florida. CFD Research is an ISO9001:AS9100D registered company and is appraised at CMMI Level II for Services. CFD Research is a 100% ESOP (employee-owned company) recognized in Inc. Magazine's Inc5000 as a top growing company for four of the last five years. Learn more at ******************** Benefits: CFD Research offers competitive salaries and excellent employee benefits, including an employer matching 401(k) and Employee Stock Ownership Plan (ESOP). CFD Research offers a highly competitive insurance package, including medical, vision, and dental insurance. We offer company paid leave, compensation time, parental leave, long-term and short-term disability, accidental death and dismemberment, and life insurance. Performance appraisals occur twice a year and annual pay increases are based upon corporate goals, personal development, performance, and outstanding achievements. In addition, group and individual bonuses are awarded for exceptional performance. CFD Research is an EO employer - Veterans/Disabled and other protected categories

We are looking for an *advanced chemist* to join our team to train AI models. You will measure the progress of these AI chatbots, evaluate their logic, and solve problems to improve the quality of each model. In this role you will need to hold an expert understanding of chemistry- a completed or in progress Masters/PhD is preferred but not required. Other related fields include, but are not limited to: Formulation Scientist, Development Chemist, Analytical Chemist, Chemical Engineer, Medicinal Chemist, Biochemist, Process Development Chemist. Benefits: * This is a full-time or part-time REMOTE position * You'll be able to choose which projects you want to work on * You can work on your own schedule * Projects are paid hourly starting at $40+ USD per hour, with bonuses on high-quality and high-volume work Responsibilities: * Give AI chatbots diverse and complex chemistry problems and evaluate their outputs * Evaluate the quality produced by AI models for correctness and performance Qualifications: * A current, in progress, or completed Masters and/or PhD is preferred but not required * Fluency in English (native or bilingual level) * Detail-oriented * Proficient in chemistry and inductive/deductive reasoning, physical/temporal/ spatial reasoning Note: Payment is made via PayPal. We will never ask for any money from you. PayPal will handle any currency conversions from USD. #INDUSCHM Job Types: Full-time, Part-time Pay: From $40.00 per hour Benefits: * Flexible schedule Location: * Cleveland, OH (Preferred) Work Location: Remote

Staff Machine Learning Research Scientist 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 Location This role will consider applicants out of San Francisco, CA, or Washington, DC. Compensation The annual cash compensation range for this position is US$225,000 to US$250,000. Final compensation will be determined based on experience and skills and may vary from the range listed above. Government Compliance 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. The company may rescind any offer of employment to an applicant or terminate an employee if the applicant or employee is unable to perform the functions of the position in compliance with applicable government contracts or if an applicant or employee makes a false attestation of compliance. 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 about 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. #J-18808-Ljbffr

Leonardo.Ai seeks a Senior Research Scientist to join our expanding global AI team. We're advancing our generative AI platform to empower millions, regardless of expertise, with intuitive tools for creating high-quality images and videos. Now part of Canva, we're ready to build a world-class R&D team to seamlessly integrate AI products, tools, and features, making creativity limitless for nearly a quarter of a billion users. The Role: As a Senior Researcher, you will play a pivotal role in building and training new foundational models as we advance further into image, video, 3D, and language modelling. We are working at the cutting edge of what's possible and pushing every day to go beyond it. Responsibilities: Lead Multimodal Research: Spearhead research in multimodal AI, including image, video, 3D, and language modelling. Drive cross-modal innovation to address complex challenges across media types. Foundational Model Development: Architect, train, and evaluate foundational models. Research and Application: Work in exploratory phases to gain new insights and apply them to improving model outcomes. Skills we love you to have: Multimodal AI Expertise: Experience in text-to-image, video comprehension and synthesis, 3D generation, with knowledge of training LLMs for multimodal applications. Foundational Model Building and GPU Proficiency: Skill in building foundational models from scratch, leveraging GPU technology for performance and scaling. Advanced Model Architectures: Background in GANs, transformers, and diffusion models, especially for multimodal applications, keeping up with industry advancements. Academic and Open-Source Contributions: Record of peer-reviewed publications and contributions to open-source projects. Technical Proficiency: Expertise in Python, frameworks such as PyTorch or Jax, and cloud computing. Collaborative Attitude: Strong team player experienced in cross-functional collaboration. Competitive Edge: Stay ahead of industry trends with AI-based literature, competitors, and emerging technologies. Help maintain our competitive edge in the market by providing insights and recommendations. Educational Background: PhD or Master's in AI or similar field with proven research experience. Our Culture: Inclusive Culture: We celebrate diversity and are committed to creating an inclusive environment where everyone feels valued and empowered. Flexible Work Environment: We understand the importance of work-life balance. Enjoy the flexibility to work remotely or from our vibrant offices. Empowering Growth: Your development is our priority. We offer continuous learning opportunities and career growth tailored to your goals. Impactful Work: Join us in shaping the future of AI. You'll work on innovative projects that have a meaningful impact. Next Steps: If you're passionate about AI research and have a history of implementing AI models, this role might be the perfect fit for you. We encourage you to apply and start the conversation whether you're based locally in the USA or overseas. Why Leonardo.Ai? Shape the Future of AI: Join us in revolutionising content creation and build a platform at the forefront of generative AI. Hybrid and Remote Options: Flexibility is key. Choose a work arrangement that suits your lifestyle. Benefits: We offer a generous package including paid parental leave and a wellness budget. Diversity and Inclusion: We intentionally seek people from a variety of backgrounds to join our team. Typical Interview Process While we love technology, our interview process is all human. A Talent team member will review your application, and we'll contact you either way. Here's what you can expect: Round 1 - Meet Your Recruiter: Our Talent team will arrange a 30-minute video call to discuss your experience and the role. Round 2 - Craft Interview: You'll meet team members to discuss the technical task and your expertise. Round 3 - Technical Task: You may be given a short take-home task to assess your skills. Round 4 - Values Interview: You'll meet with the Department Head for a conversation about your potential impact. Important Information If there are any adjustments we can make to make you more comfortable at any point in the interview process, please let us know. #J-18808-Ljbffr

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

The Organization What's happening at Entrada Therapeutics? Entrada is a clinical-stage biopharmaceutical company aiming to transform the lives of patients by establishing a new class of medicines that engage intracellular targets that have long been considered inaccessible. Our Endosomal Escape Vehicle (EEV)-therapeutics are designed to enable the efficient intracellular delivery of a wide range of therapeutics into a variety of organs and tissues, resulting in an improved therapeutic index. Through this proprietary, versatile and modular approach, Entrada is advancing a robust development portfolio of RNA-, antibody- and enzyme-based programs for the potential treatment of neuromuscular, ocular, metabolic and immunological diseases, among others. Our lead oligonucleotide programs are in development for the potential treatment of people living with Duchenne who are exon 44, 45 and 50 skipping amenable. We have also partnered to develop a clinical-stage program, VX-670, for myotonic dystrophy type 1. We are a tight-knit team of experts and leaders in both therapeutic development and rare diseases and are excited to grow and attract colleagues who are ready to join a high-energy, dedicated team that likes to get things done and dramatically improve the lives of patients and their families. The Perfect Addition to Our Team You are a highly motivated, collaborative, and innovative Drug Metabolism and Pharmacokinetics expert with experience driving preclinical DMPK activities. We have a diverse pipeline and as such you should have experience across both small and large molecules and have hands on experience leading the design, analysis, and interpretation of preclinical in vitro and in vivo studies. You are an exceptional communicator and a natural collaborator who is excited about the opportunity to contribute to this function and work closely with cross functional leaders. The Opportunity The ideal candidate will serve as a subject matter expert working within the DMPK team to drive the DMPK strategy across all designated programs and pipelines. They will have the opportunity to design, manage, and execute DMPK deliverables, and will be responsible for analyzing, interpreting, and authoring/reviewing ADME and PK/PD reports. Responsibilities Lead all PK- and ADME-related efforts for designated program(s). Communicate and present relevant information across all areas of the organization, regardless of level. Select and manage PK/TK, PK/PD, and ADME CROs. Author and review PK/TK, PK/PD, and ADME reports. Author and review relevant PK/TK, PK/PD, and ADME sections of regulatory submission documents (e.g. investigational new drug (IND), investigator brochure (IB), clinical trial application (CTA), etc). Review associated reports, including clinical, toxicology, pharmacology, and bioanalysis. Collaborate with clinical teams, including pharmacology, biomarkers, development, and operations. Collaborate with non-clinical development teams, including toxicology and bioanalysis. Collaborate with discovery teams to guide future programs and better understand mechanisms of action. This is a US based remote position, with preference given to local New England based candidates. This role will require minimum monthly or quarterly travel to the Entrada Therapeutics Headquarters located in Boston, MA. The Necessities At Entrada, our passion for science, our devotion to patients and our values drives our behavior: Humanity - We genuinely care about patients and about one another. Tenacity - We are relentless and persistent in the pursuit of developing therapies for patients. Creativity - We are creative problem solvers. Collaboration - We are more than the sum of our parts. Curiosity - We have a growth mindset and push conventional thought and theory. To thrive on our team, you will need to come with: PhD in pharmacology or similar field with 8+ years of DMPK experience in an industry setting or a MS with 12+ years of relevant experience. Expertise with ADME studies and assays, with a proven track record of strategizing and troubleshooting based upon raw data. Vendor Management experience, specifically managing CROs. Additional experience with other aspects of ADME, bioanalytical techniques, PK/PD, toxicokinetics, pre-clinical PK/PD modeling, and translational biology are strongly preferred. Experience with oligonucleotide-based modalities. Experience authoring and reviewing DMPK-related reports and regulatory documents for health authority submissions is highly desirable. You should be naturally collaborative and a strong communicator, and let's not forget the ability to multi-task effectively and work within aggressive timelines- these are key to being successful in Entrada's fast paced environment. The Perks By becoming a team member here at Entrada, you'll have access to competitive health, dental, and vision coverage, as well as life insurance, and short term and long-term disability insurance. We value work life balance, you'll benefit from discretionary time off, paternity leave, and an excellent 401(k) package. We also offer a generous transportation stipend to commute as you wish. Our location in the vibrant and growing Seaport District is close to all the best that the city of Boston has to offer. Entrada Therapeutics is an equal opportunity employer. Qualified candidates will receive consideration for employment without regard to race, color, religion, national origin, gender, sexual orientation, gender identity or expression, age, mental or physical disability, and genetic information, marital status, citizenship status, military status, protected veteran status or any other category protected by law. #J-18808-Ljbffr

Genesis Research is an international healthcare consultancy providing value evidence strategy, generation, synthesis, and communication services to Life Sciences companies. Delivering these services empowered by technology innovations has enabled us to become a trusted partner with our clients across the development and commercialization life cycle. Combining both traditional and novel analytical approaches with diverse real-world data, including genomic, medical record, claims and patient-reported information, has allowed us to inform Life Science company internal decision making as well as submissions and presentations to regulators; health technology assessment authorities and payers; the medical community; and, patient organizations. We are looking for an experienced Principal Scientist to join our Analytics team. Accountabilities within this role: Develop efficient and error-free code using SAS/R and SQL that accurately applies the methodologies defined to complete the analysis. Produce and present client-ready tables and charts with strong aesthetics ready to present both internally and to clients by utilizing Excel & PowerPoint. Contribute to the development and growth of protocols and statistical analysis plans by providing analytical, database, therapeutic, epidemiological, and statistical expertise and experience. Design, implement and interpret basic & advanced statistical methods. Working knowledge of multiple databases that are commonly utilized. Conceptualize the scope of projects and time required from project initiation through completion of client deliverables. Handle multiple concurrent projects/tasks and meet all internal and external deadlines by effectively managing one's own time. Provide proactive, responsive, high quality execution of client deliverables. Lead proposal development with oversight from client director, lead client meetings, assist with development of scientific communications (abstracts/posters). Qualifications: Bachelor's degree in a technical or quantitative field from an accredited college or university (e.g., statistics/ biostatistics, epidemiology, bioinformatics, health economics, mathematics, outcomes research, public health, biology, medicine); Masters, MPH or PhD degree preferred. 4+ years relevant work experience (less with PhD). Demonstrated knowledge of R/SAS and statistical methods over a 6+ year period. Experience developing and implementing statistical analysis plans utilizing RWD or clinical trials. Demonstrated thorough aptitude for conducting quantitative and qualitative analyses. Willingness to provide superior customer service through first-rate work product. Ability to work independently and collaboratively. Strong communication skills with the ability to explain technical data analysis results to business people, as well as communicate quantitative challenges and issues to technical people. Knowledge Preferred: Significant experience working with analytical models and visualization techniques and tools. Advanced analytics techniques (regression, simulation, etc.). Identifying and addressing client needs, building relationships with clients, developing requests for proposals. Creative and innovative problem solving skills. Ability to work under tight deadlines in a highly dynamic environment. Compensation: Competitive salary Performance-related bonus Hybrid/Remote work environment Private insurance Flexible PTO plan and many company holidays including the last week of the year Genesis Research is an equal opportunity employer. #J-18808-Ljbffr

City/State Norfolk, VA Work Shift First (Days) Sentara Norfolk General Hospital in Norfolk, VA is hiring an experienced Sr. Laboratory Scientist to work full days in Microbiology. Generous Sign on Bonus up to $20,000 for qualified candidates! As a Sr. Laboratory Scientist, duties are to perform laboratory testing and interpret test results using scientific knowledge and principles of test procedures and disease processes; recommends contingency testing. Directly responsible for developing, maintaining, and managing daily technical operations, including staff training and education, implementation of instrumentation, and accreditation readiness. Education Bachelor's in medical technology or Biology/Chemical Science Certification/Licensure ASCP or AMT certification Experience 3 year of experience Microbiology experience Chat with our Laboratory Services recruiters every Wednesday from 1PM-2PM EST. Click this link to be register for the virtual chat: keyword: MLS, medical laboratory scientist, MT, medical laboratory technologist, CLS, Clinical lab Specialist, Talroo-Allied Health , Laboratory Services, #Indeed, #zip . We provide market-competitive compensation packages, inclusive of base pay, incentives, benefits, and equity. The base pay rate for Full Time employment is:$29.21 - $48.68 Benefits: Caring For Your Family and Your Career • Medical, Dental, Vision plans • Adoption, Fertility and Surrogacy Reimbursement up to $10,000 • Paid Time Off and Sick Leave • Paid Parental & Family Caregiver Leave • Emergency Backup Care • Long-Term, Short-Term Disability, and Critical Illness plans • Life Insurance • 401k/403B with Employer Match • Tuition Assistance - $5,250/year and discounted educational opportunities through Guild Education • Student Debt Pay Down - $10,000 • Reimbursement for certifications and free access to complete CEUs and professional development • Pet Insurance • Legal Resources Plan • Colleagues may have the opportunity to earn an annual discretionary bonus if established system and employee eligibility criteria is met Here at Sentara, we are committed to consistently enhancing our training, advancement tracks, work-life benefits, and more. Our goal is to make you feel more excited to be here every day! Sentara Norfolk General Hospital , located in Norfolk, VA, is a 525-bed tertiary care facility that is home to the only Level I Adult Trauma Center and burn trauma unit in Hampton Roads, and also serves as the primary teaching hospital for Eastern Virginia Medical School. In addition to the high-quality heart program at Sentara Heart Hospital, our facility is home to Nightingale Regional Air Ambulance and several other dedicated facilities and specialized services. As a recognized accredited Comprehensive Stroke Center, and Magnet hospital for nursing excellence, our hospital specializes in heart and vascular, neurosciences, neurosurgery, urology, oncology, spine care, advanced imaging, behavioral health, maternity, and women's health, including a state-of-the-art neonatal intensive care unit. Sentara Health is an equal opportunity employer and prides itself on the diversity and inclusiveness of its close to an almost 30,000-member workforce. Diversity, inclusion, and belonging is a guiding principle of the organization to ensure its workforce reflects the communities it serves. In support of our mission “to improve health every day,” this is a tobacco-free environment. For positions that are available as remote work, Sentara Health employs associates in the following states: Alabama, Delaware, Florida, Georgia, Idaho, Indiana, Kansas, Louisiana, Maine, Maryland, Minnesota, Nebraska, Nevada, New Hampshire, North Carolina, North Dakota, Ohio, Oklahoma, Pennsylvania, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Washington, West Virginia, Wisconsin, and Wyoming.

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 and live in the state of NJ. Sponsorship not available for this position and EOE

Our client is seeking a highly motivated Associate Scientist with experience or interest in in vitro diagnostic (IVD) assay development to join our dynamic team. This company has combine biotechnology with healthcare to commit to cancer research and innovative treatments! Located in Cleveland, OH Direct Hire Pay: $55k-75k Essential Duties & Responsibilities Perform assigned laboratory testing under supervision with clear instructions Conduct routine and semi-routine tasks with increasing independence Execute laboratory techniques and experimental procedures according to defined protocols Prepare reagents and solutions required for experiments Carry out tests and procedures in accordance with standard protocols Handle human biological specimens (e.g., blood, plasma, urine, and other bodily fluids) following biosafety guidelines and regulatory requirements Perform routine maintenance and general laboratory upkeep Accumulate, organize, and analyze experimental data Document procedures, observations, and results accurately according to Company and GDP policy Assist in preparing and presenting project data for internal discussions Participate in technical discussions and project meetings Ensure compliance with all safety and company policies Perform all other duties as assigned Qualifications Education & Experience: Bachelor's degree in Biology, Biochemistry, Molecular Biology, Biomedical Engineering, or a related field with 1-4 years of relevant experience Master's degree with 0-1 years of experience Industry experience preferable Technical Skills: Hands-on experience with standard laboratory techniques such as pipetting, reagent preparation, and handling (Experience with automated immunochemistry analyzers preferred) **This job description is a complete list of all desired skills, but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!**

Our client is seeking a highly motivated Scientist with experience or interest in in vitro diagnostic (IVD) assay development to join their growing and dynamic team. This role will require hands-on execution of experiments, routine lab maintenance, and documentation to support product development, validation, and verification initiatives. Responsibilities Perform assigned laboratory testing under supervision with clear instructions Conduct routine and semi-routine tasks with increasing independence Execute laboratory techniques and experimental procedures according to defined protocols Prepare reagents and solutions required for experiments Carry out tests and procedures in accordance with standard protocols Handle human biological specimens (e.g., blood, plasma, urine, and other bodily fluids) following biosafety guidelines and regulatory requirements Perform routine maintenance and general laboratory upkeep Accumulate, organize, and analyze experimental data Document procedures, observations, and results accurately according to Company and GDP policy Assist in preparing and presenting project data for internal discussions Participate in technical discussions and project meetings Ensure compliance with all safety and company policies Perform all other duties as assigned Qualifications Bachelor's degree in Biology, Biochemistry, Molecular Biology, Biomedical Engineering, or a related field with 1-4 years of relevant experience Master's degree with 0-1 years of experience Hands-on experience with standard laboratory techniques such as pipetting, reagent preparation, and handling (Experience with automated immunochemistry analyzers preferred) Ability to follow standard protocols and troubleshoot routine lab tasks Experience with data analysis and documentation best practices Familiarity working in an FDA or ISO-regulated environment is a plus Proficient computer skills especially with Microsoft Office applications

Dr. Mitchel Stacy Lab A postdoctoral research position is immediately available within the Center for Regenerative Medicine at Nationwide Children's Hospital working in the lab of Dr. Mitchel Stacy. Read more about the lab at the link below: Stacy Lab | Nationwide Children's Hospital Research in the lab is focused on the development and validation of quantitative imaging techniques that allow for characterization of cardiovascular diseases and vascular remodeling. Of particular interest is PET imaging of skeletal muscle perfusion and PET-based molecular imaging of vascular biology. The lab utilizes multiple imaging modalities, which include clinical and micro PET/CT, CT angiography, and ultrasound. The lab is equipped with a variety of image processing workstations, which include dedicated software for PET/CT image analysis, ANSYS for computational modeling research, dedicated tools for ultrasound image analysis, and a dedicated angiography workstation. Experimental work and training will be focused on pre-clinical models of vascular disease (small and large animal) and clinical cardiovascular imaging. Clinical imaging projects will be conducted in collaboration with The Ohio State University College of Medicine and additional pediatric hospitals across the United States. Candidates should be highly motivated with an interest in biomedical imaging, vascular biology, and/or skeletal muscle biology. Also required are excellent written and verbal communication skills, as the position will involve participation in manuscript and grant writing. For more information related to the lab's research, please refer to a list of recent publications... ********************************************************************** Keywords PET imaging Biomedical imaging Vascular Biology Cardiovascular Disease Nuclear Medicine Skeletal Muscle Biology Job Duties: Performing pre-clinical and clinical imaging experiments Design and conduct scientific experiments to obtain data Write and publish scientific manuscripts and journals Contribute to grant submissions for external funding Qualifications: Ph.D. or M.D. in Physiology, Biomedical Engineering/Sciences, or related field Desire to pursue a career in biomedical imaging and/or vascular surgery research Appropriate knowledge base and/or skills related to the topic area Good writing and verbal communication skills

Senior/Staff Bioinformatics Production Scientist We are seeking a highly motivated, results-oriented, and collaborative individual to join our Bioinformatics and Analytics team as a Senior/Staff Bioinformatics Production Scientist. In this role, you will combine genomics expertise with strong production engineering skills to design and implement robust, scalable computational pipelines for large-scale NGS data processing and interpretation. This role is critical in advancing our bioinformatics capabilities to ensure best-in-class performance for Twist Bioscience's production pipelines. You will be responsible for architecting high-throughput workflows, maintaining reliable bioinformatics infrastructure, and collaborating with Field Application Scientists (FAS) to optimize pipelines that directly support customer needs and field operations. Key Responsibilities Pipeline Design & Implementation Develop and maintain production-grade bioinformatics pipelines for NGS data processing using modern workflow frameworks (e.g., Nextflow, Airflow). Ensure pipelines are scalable, reproducible, and optimized for high-throughput sequencing data. Integrate best practices in software development, including CI/CD, containerization (Docker, Singularity), and cloud-based execution. Work directly with Field Application Scientists (FAS) to understand their workflow needs and translate them into robust, user-friendly bioinformatics solutions. System Architecture & Production Engineering Lead architectural decisions for bioinformatics workflows in cloud-based or on-prem environments. Collaborate with DevOps teams to maintain monitoring, logging, and alerting systems for pipeline reliability and performance. Design and implement data storage solutions for large-scale genomic datasets, balancing accessibility, cost, and efficiency. Develop standardized deployment methods for field-facing applications and pipeline updates. Collaboration & Cross-Functional Support Partner with FAS teams to troubleshoot pipeline-related issues and improve field operations. Work closely with wet-lab scientists and assay development teams to provide bioinformatics insights for product troubleshooting and optimization. Collaborate with other Senior Bioinformatics Scientists to ensure consistency in data processing pipelines and best practices. Required Qualifications Education & Experience: Master's degree with 6-8 years of industry experience, or a Ph.D. with 3+ years of industry experience in Bioinformatics, Computational Biology, Computer Science, or a related field. Bioinformatics & Production Pipeline Expertise: Experience designing, implementing, and optimizing production-scale bioinformatics pipelines for NGS data. Strong understanding of workflow orchestration frameworks (e.g., Nextflow, Snakemake, Airflow). Hands-on experience with large-scale genomic data processing and storage solutions. Background in assay development, genomics-based diagnostics, or quality control for high-throughput NGS data. Software Development & DevOps Skills: Proficiency in Python. Strong familiarity with containerization (Docker, Kubernetes), CI/CD, and cloud platforms (AWS, GCP, or Azure). Experience with monitoring, logging, and alerting tools for bioinformatics workflows. Cross-Functional Collaboration & Support: Ability to work closely with Field Application Scientists, translating field needs into scalable computational solutions. Strong troubleshooting skills and the ability to identify, debug, and resolve pipeline-related challenges in a high-throughput environment. Preferred Qualifications Experience with Rust, C++, SQL/dbt is a plus Strong grasp of infrastructure automation, cloud-native workflows, and scalable computing architectures. Familiarity with databases (SQL, dbt) and distributed computing frameworks. Experience with high-performance computing (HPC) environments and storage optimization strategies. About Twist Bioscience Twist Bioscience synthesizes genes from scratch, known as “writing” DNA. Just as children learn to both read and write, the next phase of development for the genomics revolution is the ability to write DNA. At Twist Bioscience, we work in service of people who are changing the world for the better. In fields such as health care, agriculture, industrial chemicals and data storage, our unique silicon-based DNA Synthesis Platform provides precision at a scale that is otherwise unavailable to our customers. Twist Bioscience Corporation is an Equal Opportunity Employer. Twist Bioscience Corporation provides equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, genetic characteristics, or any other category protected by law. San Francisco applicants: Pursuant to the San Francisco Fair Chance Ordinance, we will consider for employment qualified applicants with arrest and conviction records.

The Opportunity QuidelOrtho unites the strengths of Quidel Corporation and Ortho Clinical Diagnostics, creating a world-leading in vitro diagnostics company with award-winning expertise in immunoassay and molecular testing, clinical chemistry and transfusion medicine. We are more than 6,000 strong and do business in over 130 countries, providing answers with fast, accurate and consistent testing where and when they are needed most - home to hospital, lab to clinic. Our culture puts our team members first and prioritizes actions that support happiness, inspiration and engagement. We strive to build meaningful connections with each other as we believe that employee happiness and business success are linked. Join us in our mission to transform the power of diagnostics into a healthier future for all. The Role The Production Scientist is familiar and competent to perform all manufacture, qualification testing and manufacturing release testing for all product types within department. The Production Scientist transfers new product development from multiple company sources for their department and area of responsibility. The position is also accountable for the technical training, maintenance, product improvement projects, customer and internal investigations for those products. This role is located in Athens, Ohio. The Responsibilities * Identifies and resolves assay performance issues by developing scientific plans and approaches and designing experiments to develop and optimize assays. Summarizes experimental data and draws conclusions independently. Communicating conclusions, improvements and corrections with Department Management. * Reviews relevant literature and employs creative thinking and application to problem solving. Investigates the feasibility of applying a wide variety of scientific concepts to potential products and implements new methods or procedures. * Plans and executes experiments and validation of protocols while maintaining detailed and organized project documentation in accordance with internal and external regulatory requirements as part of the design control process. Responsible for determination of feasibility, process development, validation, creation and implementation of documentation. * Reads, understands and follows cGMP, QSOPs and SOP documentation. Understands each department's product lines and their production processes and performs job duties in accordance with required documentation while completing procedures and records in a timely and accurately fashion. * Works with minimal supervision and resolves problems independently or collaboratively in a timely manner in order to minimize disruptions in production schedule or product development transfer. Maintains work flow with efficient use of equipment and material resources to maintain production and transfer schedules. Collaborates with other Production Scientist, Department Management and Research Department on the direction and expenditure of employee and equipment resources within departments. * Serves as a resource for Manufacturing Associates and Technicians for issues and training. Ensures that any staff participating in the manufacture or testing of department's product lines are trained and performing the tasks according to the required documentation. * Operates all lab equipment with understanding of proper operation, preventative maintenance and safety considerations of the required equipment. Maintains manufacturing areas in accordance with QSOP and safety documentation. The Individual Required: * Bachelor's or Master's degree in life sciences or equivalent, 4+ years practical experience, and demonstrated working knowledge of research & production methods. * Associates Degree in life sciences or equivalent, 6+ years practical experience, and demonstrated working knowledge of research & production methods. * 10 years practical experience, and demonstrated working knowledge of research and/or production methods * Problem solving and troubleshooting skills * Effective communication skills required including ability to work with multiple people * Computer skills in Microsoft Word, Excel or similar programs * Good laboratory skills including maintaining orderly and safe work areas * This position is not currently eligible for visa sponsorship. Preferred: * Familiarity with cGMPs and FDA guidelines for biological industries preferred. The Key Working Relationships Internal Partners: Interacts with all levels of Operations' employees, participates in cross-functional teams and supports interdepartmental project teams. Trains staff and works with Management on troubleshooting and corrective actions. The Work Environment The work environment characteristics are representative of both an office and laboratory environment. The Physical Demands Handling of viral and bacterial hazards as well as infectious or potentially infectious bodily fluids, tissues and samples. Position requires ability to lift up to 20 lbs. on a regular basis. Walking, standing, and sitting for long periods of time (up to 75% of the day) are routine to accomplish tasks in this role. Specific vision abilities required by this job include close and distance vision and the ability to adjust focus. Personal protective equipment is required as posted. Equal Employment Opportunity QuidelOrtho believes in Equal Opportunity for all and is committed to ensuring all individuals, including individuals with disabilities, have an opportunity to apply for those positions that they are interested in and qualify for without regard to race, religion, color, national origin, citizenship, sex, sexual orientation, gender identity, age, veteran status, disability, genetic information, or any other protected characteristic. QuidelOrtho is also committed to providing reasonable accommodations to qualified individuals so that an individual can perform their duties. If you are interested in applying for an employment opportunity and require special assistance or an accommodation to apply due to a disability, please contact us at **************************. #LI-HF1

The Opportunity QuidelOrtho unites the strengths of Quidel Corporation and Ortho Clinical Diagnostics, creating a world-leading in vitro diagnostics company with award-winning expertise in immunoassay and molecular testing, clinical chemistry and transfusion medicine. We are more than 6,000 strong and do business in over 130 countries, providing answers with fast, accurate and consistent testing where and when they are needed most - home to hospital, lab to clinic. Our culture puts our team members first and prioritizes actions that support happiness, inspiration and engagement. We strive to build meaningful connections with each other as we believe that employee happiness and business success are linked. Join us in our mission to transform the power of diagnostics into a healthier future for all. The Role The Production Scientist is familiar and competent to perform all manufacture, qualification testing and manufacturing release testing for all product types within department. The Production Scientist transfers new product development from multiple company sources for their department and area of responsibility. The position is also accountable for the technical training, maintenance, product improvement projects, customer and internal investigations for those products. This role is located in Athens, Ohio. The Responsibilities Identifies and resolves assay performance issues by developing scientific plans and approaches and designing experiments to develop and optimize assays. Summarizes experimental data and draws conclusions independently. Communicating conclusions, improvements and corrections with Department Management. Reviews relevant literature and employs creative thinking and application to problem solving. Investigates the feasibility of applying a wide variety of scientific concepts to potential products and implements new methods or procedures. Plans and executes experiments and validation of protocols while maintaining detailed and organized project documentation in accordance with internal and external regulatory requirements as part of the design control process. Responsible for determination of feasibility, process development, validation, creation and implementation of documentation. Reads, understands and follows cGMP, QSOPs and SOP documentation. Understands each department's product lines and their production processes and performs job duties in accordance with required documentation while completing procedures and records in a timely and accurately fashion. Works with minimal supervision and resolves problems independently or collaboratively in a timely manner in order to minimize disruptions in production schedule or product development transfer. Maintains work flow with efficient use of equipment and material resources to maintain production and transfer schedules. Collaborates with other Production Scientist, Department Management and Research Department on the direction and expenditure of employee and equipment resources within departments. Serves as a resource for Manufacturing Associates and Technicians for issues and training. Ensures that any staff participating in the manufacture or testing of department's product lines are trained and performing the tasks according to the required documentation. Operates all lab equipment with understanding of proper operation, preventative maintenance and safety considerations of the required equipment. Maintains manufacturing areas in accordance with QSOP and safety documentation. The Individual Required: Bachelor's or Master's degree in life sciences or equivalent, 4+ years practical experience, and demonstrated working knowledge of research & production methods. Associates Degree in life sciences or equivalent, 6+ years practical experience, and demonstrated working knowledge of research & production methods. 10 years practical experience, and demonstrated working knowledge of research and/or production methods Problem solving and troubleshooting skills Effective communication skills required including ability to work with multiple people Computer skills in Microsoft Word, Excel or similar programs Good laboratory skills including maintaining orderly and safe work areas This position is not currently eligible for visa sponsorship. Preferred: Familiarity with cGMPs and FDA guidelines for biological industries preferred. The Key Working Relationships Internal Partners: Interacts with all levels of Operations' employees, participates in cross-functional teams and supports interdepartmental project teams. Trains staff and works with Management on troubleshooting and corrective actions. The Work Environment The work environment characteristics are representative of both an office and laboratory environment. The Physical Demands Handling of viral and bacterial hazards as well as infectious or potentially infectious bodily fluids, tissues and samples. Position requires ability to lift up to 20 lbs. on a regular basis. Walking, standing, and sitting for long periods of time (up to 75% of the day) are routine to accomplish tasks in this role. Specific vision abilities required by this job include close and distance vision and the ability to adjust focus. Personal protective equipment is required as posted. Equal Employment Opportunity QuidelOrtho believes in Equal Opportunity for all and is committed to ensuring all individuals, including individuals with disabilities, have an opportunity to apply for those positions that they are interested in and qualify for without regard to race, religion, color, national origin, citizenship, sex, sexual orientation, gender identity, age, veteran status, disability, genetic information, or any other protected characteristic. QuidelOrtho is also committed to providing reasonable accommodations to qualified individuals so that an individual can perform their duties. If you are interested in applying for an employment opportunity and require special assistance or an accommodation to apply due to a disability, please contact us at **************************. #LI-HF1

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 si RNA therapeutics biomarker assays. 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 clinical testing study 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 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 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. More about You BS degree in scientific discipline/MS or Ph.D. preferred, with 3+ years of laboratory experience in the healthcare, biotech/pharmaceutical industry, or equivalent. Knowledge of neuromuscular biology, gene and si RNA therapies especially in the context of rare genetic disease. Demonstrated hands-on experience with implementation of biomarker analysis in clinical laboratory studies under regulatory guidelines. Laboratory experience in biomarker assay development, transfer, validation under GCP/GLP compliant conditions. Understanding of late-stage drug development, clinical operations and experimental design within clinical 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 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.

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 ********************************************************