Senior Biocompatibility Scientist II — Regulatory & Risk Expert
Abbott Laboratories
Abbott Laboratories in Santa Clara, CA seeks a Senior Biocompatibility Scientist II to support biocompatibility evaluations across product lifecycle. You will develop evaluation plans, review data, and collaborate with cross-functional teams to ensure compliance with ISO 10993, FDA guidance, and EU regulations. The role emphasizes independent technical leadership within a matrixed environment, with responsibilities spanning design changes, regulatory submissions, and risk assessment. #J-18808-Ljbffr Abbott Laboratories
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- Conduct retrospective biocompatibility gap assessments across legacy product... ...(BERs), toxicological risk assessments (TRAs), and material... ...subject matter expert during FDA/notified body interactions... ...interactions, audits, and responses to regulatory questions or deficiency...SeniorRiskRegulatoryContract work
$120k - $145k
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...environmentalist/trainee or support staff. Working ability to identify regulatory infractions and recommend corrective actions. Typical Working... ...making at the state and local levels such as the Behavioral Risk Factor Surveillance System, Immunization Registry and Office of...RiskRegulatoryHourly payPermanent employmentFull timeTraineeshipWork at officeLocal area$76k - $125.3k
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...beyond at Job Title: Sr. FSQR Scientist - Compliance & Labeling... ...deeply knowledgeable team of regulatory compliance and legal pros, each... ...government affairs, policy, risk management, regulatory compliance... ...building relationships with senior leaders and the business partners...SeniorRiskRegulatoryTemporary workWork experience placementWork at officeFlexible hoursShift work$130k - $210k
...Preclinical Principal Scientist will serve as a key... ...contributor, subject matter expert (SME), and Project... ..., and Preclinical Regulatory Strategy. This will include... ...) to execute both Biocompatibility / Safety and Efficacy... ...and safety risks. Maintain current...RiskRegulatoryContract workTemporary workApprenticeshipLocal areaWork from home- Sr. Scientist, Downstream Process Development United States About GenScript Founded in 200... ...support process technology transfer, cGMP risk evaluation, and deviation management.... ...in the preparation of CMC sections for regulatory submissions (IND, Annual Reports, and BLA...SeniorRiskRegulatoryTemporary workFlexible hours
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Senior$86.32k - $129.48k
...only one choice. R&D Sterile Disposables Senior Engineer (Microbiology & Biocompatibility) - Indianola, PA R&D Sterile Disposables... ...Experience supporting FDA and/or other regulatory body submissions, testing strategies, or Class II medical device product registrations; Practical...SeniorRegulatory- Tonix Pharmaceuticals in Frederick, MD is seeking a Scientist II to support preclinical programs through in vitro and nonclinical assays... ...high-quality data, and document results to support program decisions and regulatory activities. #J-18808-Ljbffr Tonix Pharma LimitedRegulatory
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