Certifying scientist remote jobs are in high demand as laboratories and biotech companies across the United States expand their quality assurance teams. With 216 open positions available, this is an excellent opportunity for professionals who thrive in independent, detail-oriented environments. Companies nationwide are embracing remote certifying scientist jobs to access top talent regardless of location.
Successful candidates typically bring strong backgrounds in analytical chemistry, microbiology, or quality control, paired with experience interpreting regulatory standards such as GMP and FDA guidelines. Employers seeking to hire a certifying scientist often prioritize meticulous documentation skills, sound judgment in batch release decisions, and familiarity with laboratory information management systems. Strong communication abilities are equally valuable for collaborating with cross-functional teams.
Remote work in this field has become increasingly common as digital documentation and electronic batch records streamline quality verification. Companies across the USA now offer flexible, home-based arrangements that allow experienced professionals to review data and sign off on certifications without daily lab commutes. This shift reflects a broader industry trend, with certifying scientist vacancies appearing across pharmaceutical, biotechnology, and food safety sectors nationwide.
If you are ready to take the next step in your career, now is the time to explore certifying scientist positions that match your expertise. Global Work AI connects skilled professionals with employers seeking qualified candidates for remote roles across the country. Discover how your experience can make an impact and find the right opportunity today.
Premier Research
Review medical data including labs, patient profiles, and CRF data. Support the setup and documentation of project-specific medical monitoring requirements. Develop and review medical monitoring plans and assist Medical Directors with monitoring activities.
remote, United States$81k/yrFull TimeJunior (<2 years)
University of Virginia
Oversee the Hematology & Oncology Lipidomics Facility, ensuring proper instrument usage and maintenance. Develop and modify protocols for small molecule analyses, liaise with facility users for experimental needs, and provide training to laboratory personnel.
remote, WY, United StatesPart TimeLead / Manager
Telix Pharmaceuticals (AMER)
Provide technical and analytical expertise for biologics process development and manufacturing. Manage projects at external CDMO partners, ensuring compliance with safety standards and regulatory expectations.
remote, United StatesFull TimeSenior (5+ years)
Elanco
Guide the global regulatory strategy for development projects, focusing on CVM/FDA submissions. Serve as the regulatory subject matter expert on project teams, providing risk/benefit evaluations. Lead engagements with regulatory agencies, including pre-submission meetings and negotiations.
remote, IN, United States$118k – $197k/yrFull TimeSenior (5+ years)
MSD
Develop and oversee global regulatory strategies for companion diagnostics and IVD products. Manage regulatory activities related to development, registration, and lifecycle management of diagnostic products.
remote, United States$232k – $365k/yrFull TimeLead / Manager
RTI International
Lead drug policy work, providing clinical oversight for evidence-related tasks. Conduct rapid comparative effectiveness reviews, ensuring rigorous methods and timely delivery. Oversee clinical review and quality control of deliverables, including data extraction and synthesis of findings.
remote, United States$166k – $206k/yrFull TimeSenior (5+ years)
Critical Path Institute (C-Path)
Provide scientific leadership and technical support for the NAMs portfolio, including the NAMs Developer Coalition. Evaluate NAM technologies, develop validation strategies, and support regulatory submissions.
remote, United StatesFull TimeDirector
Danaher Corporation
Conduct applications support for automation and liquid handling products, adapting workflows to customer needs. Assess customer projects, develop and optimize protocols, and troubleshoot technical issues.
remote, IA, United States$95k/yrFull TimeJunior (<2 years)Danaher Corporation
Execute daily production plans ensuring due date conformance and quality standards. Independently perform mammalian cell culture tasks while adhering to Standard Operating Procedures (SOPs).
remote, United States$56k – $65k/yrFull TimeJunior (<2 years)
J.S. Held LLC
Lead complex environmental investigations and inspections related to hazardous materials. Manage field activities, including sampling programs, ensuring compliance with regulations. Oversee environmental data interpretation and prepare technical reports with recommendations.
remote, CA, United States$110k – $165k/yrFull TimeSenior (5+ years)
Oregon Tilth
Review applications for certification, inspection reports, and mid-year requests. Issue certification decisions and provide technical assistance to clients. Collaborate with inspectors and certification staff to ensure compliance and timely service delivery.
remote, United StatesFull TimeMiddle (2-4 years)
CHN Nebraska
Lead and oversee scientific aspects of research and evaluation projects, including proposal development, research design, and data analysis. Develop project workplans, measurement tools, and deliverables. Conduct qualitative data collection and ensure data integrity.
remote, United StatesFull TimeJunior (<2 years)
SGS
Perform third-party social compliance audits according to SGS Certification procedures. Control and oversee audit teams, ensuring efficient audit processes. Analyze information to recommend certification and maintain audit-related credentials.
remote, United States$90k – $120k/yrFull TimeSenior (5+ years)
Columbus
Conduct scientific evaluations of R&D landscapes to identify research gaps. Monitor progress toward established metrics and develop briefings for diverse audiences. Support the development and management of R&D programs, including administrative tasks like analyzing and writing reports.
remote, United States$121k – $210k/yrFull TimeSenior (5+ years)
PENNSYLVANIA CERTIFIED ORGANIC
Lead the Certification Review Team, overseeing certification workflow and ensuring compliance with USDA organic standards. Manage team performance, conduct reviews, and implement certification policies. Foster a collaborative team culture and support staff development through coaching and mentoring.
remote, PA, United States$78k – $107k/yrFull TimeLead / ManagerFaro
Provide clinical and scientific leadership across product development. Define clinical frameworks and evidence models for Faro’s tools. Collaborate with product and data science teams to design algorithms and decision-support features.
remote, CA, United States$170k – $200k/yrFull TimeLead / Manager
Rochester Regional Health
Support relationships with global Referral Laboratories, ensuring service delivery aligns with Clinical Trial requirements. Maintain and enter laboratory information in databases, assist with work orders, and track communications.
remote, Rochester, NY, United States$46k – $56k/yrFull TimeJunior (<2 years)Columbus Technologies and Services
Conduct scientific evaluations of R&D landscapes to identify research gaps, monitor progress towards metrics, and develop briefings for diverse audiences. Support the development and management of R&D programs, including administrative tasks like analyzing and writing reports.
remote, United StatesFull TimeSenior (5+ years)
CSL
Provide expert technical assessment and scientific guidance for CMC activities in biologics, focusing on process development, analytical development, and technology transfer. Develop data-driven recommendations balancing scientific rationale and regulatory expectations.
remote, Waltham, MA, United States$179k – $212k/yrFull TimeSenior (5+ years)
Promega
Conduct validation studies for Promega instruments and chemistries in forensic DNA laboratories. Analyze data, write reports, and train lab staff on new systems. Present validation programs and provide expert technical solutions throughout the validation process.
remote, United StatesFull TimeMiddle (2-4 years)
Kumquat Biosciences Inc
Oversee clinical data review and analysis to ensure integrity and support safety assessments. Develop and execute clinical development plans, protocols, and amendments. Contribute to clinical and regulatory documents, manage vendor relationships, and ensure compliance with GCP/GVP guidelines.
remote, San Diego, CA, United StatesFull TimeDirector
Volga Partners
Evaluate AI-generated pharmaceutical content for accuracy and completeness. Review information related to formulation, process development, and manufacturing science. Analyze scientific reasoning and identify errors or inconsistencies in AI-generated conclusions.
remote, United States$40k – $101k/yrPart TimeMiddle (2-4 years)
Galvanize
Provide scientific and writing support for clinical strategy, trial development, and data analysis. Conduct critical reviews of clinical documents and collaborate with internal and external stakeholders.
remote, United States$145k – $165k/yrFull TimeSenior (5+ years)
Getinge
Design and validate sterilization programs for medical devices, ensuring compliance with global regulatory standards. Author and execute protocols and validation reports, manage microbial barrier testing, and provide technical support for existing products.
remote, United States$99k – $135k/yrFull TimeMiddle (2-4 years)
CCOF
Provide technical services to certified organic processor/handler clients, including reviewing updates on labels, formulations, and compliance with USDA NOP standards. Make compliance decisions and communicate them to clients.
remote, United States$58k – $62k/yrFull TimeMiddle (2-4 years)
Arcus Biosciences
Conduct clinical studies with cross-functional teams, focusing on operational feasibility, data management, and communication plans. Support medical monitoring, safety reviews, and data analysis for clinical trial data.
remote, CA, United States$165k – $180k/yrFull TimeJunior (<2 years)
Altasciences
Perform macroscopic and microscopic evaluations of tissue samples, supervise necropsies, and guide staff in sample collection. Write detailed reports on test article effects and enter findings into data systems.
remote, Columbia, MO, United States$170k – $210k/yrFull TimeLead / Manager
Maine Organic Farmers and Gardeners Association
Conduct technical reviews of organic system plans and inspection reports, ensuring compliance with USDA National Organic Program standards. Perform inspections and pesticide residue sampling as time allows. Maintain organized client files and pursue adverse actions in coordination with colleagues.
remote, MA, United States$50k – $55k/yrFull TimeJunior (<2 years)
SecureBio
Conduct capability and safeguard assessments of emerging AI models, executing evaluation pipelines and analyzing data to identify risks. Manually assess models for biological knowledge and willingness, synthesizing findings into evaluation reports and risk summaries.
remote, United States$235k – $300k/yrFull TimeSenior (5+ years)IIIIIIUS
Plan, organize, and perform technical aspects of solicitation and peer-review activities. Identify and recruit qualified reviewers, manage conflict-of-interest processes, and advise government stakeholders on panel operations.
remote, DC, United States$90k – $152k/yrFull TimeSenior (5+ years)Maine Organic Farmers and Gardeners Association
Conduct technical reviews of organic system plans, primarily for livestock and dairy. Review inspection reports and communicate results to producers. Perform inspections, residue sampling, and investigate complaints to uphold organic certification integrity.
remote, MA, United States$50k – $55k/yrFull TimeJunior (<2 years)
Canacre USA, LLC
Conduct field surveys to assess wetlands and watercourses, collect data on ecological health, create maps using GIS technology, ensure regulatory compliance, evaluate habitats, participate in restoration projects, monitor wetland health, and educate the public about ecosystem sustainability.
remote, FL, United StatesFull TimeMiddle (2-4 years)
Abbott
Support clinical curation of databases and multi-gene panels, ensuring compliance with professional guidelines. Collaborate with laboratory teams to maintain clinical information streams and support phenotype-driven testing products.
remote, WI, United States$61k/yrFull TimeJunior (<2 years)
Advarra
Ensure compliance with regulatory requirements and Advarra’s Standard Operating Procedures. Assist in the triaging and review of submissions for expedited or full board review.
remote, United States$58k – $97k/yrFull TimeMiddle (2-4 years)
Unchained Labs
Conduct pre-sales technical presentations and seminars, plan and execute demonstrations of analytical instruments, and maintain expert-level knowledge of the product line. Provide post-sales account development support, install and QC instruments, and train customers and distributors.
remote, United States$110k – $135k/yrFull TimeSenior (5+ years)BlueRidge Life Sciences
Oversee study design, data interpretation, and monitoring of toxicology studies. Write and review pharmacology/toxicology sections of regulatory documents and interact with regulatory agencies.
remote, NJ, United StatesFull TimeSenior (5+ years)
AECOM
Lead wetland field delineations in Connecticut and adjacent states. Prepare wetland technical reports and environmental permit applications. Collaborate with a team of professionals on projects in energy transmission and generation sectors, including electric transmission, renewables, and storage.
remote, CT, United States$75k – $117k/yrFull TimeLead / Manager
Cortek Inc
Serve as a technical expert in laboratory operations, resolving system issues and developing plans for complex systems. Manage multicenter studies and short-term testing activities, ensuring proper implementation of programs.
remote, Arlington, VA, United StatesFull TimeSenior (5+ years)
ICF
Plan, organize, and perform technical aspects of solicitation and peer-review activities. Identify and recruit qualified reviewers, manage conflict-of-interest processes, and advise government stakeholders on panel operations.
remote, DC, United States$90k – $152k/yrFull TimeSenior (5+ years)
Praxis Precision Medicines, Inc.
Lead analytical development strategies for small molecule drug substances and products. Oversee method development, qualification, validation, and GMP testing activities.
remote, United States$170k – $190k/yrFull TimeLead / Manager10,000,000+ more jobs available!
