Forensic Scientist Jobs Near Me

INEOS Pigments is one of the largest producers of titanium dioxide in North America and the leading producer of titanium chemicals. We operate a state of the art manufacturing complex with leading technology and more than 45 years of manufacturing excellence. We supply a complete range of TiO2 products for the most demanding end use applications. Our global supply chain network coupled with our local sales network will deliver products around the world. We are committed to providing you with the best products, the best service and the best value. If you have a titanium dioxide or titanium chemicals inquiry we will be pleased to hear from you. This position is part of the Technology and Innovation (T&I) division. The role is primarily responsible for providing technical support to our Sales and Marketing department for existing and new products. A key component of the role is developing and maintaining technical relationships at key customers within a defined geography and applying technical knowledge to identify solutions to a diverse range of customer issues. The position also performs varied laboratory assignments to provide technical support to Manufacturing, Sales & Marketing, Supply Chain, and Product Stewardship, and provides applications development support to Product Development. BS in Chemistry, Polymer Chemistry, Polymer Engineering, or allied field. 5 years' experience in plastics or polymers preferred Six Sigma Green Belt or Black Belt certification is highly desirable. Level & Type of Knowledge, Experience & Skills Required: Plastics/Coatings/Paper industry formulating and processing experience Experienced in building good relationships with internal and external partners, preferably within a commercial environment. Proven presentational skills and competent public speaker. Experience in leading technical projects Versatile being able to work in a team, work independently, or take leadership role as necessary to complete task. Ability to travel 30% of the time Business/Industry Specific: Experience working in a commercial manufacturing organization. Knowledge of compounding and plastics processing Hands-on experience with plastics compounding, extrusion, and/or molding processes and equipment

Outlier helps the world's most innovative companies improve their AI models by providing human feedback. Are you an experienced Biology who would like to lend your expertise to train AI models? About the opportunity: Outlier is looking for talented Biology or related fields expert to help train generative artificial intelligence models This freelance opportunity is remote and hours are flexible, so you can work whenever is best for you You may contribute your expertise by…Assessing the factuality and relevance of domain-specific text produced by AI models Crafting and answering questions related to BiologyEvaluating and ranking domain-specific responses generated by AI models Examples of desirable expertise:A bachelor's or higher degree in Biology or a related subject Experience working as an Biology professional Ability to write clearly about concepts related to Biology in fluent EnglishPayment:Currently, pay rates for core project work by Biology experts range from $30 to $50 per hour USD. Rates vary based on expertise, skills assessment, location, project need, and other factors. For example, higher rates may be offered to PhDs. For non-core work, such as during initial project onboarding or project overtime phases, lower rates may apply. Certain projects offer incentive payments. Please review the payment terms for each project.

RELOCATION ASSISTANCE: No relocation assistance available CLEARANCE TYPE: SecretTRAVEL: Yes, 10% of the TimeDescriptionAt Northrop Grumman, our employees have incredible opportunities to work on revolutionary systems that impact people's lives around the world today, and for generations to come. Our pioneering and inventive spirit has enabled us to be at the forefront of many technological advancements in our nation's history - from the first flight across the Atlantic Ocean, to stealth bombers, to landing on the moon. We look for people who have bold new ideas, courage and a pioneering spirit to join forces to invent the future, and have fun along the way. Our culture thrives on intellectual curiosity, cognitive diversity and bringing your whole self to work - and we have an insatiable drive to do what others think is impossible. Our employees are not only part of history, they're making history. Northrop Grumman Cybersecurity has a need for an experienced Cyber Forensic Specialist. This role can be 100% virtual/work from home. We prefer candidates who are located near our Redondo Beach, CA facility. Job Duties: Resolves cyber forensic issues using computer host analysis, network resource, and log analysis techniques. Discovers, analyzes, diagnoses, and reports on user activity, files and network events and vulnerability issues. The role of the analyst is to recover data, such as documents, photos and e-mails from computer hard drives, and other devices and other data storage devices, such as SSD, flash drives, mobile communications devices and legacy technologies, that have been deleted, damaged or otherwise manipulated. The analyst must also provide timely and cogent analysis to the requesting customer and maintain excellent record keeping and evidence storage practices. This analysis is in support of internal investigations conducted by the Northrop Grumman Law Dept, Security, Employee Relations and Ethics, as well as other entities as directed. The incumbent will serve as a subject matter expert on a variety of issues and will routinely interface with external stakeholders, including legal counsel, law enforcement and fellow technical experts, as well as corporate leadership. Develops analysis and make recommendations for the purchase and utilization of hardware and or software that will address specific customer requirements and will maintain proficiency on all forensic platforms employed. Develops policies and procedures to investigate user behavior by means of automated information systems. Assists in the development and delivery of computer forensic security awareness products and briefings. Basic Qualifications: Must have at minimum, a Master's Degree with 3 years of experience OR a Bachelors Degree with 5 years of experience. OR additional years of experience in lieu of a degree. Must have prior experience working in the field of cyber forensics, preferably in either a law enforcement or corporate capacity Must have at least 40-60 hours of formal classroom training in forensic software and techniques. Must have proficiency in mobile forensics using either GrayKey or VeraKey software. This position has the ability to be 100% virtual/work from home. Occasional local travel to Redondo Beach, CA facility will also be required. Candidates must be comfortable with collaborative technologies such as Skype, Microsoft Teams, and/or Zoom Must have/maintain reliable and fast data connection will be the responsibility and expense of the employee Must have a dedicated place to work that is sufficiently secure (proprietary data and company-owned equipment will be in the employee's possession and must be secured). Ability to obtain and maintain a DoD Top Secret Security Clearance Preferred Qualifications: Bachelor's or Master's Degree in Cyber Forensics, Computer Systems Management, Information Security or similar field is desired. Salary Range: $100,300.00 - $150,500.00The above salary range represents a general guideline; however, Northrop Grumman considers a number of factors when determining base salary offers such as the scope and responsibilities of the position and the candidate's experience, education, skills and current market conditions.Employees may be eligible for a discretionary bonus in addition to base pay. Annual bonuses are designed to reward individual contributions as well as allow employees to share in company results. Employees in Vice President or Director positions may be eligible for Long Term Incentives. In addition, Northrop Grumman provides a variety of benefits including health insurance coverage, life and disability insurance, savings plan, Company paid holidays and paid time off (PTO) for vacation and/or personal business.The application period for the job is estimated to be 20 days from the job posting date. However, this timeline may be shortened or extended depending on business needs and the availability of qualified candidates.Northrop Grumman is committed to hiring and retaining a diverse workforce. We are proud to be an Equal Opportunity/Affirmative Action Employer, making decisions without regard to race, color, religion, creed, sex, sexual orientation, gender identity, marital status, national origin, age, veteran status, disability, or any other protected class. For our complete EEO/AA and Pay Transparency statement, please visit *********************************** U.S. Citizenship is required for all positions with a government clearance and certain other restricted positions.

Note: Fully onsite - 9-5 Monday - Friday (may be occasional WFH opportunities) Ideal Candidate: 1 year of hands on experience in a lab environment. M.S. is preferred, B.S. is acceptable. No PHD candidates. Skills: General lab experience, protein knowledge required. Nice to have: UPLC experience, hands on experience with proteins. UF & DF experience Responsibilities will include: Participate in the planning, design, execution, and documentation of studies related to drug product formulation and process development in support of commercialization and life cycle management of biologics. Support and conduct related studies, e.g. UF/DF, filtration, freeze/thaw and fill/finish, for products in various formulations and formats (liquid, lyophilized, etc.). Evaluate process and product performance through analytical testing via measurement of pH, conductivity, osmolality, protein concentration, HPLC and CE methodologies, solid state characterization, particle quantitation/characterization, physical properties, etc. Data analysis and documentation/review in electronic notebooks. Author, review, and data verify technical documents such as protocols, reports, regulatory documents, etc. Clearly and consistently communicate data in progress reports and presentations. Participate in cross-functional teams in a fast-paced environment to progress product development. Adhere to all training, compliance, and safety guidance. Support lab operations and inspections as required of all lab-based staff. Work primarily onsite with remote work as appropriate to role and tasks. Preferred Qualifications: Degree in Engineering, Chemistry, Pharmaceutics, Materials Science, or related discipline. 2+ years of relevant lab experience. Understanding of physical/chemical stability of proteins. Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with procedures and policies. Proficient computer skills. Self-motivation, adaptability and a positive attitude. Critical thinking, problem solving, and independent research skills. Good organizational skills with strong attention to detail. Excellent communication (oral and written). Basic Qualifications Bachelor's Degree Top 3 Must Have Skill Sets: Lab Experience: Hands-on experience in a laboratory setting is crucial. This includes familiarity with lab equipment, techniques, and safety protocols. Work in a Team: The ability to collaborate and work well within a team is essential. This involves effective communication, cooperation, and the ability to contribute to group projects. Communication: This includes drafting technical reports, presenting study objectives and results, and facilitating discussions. Pay Rate between $29 - $33/Hr on W2 based on experience. "This posting is for Contingent Worker, not an FTE"

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.

Battelle delivers when others can't. We conduct research and development, manage national laboratories, design and manufacture products and deliver critical services for our clients-whether they are a multi-national corporation, a small start-up or a government agency. We recognize and appreciate the value and contributions of individuals with diverse backgrounds and experiences and welcome all qualified individuals to apply. Job Summary Battelle is currently seeking a highly skilled and motivated Protein biochemist for the National Security Business Unit. This full-time position is located in Columbus, Ohio. Some domestic and international travel is anticipated. This is an in-person position. As a Protein Biochemist, you will assume a pivotal role in conducting cutting-edge research by leveraging your expertise in molecular biology, protein purification, characterization, and functional analysis. The successful candidate will showcase technical leadership and provide invaluable support in laboratory studies, including the production and characterization of proteins and enzymes. Additionally, you will actively identify and capitalize on opportunities to lead projects that enhance capabilities and foster the development of novel technical approaches. This position offers an exhilarating opportunity to collaborate with a dynamic, multidisciplinary team committed to advancing scientific knowledge and generating significant contributions to the field of protein biochemistry. Responsibilities Conduct DNA isolation, purification, and quantification, as well as PCR amplification and cloning. Design and execute experiments to purify, characterize, and analyze proteins using various biochemical and biophysical techniques. Work independently to meet study objectives and deliverable with some oversight Conduct protein expression, purification, and characterization using a range of methodologies including chromatography, electrophoresis, and mass spectrometry. Perform functional analysis to characterize the biological and biochemical properties of target proteins. Develop and optimize protein purification protocols and methodologies for improved yield and quality. Analyze and interpret experimental data, and contribute to the preparation of technical reports, manuscripts, and presentations. Some domestic and potential international travel is anticipated. Key Qualifications MS and 2 years of experience or BS and 4 years of experience in biochemistry or a related field. Expertise in protein purification techniques such as affinity chromatography, size exclusion chromatography, and ion exchange chromatography using chromatography systems such as AKTA or NGC. Proficiency in protein characterization techniques including SDS-PAGE, Western blotting, and/ or mass spectrometry. Expertise in protein expression systems (e.g., E. coli, yeast, mammalian cells) and recombinant protein production. Excellent problem-solving skills, critical thinking abilities, and attention to detail. Strong communication and interpersonal skills, with the ability to work collaboratively in a team-oriented environment. Ability to travel. Sufficiently medically fit to work in the laboratory and in the field to perform assigned duties. U.S. citizenship, with the ability to obtain and maintain required government security clearances as a condition of employment. Preferred Qualifications Experience working within laboratory quality management systems (e.g., ISO 9001, ISO17025, GLP). Experience with using plasmid editing software. Benefits: Live an Extraordinary Life We care about your well-being, not just on the job. Battelle offers comprehensive and competitive benefits to help you live your best life. Balance life through a compressed work schedule: Most of our team follows a flexible, compressed work schedule that allows for every other Friday off-giving you a dedicated day to accomplish things in your personal life without using vacation time. Enjoy enhanced work flexibility, including a hybrid arrangement: You have options for where and when you work. Our Together with Flexibility model allows you to work 60% in-office and 40% remote, with Monday and Tuesday as common in-office days, dependent on team and position needs. Take time to recharge: You get paid time off to support work-life balance and keep motivated. Prioritize wellness: Stay healthy with medical, dental, and vision coverage with wellness incentives and benefits plus a variety of optional supplemental benefits. Better together: Coverage for partners, gender-affirming care and health support, and family formation support. Build your financial future: Build financial stability with an industry-leading 401(k) retirement savings plan. For most employees, we put in 5 percent whether you contribute or not, and match your contributions on top of that. Advance your education: Tuition assistance is available to pursue higher education. A Work Environment Where You Succeed For brilliant minds in science, technology, engineering and business operations, Battelle is the place to do the greatest good by solving humanity's most pressing challenges and creating a safer, healthier and more secure world. You will have the opportunity to thrive in a culture that inspires you to: Apply your talent to challenging and meaningful projects Receive select funding to pursue ideas in scientific and technological discovery Collaborate with world-class experts in an inclusive environment Nurture and develop the next generation of scientific leaders Give back to and improve our communities Vaccinations & Safety Protocols Battelle may require employees, based on job duties, work location, and/or its clients' requirements to follow certain safety protocols and to be vaccinated against a variety of viruses, bacteria, and diseases as a condition of employment and continued employment and to provide documentation that they are fully vaccinated. If applicable, Battelle will provide reasonable accommodations based on a qualified disability or medical condition through the Americans with Disabilities Act or the Rehabilitation Act or for a sincerely held religious belief under Title VII of the Civil Rights Act of 1964 (and related state laws). Battelle is an equal opportunity employer. We provide employment and opportunities for advancement, compensation, training, and growth according to individual merit, without regard to race, color, religion, sex (including pregnancy), national origin, sexual orientation, gender identity or expression, marital status, age, genetic information, disability, veteran-status veteran or military status, or any other characteristic protected under applicable Federal, state, or local law. Our goal is for each staff member to have the opportunity to grow to the limits of their abilities and to achieve personal and organizational objectives. We will support positive programs for equal treatment of all staff and full utilization of all qualified employees at all levels within Battelle. The above statements are intended to describe the nature and level of work being performed by people assigned to this job. They are not intended to be an exhaustive list of all responsibilities, activities and skills required of staff members. No statement herein is intended to imply any authorities to commit Battelle unless special written permission is granted by Battelle's Legal Department. For more information about our other openings, please visit ************************

CAS uses intuitive technology, unparalleled scientific content, and unmatched human expertise to help companies create groundbreaking innovations that benefit the world. As the scientific information solutions division of the American Chemical Society, CAS manages the largest curated reservoir of scientific knowledge, and for 117 years, has helped innovators mine, assess and apply that information to keep businesses thriving. The CAS team is global, diverse, endlessly curious and strives to make scientific insights accessible to innovators worldwide. CAS is currently seeking a Biochemist on our Content Operations team. This position is located at our headquarters in Columbus, Ohio Position Summary: The Biochemist applies scientific expertise, analytical skills, problem-solving capabilities, and relevant language skills to help build CAS's world-class collection of scientific data. Primary responsibilities include Job Accountabilities: * Leverage scientific and technical knowledge to curate high-quality research data from patent and journal literature in the Life Sciences content area in a production environment. * Provide scientific and content knowledge, capabilities, insights, and solutions for other CAS functions. * Identify and implement process improvements by planning, managing, and participating in unit-level projects, and leveraging data analysis skills. Qualifications: * An advanced degree in Biochemistry or related scientific field. A bachelor's degree with extensive professional experience will be considered. * Education or professional experience with enzymes, agrochemistry, food chemistry, cosmetics, or pharmaceuticals a plus * Excellent scientific reading comprehension and writing skills. * Excellent team player who is organized and willing to adapt to the needs and requirements of an agile organization. * Demonstrates a proactive and flexible attitude, with a keen willingness to show initiative. * Solid analytical and problem-solving skills. * Ability to work independently as well as part of a team. * Ability to learn policies, work habits, insights, and tool usage from trainers to foster quality and productivity. * Effective organizational skills, including attention to detail, time management, and multi-tasking. * Familiarity with video conferencing, instant messaging, email, calendar scheduling, word processing, spreadsheets, and document sharing software. * Japanese, Korean, or other language skills a plus CAS offers a competitive salary and comprehensive benefits package, including a generous vacation plan, medical, dental, vision insurance plans, and employee savings and retirement plans. Candidates for this position must be authorized to work in the United States and not require work authorization sponsorship by our company for this position now or in the future. EEO/Minority/Female/Disabled/Veteran

Requisition ID req32151 Working Title HS/Associate Scientist 1 Grade 12 Position Summary The Prevention Research Center (PRC) at the University of New Mexico is looking for a highly motivated and creative Associate Scientist 1 to work with a multidisciplinary research team in the development, implementation and evaluation of social marketing campaigns for health promotion and disease prevention. Eat Smart to Play Hard (ESPH) is one of those social marketing campaigns funded by the Supplemental Nutrition Assistance Program- Education (SNAP-Ed). ESPH works with children 8 - 11 years old and their families to support them in their healthy lives. The main goal is to make it convenient and fun for the children to eat more fruits and vegetables as a way to get to their goal of playing hard. Other social marketing initiatives developed at the Center are with teens and older adults. The successful candidate will: Collaborate with the social marketing team in the planning, development, and implementation of new and existing social marketing initiatives at the PRC. Design and independently execute the new research and program concepts, protocols, and procedures to reduce obesity and chronic related diseases, applying diversified knowledge of public health, nutrition, social marketing and relevant scientific principles, practices, and methods. Analyze, evaluate, and interpret research data, such as process evaluation and focus groups, and prepare summations for review by investigators and other team members. Contribute to the development of summary reports, presentations, and manuscripts associated with our research findings. Provide professional guidance, leadership, and instruction to new staff and students engaged in social marketing efforts. Work closely with parent champions and volunteers in the communities implementing our programs like Eat Smart to Play Hard (ESPH) and I Choose H2O. Ensure proper care in the use and maintenance of equipment and supplies; promote continuous improvement of workplace safety and environmental practices. Ensure purchasing for program maintenance, operation, and troubleshooting of the program's equipment, materials, and promotion. See the Position Description for additional information. Conditions of Employment For individual positions in which driving is a job requirement, a valid NM driver's license and valid UNM driver's permit will be required. Successful candidate must submit to post-offer, pre-employment physical examination and medical history check. Minimum Qualifications Bachelor's degree; at least 3 years of experience directly related to the duties and responsibilities specified. Completed degree(s) from an accredited institution that are above the minimum education requirement may be substituted for experience on a year for year basis. Preferred Qualifications Experience with community-engaged research. Experience working with rural communities in New Mexico. Experience with nutrition education. Firm understanding of research methods, protocols, procedures and techniques in social marketing. Background in public health. Written and oral strong interpersonal and communication skills and the ability to work effectively with a wide range of individuals in diverse communities. Additional Requirements Campus Health Sciences Center (HSC) - Albuquerque, NM Department Peds Prvn and Population Sciences (997E) Employment Type Staff Staff Type Term - Full-Time Term End Date 9/30/2025 Status Exempt Pay Monthly: $3,697.20 - $5,191.33 Benefits Eligible This is a benefits eligible position. The University of New Mexico provides a comprehensive package of benefits including medical, dental, vision, and life insurance. In addition, UNM offers educational benefits through the tuition remission and dependent education programs. See the Benefits home page for a more information. ERB Statement As a condition of employment, eligible employees working greater than .25 FTE as determined by the New Mexico Education Retirement Act must make mandatory retirement contributions. For more information, review the Benefits Eligibility at a Glance grid. Background Check Required Yes For Best Consideration Date 1/24/2025 Eligible for Remote Work Yes Eligible for Remote Work Statement This position is eligible for a remote/hybrid schedule. Application Instructions Only applications submitted through the official UNMJobs site will be accepted. If you are viewing this job advertisement on a 3rd party site, please visit UNMJobs to submit an application. A complete application will consist of complete on-line application (include hours worked for each position), current resume, cover letter and references. Please describe in your cover letter how you meet the preferred qualifications for the position. Attach three professional references, preferably supervisors including name and contact information. Positions posted with a Staff Type of Regular or Term are eligible for the Veteran Preference Program. See the Veteran Preference Program webpage for additional details. The University of New Mexico is committed to hiring and retaining a diverse workforce. We are an Equal Opportunity Employer, making decisions without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, veteran status, disability, or any other protected class. The University of New Mexico requires all regular staff positions successfully pass a pre-employment background check. This may include, but is not limited to, a criminal history background check, New Mexico Department of Health fingerprint screening, New Mexico Children, Youth, and Families Department fingerprint screening, verification of education credentials, and/or verification of prior employment. For more information about background checks, visit ********************************************************** Refer to ********************************************************* for a definition of Regular Staff.

At Perrigo, we are driven by our mission to Makes Lives Better Through Trusted Health and Wellness Solutions, Accessible to All. We are proud to be a Top 10 player in the European Consumer Self-Care market and the largest U.S. store brand provider of over the counter and infant formula. Dedicated to providing The Best Self-Care for Everyone, we are the people behind the brands you trust. We are Opill, Compeed, Solpadeine, NiQuitin, ACO, and many more. We Are Perrigo. We are committed to enhancing the wellbeing of our colleagues and consumers alike. We pride ourselves on fostering an inclusive, collaborative culture where each person can experience a sense of belonging. Join us on our One Perrigo journey as we evolve to a blended-branded business to win in self-care. Description Overview Looking for talented individuals who are passionate about developing different effective, stable, and robust drug products with hands-on and applied work experience with oral solids and liquids, and topicals (semi-solids) dosage forms who thrive in collaborative environments and are driven by curiosity, innovation and scientific excellence, ensuring that each product meets the highest standards of quality and efficacy. This position requires a deep understanding of pharmaceutical and material sciences, chemistry, and biology as well as the creativity to design and optimize dosage forms to receive consideration for this role. Scope of the Role * Conduct formulation research via quality scientific experimentation to create new products that meet quality and efficacy standards that comply with industry regulations and guidelines. * Support troubleshooting and help in resolving formulation-related issues. * Generate and maintain accurate and reliable scientific data from designed experiments by following established procedures and practices to support product development. * Analyze and defend scientific data from experiments and prepare reports on formulation performance. * Perform effective problems solving, resolution, and implementation of process improvements in designated day-to-day operations and participate in large scope product/process development and improvement projects. * Prepare and/or Review internal/external Master Batch Records for Experimental, Pilot/Pivotal, scale-up and process validation batches. * Communicate formulation development findings effectively to project manager and the wider development team and presents data at team meetings and departmental technical meetings. * Collaborate with multidisciplinary (local and global) teams to resolve complex product development issues and respond to internal and external audits. * Provide technical support to Technical Operations, Manufacturing, Packaging, Quality and others, internally and/or at third party contractors. * Partner with marketing and internal consumer research teams to support front end innovation, consumer research studies to optimize product design and assure new products deliver an exceptional consumer experience. Experience Required * At a minimum, a Bachelor's degree in Pharmaceutical Sciences or related life-sciences * 2+ years of experience in formulation or product development. * Understanding of Good Manufacturing Practices (GMP). * Excellent problem-solving skills. * Knowledge in PK and BE designs * Effective communication and presentation skills (project management abilities, time management and organizational skills are a plus) * Knowledge of analytical testing techniques. * Ability to work in a team environment. * Familiarity with regulatory guidelines and compliance. * Detail-oriented with strong documentation skills. * Ability to troubleshoot and resolve technical issues. * Sound knowledge of pharmaceutical excipients and raw materials. Benefits We believe our people are our greatest asset. Alongside competitive compensation, we offer benefits tailored to supporting you and your family, as well as career development opportunities to ensure you feel valued and supported, both professionally and personally. Find out more about Total Rewards at Perrigo. Hybrid Working Approach We love our offices and the setting they provide for in-person collaboration and celebration. But we also appreciate the opportunity to work remotely can energise you too, so we promote flexibility with the ability to work two days a week from home in many roles. We are proud to be included in the Forbes list of "America's Best Employers by State 2024". Find out more here Applicants please note: To apply to this position please click the APPLY button at the bottom of the application. (The SAVE button will only save your profile information but not submit an application for this open position.) Thank you. We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or other characteristics protected by law. #weareperrigo Nearest Major Market: Grand Rapids

The Microbiology Scientist I will conduct various bench testing procedures, including sample preparation, plating, culturing, and environmental swabs, monitoring, and testing. This role involves conducting microbial and physical analyses to support the development of manufacturable multisource pharmaceutical products. The scientist will provide analytical support for the release of registration materials in support of regulatory submissions and assist in analytical method validation and transfer activities. Responsibilities * Perform assigned analytical tasks in support of product development, registration lot release, and pre- and post-regulatory submission activities. * Conduct activities within assigned timelines while complying with cGXP's, and company practices and procedures. * Follow work instructions, SOPs, and company practices. * Document analytical activities and results accurately, in a timely manner, and maintain data integrity. * Identify execution challenges of analytical methods and support troubleshooting activities. Essential Skills * Experience in microbiology lab techniques and procedures. * Experience with dilutions, sample preparation, biochemistry, and quality control. * Bachelor's degree in Microbiology or Biology with a minor in Microbiology. * Ability to work in a team environment to accomplish assigned tasks. * Capability to handle multiple tasks in a fast-paced environment. * Good written and verbal communication skills. * Ability to work with supervision using scientific judgment and professional competency. Additional Skills & Qualifications * Strongly prefer candidates with lab experience outside of academia in a microbiology lab/testing environment. * Must have a Bachelor of Science in Microbiology or Biology with a minor in Microbiology Pay and Benefits The pay range for this position is $24.00 - $24.00 Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: * Medical, dental & vision * Critical Illness, Accident, and Hospital * 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available * Life Insurance (Voluntary Life & AD&D for the employee and dependents) * Short and long-term disability * Health Spending Account (HSA) * Transportation benefits * Employee Assistance Program * Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Columbus,OH. Application Deadline This position will be accepting applications until Feb 7, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. Diversity, Equity & Inclusion At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through: * Hiring diverse talent * Maintaining an inclusive environment through persistent self-reflection * Building a culture of care, engagement, and recognition with clear outcomes * Ensuring growth opportunities for our people The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

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

We are seeking a highly skilled and dedicated Carbon Forest Scientist with a Ph.D. in Forestry, Environmental Science, or a related field, and significant experience in the carbon markets. The ideal candidate will have a strong background in conducting rigorous scientific research and a proven track record of working with NGOs or similar organizations to influence environmental policy and practices.What You'll Be Doing Conduct high-level research on forest carbon dynamics, including carbon sequestration, emission reduction, and overall forest health. Develop and oversee projects aimed at enhancing carbon storage in forests, considering biodiversity conservation and sustainable community development. Analyze data using advanced statistical and GIS tools to monitor forest carbon stocks and changes over time. Collaborate with policy makers, community leaders, and international bodies to advocate for effective forest conservation strategies based on research findings. Write grant proposals, scientific papers, and reports to secure funding and share research outcomes with the scientific community and the public. Lead field teams in data collection, ensuring adherence to safety and ethical standards. Engage with stakeholders in the carbon markets to apply practical insights from research to market-based solutions. What You'll Need Degree in Forestry, Environmental Science, Ecology, or related field. Minimum of 5 years of relevant experience in carbon markets, forest conservation, and climate change mitigation. Proficiency in statistical analysis, GIS, and remote sensing tools. Demonstrated ability to publish peer-reviewed research and secure research funding. Strong leadership skills and experience managing diverse teams. Excellent communication and interpersonal skills, with the ability to engage effectively with a wide range of stakeholders. $100,000 - $150,000 a year Candidates for this role must be located in the United States.

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.

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.

JOB TITLE: AI Scientist REPORTS TO: Lead Applied AI Scientist DEPARTMENT: Finetune Development Prometric is transforming the assessment industry through innovative AI solutions, including its acquisition of Finetune. Finetune's R&D and product team combined innovative thinking in teaching and learning with expertise in leading-edge technology for more than ten years and has been a pioneer in the Large Language Model application in education space. Our work includes Generate and Catalog-products that use a unique, patent-pending AI approach to help author and tag content at scale. Finetune is also created AP Classroom-a platform we built in partnership with The College Board that serves over 3 million students and 175,000 teachers daily. We've assembled a global team representing more than a dozen countries, working together in a fully remote, intellectually vibrant culture that values collaboration, communication, and the diversity of perspective our members bring to the company. Salary for this role is starting at $150,000. COMPANY BACKGROUND Prometric (****************** is a trusted test development and delivery provider to more than 300 organizations worldwide. Prometric serves as an industry gatekeeper, ensuring that people legitimately earn the credentials they seek to achieve, and thereby guaranteeing a fair testing experience for all who come through our doors. RESPONSIBILITIES * This is not a standard data science role with clean datasets and predetermined train-test splits. You will develop custom AI solutions in a dynamic environment where requirements evolve and data is often unstructured. Your responsibilities will include: * Designing and implementing AI systems for intelligent content generation and classification in educational assessment * Building customized AI solutions to meet specific customer requirements * Conducting rapid technical investigations and lightweight research * Creating production-ready AI pipelines that integrate with our product ecosystem * Developing internal tools to automate and enhance team efficiency QUALIFICATION REQUIREMENTS * Bachelor's degree with 5+ years of relevant experience or Master's degree with 2+ years of real-world work experience * Strong Python programming skills * Comfort with collaborative development practices, specifically Git and code review * Practical experience implementing solutions using LLM APIs * Demonstrated ability to work effectively with ill-defined requirements and independently lead projects * EXPERIENCE AND SKILLS * Strong customer empathy with ability to "channel the customer" in solution design * Product mindset-you go beyond data analysis, doing work that directly shaped user-facing features * Experience communicating directly with customers PHYSICAL JOB REQUIREMENTS * N/A

Major Responsibilities : Responsible for implementing and maintaining the effectiveness of the quality system. · Weighs ingredients, prepares batches, and supports production at the product research center · Submits samples for analysis and consolidates/tabulates results · Organizes non-routine testing, completes these tests and summarizes results B.S. in Food Science and Technology, Chemistry or Sciences preferred. 0 - 3 years technical work experience, preferably in developing food/nutritional products The candidate should also demonstrate the ability to handle multiple priorities as well as a good work ethic Qualifications B.S. in Food Science and Technology, Chemistry or Sciences preferred. 0 - 3 years technical work experience, preferably in developing food/nutritional products Additional Information Thanks & Regards ________________________________________________________________________ ___ Riya Seth | Team Recruitment | Mindlance, Inc. | W: ************

We're looking for a Senior Industry Consultant to support Procore's Account Executive and Sales Engineering teams, serving as a trusted resource throughout the sales process. In this highly collaborative role, you'll supplement the sales process with technical knowledge of powerful platform capabilities and key partner solutions for the GC audience. You'll assist with business process discovery, provide technical answers and resources related to Procore platform functionality, audience trends, and partners. This position will report to our Sales Solutions leadership, and has the opportunity to be based out of any of our US offices or remotely within the US. We're looking for someone to join our team immediately. What you'll do: Drive platform and partner sales by strategically aligning to opportunities with specific segments and audiences Educate prospects on their maturity compared to peers by staying in tune with current trends related to your audience Partner with Account Executives and Sales Engineers to map business processes to show the value of the Procore platform and partners Visit with clients where the account team has identified a risk of churn. You'll visit with those clients, both in offices and job sites as you deem fit. Propose action plans to mitigate churn identified above using other Procore resources (IE: CSEs, SPCs, and AMs) Work with the Partner team to identify, design, receive and utilize new partners and integrations strategically within opportunities Support the Partner team with scoping and mapping of strategic partnerships and integrations Become a Procore expert on key platform functionality such as customization, configuration options, permission management, and more Visit the job sites of existing or potential partners to review their current processes and needs. Present discovery documentation to internal and external teams. Usually in the form of Google Slide presentations. Rely on your construction experience to tell stories that weave Procore's functionality into best practices for our new and existing clients. Craft and post articles/videos to LinkedIn and other social media that celebrate Procore wins and product releases What we're looking for: 15+ years of experience working within the construction OR construction tech industry Experience working with Enterprise and Strategic clients to understand complex business objectives and challenges Ability to coordinate across Revenue teams to guide strategy and prioritization for strategic partner needs and advancement of deals Knowledge and experience in scaling processes around a Procore ecosystem, discovery, solution selling, etc. Passion for finding the best solution for clients with a combination of Procore and partner solutions; demonstrated success in presenting solutions alongside partners to meet client needs Strong presentation skills and ability to engage in technical discussions and discovery General knowledge of Procore's API and a basic understanding of how integrations are created and managed Experience using the Procore platform is highly preferred Technology evangelists with a passion for modernizing the construction industry are highly preferred Additional Information Base Pay Range $73 - $100 plus commission for an estimated on-target earnings of $216,089 - $297,122. This role is also eligible for Equity Compensation. Procore is committed to offering competitive, fair, and commensurate compensation, and has provided an estimated pay range for this role. Actual compensation will be based on a candidate's job-related skills, experience, education or training, and location. Perks & Benefits At Procore, we invest in our employees and provide a full range of benefits and perks to help you grow and thrive. From generous paid time off and healthcare coverage to career enrichment and development programs, learn more details about what we offer and how we empower you to be your best. About Us Procore Technologies is building the software that builds the world. We provide cloud-based construction management software that helps clients more efficiently build skyscrapers, hospitals, retail centers, airports, housing complexes, and more. At Procore, we have worked hard to create and maintain a culture where you can own your work and are encouraged and given resources to try new ideas. Check us out on Glassdoor to see what others are saying about working at Procore. We are an equal-opportunity employer and welcome builders of all backgrounds. We thrive in a diverse, dynamic, and inclusive environment. We do not tolerate discrimination against candidates or employees on the basis of gender, sex, national origin, civil status, family status, sexual orientation, religion, age, disability, race, traveler community, status as a protected veteran or any other classification protected by law. If you'd like to stay in touch and be the first to hear about new roles at Procore, join our Talent Community . Alternative methods of applying for employment are available to individuals unable to submit an application through this site because of a disability. Contact our benefits team here to discuss reasonable accommodations. For Los Angeles County (unincorporated) Candidates: Procore will consider for employment all qualified applicants, including those with arrest or conviction records, in accordance with the requirements of applicable federal, state, and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance, the Los Angeles County Fair Chance Ordinance for Employers, and the California Fair Chance Act. A criminal history may have a direct, adverse, and negative relationship on the following job duties, potentially resulting in the withdrawal of the conditional offer of employment: 1. appropriately managing, accessing, and handling confidential information including proprietary and trade secret information, as well as accessing Procore's information technology systems and platforms; 2. interacting with and occasionally having unsupervised contact with internal/external customers, stakeholders, and/or colleagues; and 3. exercising sound judgment.

Reports To: COO Job Type: Full time, Exempt Anticipated Schedule: 4 days a week, 8 hours per day, Monday - Thursday (Hybrid) As a pioneering woman-owned business founded in 2014, Bicycle Transit Systems leads the way in bike share program management nationwide - we are the only vertically integrated bike share provider overseeing the customer experience from product design to local implementation and operation. Our mission is to strengthen communities and protect our planet through the development and implementation of bike share. At Bike Transit, we foster a culture of collaboration, innovation, and environmental stewardship. We are passionate about providing safe, seamless, reliable, and memorable customer experiences, building mutually-rewarding relationships with our riders, suppliers, and clients. We are currently seeking a Decision Scientist to solve complex business challenges by leveraging a variety of quantitative methods to identify and solve problems. They will create and apply advanced analytical approaches to optimize processes, guide decision-making, and provide data-driven insights to shape business strategy and operations. This role is for someone who is excited about solving problems, thinks critically, adapts to challenges, and applies the best methods to deliver impactful solutions. A few of the benefits we offer: Competitive compensation package Affordable medical, dental, and vision insurance options 401k with up to 4% employer match 4-Day work week 3 weeks PTO + 1 week sick time off per year Paid parental leave Essential Duties and Responsibilities: Solve exciting and complex business challenges, including station siting optimization, demand forecasting, fraud detection, maintenance prediction, resource allocation, and more. Leverage large datasets, statistical techniques, and hypothesis testing to produce actionable recommendations. Use quantitative analysis to understand key drivers of business performance, system dynamics, and long-term trends. Develop and implement decision-making and predictive models, and advanced analytical techniques such as optimization, machine learning, and simulation. Design and implement experiments to test hypotheses. Collaborate with cross-functional teams to implement, document, validate and monitor the impact of decisions Work with business and product leaders to define key metrics and provide insights that support strategic goals. Mentor junior analysts on advanced methods, problem-solving approaches, and best practices in analytics. Lead and manage small Data Team, including evaluating performance, providing regular feedback, holding regular one-on-one check-ins, and conducting performance reviews. Currently the Team has one Data Analyst. Create reports, dashboards, and ad hoc analyses to support business decision-making. Communicate findings to stakeholders in a clear and concise manner, often through visual reporting tools Partner with business analysts, field personnel, and cross-functional teams to identify challenges and develop data-driven solutions. Collaborate with engineering team to manage data logistics - including data specifications, transfers, structures, and rules. Take a proactive, independent role in project design, planning & execution. Stay abreast of industry trends and innovations in data science and analytics Work closely with software engineers to guide the design and optimization of database structures and data pipelines, ensuring they meet analytical requirements and uphold data integrity Other duties as assigned Education and/or Work Experience Requirements: Education & Experience: Master's, PhD, or equivalent experience in Statistics, Operations Research, Mathematics, Computer Science, Economics, Engineering, or a related quantitative field. 3+ years of experience in data analysis, business intelligence, operations research, or a related quantitative role. Technical Skills: Fluency in SQL for data extraction and manipulation. Fluency with programming languages such as R or Python for statistical analysis and modeling. Proficiency in data visualization tools like Tableau, Power BI, or similar platforms. Expertise in advanced analytics techniques, including predictive modeling, machine learning, optimization, simulation, and statistical methods. Experience working with big data. Business & Problem-Solving Skills: Ability to translate complex data findings into actionable insights for business product teams and executive leadership. Experience in decision science, system dynamics, or strategic modeling to inform business operations. Strong problem-solving skills with a focus on structured analytical thinking and attention to detail. Ability to work independently, manage multiple projects, and take ownership of analysis and recommendations. Collaboration & Communication: Strong written and verbal communication skills, with the ability to present data-driven insights to both technical and non-technical audiences. Ability to collaborate with engineering teams on data logistics, specifications, and infrastructure. Experience working cross-functionally with business analysts, operations teams, and field personnel to address challenges and improve decision-making. Physical Requirements and Special Demands (The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job.): Ability to maintain regular, punctual attendance in accordance with company and department policy. Repetitive motion required of the wrists, hands, or fingers occasionally throughout the workday. Must be able to talk, listen and speak clearly on telephone throughout the workday. Any travel would be primarily local during the business day. Work from home shifts require a reliable internet connection and an environment to take calls where quiet & customer privacy can be assured. This role routinely uses standard office equipment such as computers, phones, and photocopiers. Must be able to lift up to 20lbs. Riding a bikeshare bike, occasionally out on the field or in the warehouse. This role requires the ability to speak clearly so listeners can understand, understand the speech of another person, see details of objects that are less than a few feet away, stand or sit for several hours straight at a time, and bend or stoop as necessary. This is a full-time, hybrid position expected to work 32 hours per week (4 days per week, 8 hours per day). Some hours outside of this, including nights and weekends, may be required. We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law. Equal Opportunity Employer M/F/V/D

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-TG1 This 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.