Regulatory Scientist & GLP Study Director, Env Fate
$121k - $157kValent U.S.A. LLC
Valent U.S.A. LLC is seeking a Regulatory Scientist in San Ramon, California. This role involves serving as GLP Study Director, managing environmental fate studies, and leading a team of Chemists. The ideal candidate will have a strong background in regulatory submissions, mentoring, and deep expertise in chromatography. The position offers a competitive salary of $121,000 to $157,000 annually and benefits starting day one. #J-18808-Ljbffr Valent U.S.A. LLC
$121k - $157k
...protection company located in California is seeking a Regulatory Scientist to lead regulatory studies and mentor scientific staff. The ideal candidate will... ...MS or PhD in Chemistry and significant experience in GLP guidelines and regulatory submissions. Responsibilities...Regulatory$121k - $157k
...renewable resource. General Description: The Regulatory Scientist serves as a senior scientific leader and GLP Study Director, providing strategic and technical oversight... ...-ready, scientifically sound environmental fate and metabolism studies. The position shapes study...RegulatoryFull timeContract workImmediate startLong distance$123k - $163k
...Principal Scientist 1 – Hayward, CA Meadowhawk Biolabs is seeking... ...Scientist to work within the non-GLP Immunoanalytical Services... ...of standard and non-standard study designs, execution, analysis,... ...development of and adhere to company regulatory and good science procedures...RegulatoryContract workWork at office- ...are seeking a Senior Scientist, DMPK, to join our R&D... ...Reporting to the Senior Director, DMPK, this individual... ...‑of‑concept clinical studies. This is a great opportunity... .../DMPK, and prepare regulatory submission... ...Expertise managing CROs, GLP, and other regulated activities...RegulatoryFlexible hours
$40 per hour
...This is a hands-on, bench-based scientist role primarily responsible... ...technical performance chapters for regulatory dossiers, ensuring compliance... .... Main Responsibilities: •Study Design & Execution: Design... ...Controls, ISO standards, cGMP, GLP, and Good Documentation...RegulatoryHourly payPermanent employmentFull timeMonday to FridayShift workDay shift- ...CRO providing global-standard services in GLP/GCLP bioanalysis and biomarker. Our... ...for interaction with the client from the study design to scheduling, conducting, reporting... ...Discovery (ECL)). Author and/or review key regulatory documents, validation plans and reports,...Regulatory
$106.28k - $188.96k
...project delivery, permitting/regulatory coordination, and implementation... .... Our engineers, scientists, technical and project employees... ..., source identification, and fate and transport considerations.... ...recommendations. Oversee pilot studies and full‑scale PFAS remedy implementation...RegulatoryFor contractorsFor subcontractorWork at officeLocal areaNight shift$177.5k - $251.5k
...data for key clinical and QA metrics. Review and approve deviations and corrective and preventive actions (CAPAs). Partner with regulatory affairs, clinical operations, and translational medicine to address compliance issues and provide guidance. Maintain knowledge of...RegulatoryLocal areaFlexible hours- ...Principal Scientist Company is developing a novel, single molecule Next Generation Sequencing platform that aims to... ...Development, Manufacturing/Operations, Quality, Marketing, Regulatory Affairs, Clinical Studies, Bioinformatics and International Technical Services),...Regulatory
- ...modified microorganisms, development of analytical methods, scale‑up studies utilizing external resources, and evaluation of new enzyme-... ...R&D projects under the direction of the supervisor, including regulatory requirements, scientific literature, technical journals,...Regulatory
- ...hiring an Environmental Noise Scientist (CG06) to perform... ...TNM and SoundPLAN, evaluating regulatory thresholds, and drafting high... ...will report to the Associate Director of Air & Noise. Education and... ...stand-alone noise technical studies in compliance with CEQA Duties...RegulatoryWork at officeLocal areaHome office
- ...Biosciences is seeking a Senior Clinical Research Scientist II in Berkeley, California, to lead the... ...across teams and oversight of study execution, ensuring high-quality data generation... ...and CAR-T therapy, enabling effective regulatory submissions and scientific contributions...RegulatoryRemote work
- ...Candidates should have a Ph.D. or equivalent in a relevant field and substantial industry experience in GLP/GCLP bioanalysis. The position emphasizes client interaction, regulatory document authoring, and operational excellence, fostering an inclusive and committed workplace....Regulatory
- Exelixis, Inc. seeks Scientist III (Biologics Drug Product Development) in Alameda, CA. Duties... ...records up to date. Design and execute studies in‑house. Perform biophysical... ...current with journal articles and changing regulatory requirements regarding analytical testing...RegulatoryContract work
$177.5k - $251.5k
...activities. Reviews and approves Deviations, and Corrective and Preventive Actions (CAPAs) Partners with other groups including Regulatory Affairs, Clinical Operations, Translational Medicine, regarding compliance issues and provides compliance guidance Maintains knowledge...RegulatoryLocal areaFlexible hours$100k - $125k
Summary The R&D Scientist will lead the development and commercialization of innovative nutraceutical... ...improvement, technical presentations, regulatory documentation, shelf‑life testing,... ...label reviews. Coordinate shelf‑life studies, prototype development, and commercialization...Regulatory$24 - $50 per hour
...collaboratively with other Dudek staff and subconsultants to conduct field studies/surveys, including but not limited to the following:... ...pursuant to federal and state requirements to support regulatory permit applications Record and take notes of any observations...RegulatoryHourly payPart timeWork at officeRemote workLong distance$111k - $206.5k
...highly motivated and experienced IHC senior scientist with a strong histology/pathology... ...sensitivity, reproducibility, and robustness studies.* Utilize orthogonal methods (e.g.,... ...functionally with R&D, pathology, operation, and regulatory teams.* Contribute to scientific...RegulatoryRelocation package$50 - $60 per hour
...instrumentation and techniques, and a strong understanding of the regulatory and technical landscapes in the biotech or food & beverage... ...and Manufacturing. Ensure laboratory operations comply with GLP/GMP standards and safety protocols. Support method transfer,...Regulatory- ...an experienced, highly quantitative scientist to lead bioanalytical strategy and quality... ...data Working knowledge of GLP bioanalysis and regulatory expectations (e.g., ICH M10) Solid... ...Experience supporting IND-enabling studies or clinical programs Familiarity...Regulatory
$120k - $165k
...Pleasanton, CA seeking a Sr. Scientist or Associate Principal... ...Development, Method Validation, GLP/GCLP Bioanalysis for PK, and... ...interaction with the client from the study design to scheduling,... ...Author and/or review key regulatory documents, validation plans and...RegulatoryTemporary workLocal area$7.82k - $10.73k
...05 Working Title: Environmental Scientist - Lead Worker Classification: SENIOR... ...success. Department Website: Director’s EEO Policy: Director’s EEO... ...environmental documents and technical studies, environmental permitting packages and regulatory permits; ensure compliance with...RegulatoryPermanent employmentFull timeLocal areaRemote workWeekend work$95k - $115k
...handbooks, policies, and internal guidelines in alignment with regulatory standards Support employee relations matters, including documentation... ...Experience in biotech, CRO, or regulated environments (GLP/GMP) is a plus Work Location & Pay Work Location: This position...RegulatoryLocal area$55 - $65 per hour
...seeking a highly motivated formulation scientist to support our clinical programs. The ideal... ...manufacturing and comply with global regulatory CMC requirements (INDs, IMPDs, NDAs). Design... ...drying. Oversee formulation screening studies in preclinical animal models....RegulatoryHourly payContract work$110k - $120k
Position: Associate Scientist Peptide Formulation Location: Newark... ...preparation for preclinical studies. The qualified candidate will... ...manufacturing and global regulatory CMC (INDs, IMPDs, NDAs) requirements... ...Works under supervision of directors to advance the development...RegulatoryContract workWorldwide$85k - $100k
...company, is seeking an experienced Associate Scientist to perform analytical testing to support... ...development, process characterization studies, and stability studies. The associate... ...and qualification protocols/reports, and regulatory filing documents per project needs.Draft...RegulatoryWork at office$188k - $266.5k
...methodology to meet project objectives, health authority guidelines, and regulatory requirements. Develops and/or applies statistical theories, methods and software. Partners in clinical development program, study design, establishing standards for clinical conduct, and the...RegulatoryContract workInterim roleLocal areaFlexible hours$248k - $352.5k
..., and software. Partners in early clinical development program study design, biomarker strategy and translational medicine strategy... ...activities and deliverables. Provides strategic statistical and regulatory guidance to anticipate challenges, mitigate risk, and ensure project...RegulatoryContract workWork at officeLocal areaFlexible hours$148.5k - $209.5k
...Assoc Scientific Regulatory Writing Director page is loaded## Assoc Scientific Regulatory Writing Directorlocations: Alameda, CAtime type: Full timeposted... ...responses, protocols, investigator brochures, clinical study reports, and other types of complex cross‑functional...RegulatoryContract workWork at officeLocal areaFlexible hours- ...governmental reimbursement for Geisinger’s hospitals, physician practices, pharmacies and specialty businesses, ensuring alignment with regulatory requirements. Job Duties Ensures the integrity, completeness, and accuracy of net patient service revenue, and third-party...RegulatoryFull timePart timeFor contractorsWork at office
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