- Aequor (Cincinnati, OH)
- Quality Control Analyst I Does the position allow for the worker to be virtual/remote? No Temp to Perm: Temp to perm based on openings and performance Shift ... Monitoring chemical and dry stock inventory Assist with ordering chemicals/materials COMPLIANCE AND QUALITY Basic knowledge and understanding of USP, cGMP, and… more
- Abbott (Columbus, OH)
- …114,000 colleagues serve people in more than 160 countries. **Senior Customs Compliance Analyst ** **Working at Abbott** Our nutrition business develops ... role is to provide technical and analytical support for customs and trade compliance matters at the site/division level, ensuring compliance with all relevant… more
- Abbott (Irving, TX)
- …location in **Irving, TX** currently has an opportunity for a **Customs and Trade Compliance Analyst ** . This new team member will provide technical and ... analytical support for customs and trade compliance matters at the site/division level, ensuring ...relevant customs regulations and trade laws including, 19CFR, 15CFR, FDA , USDA, other PGAs and data metrics. **Responsibilities** +… more
- AbbVie (North Chicago, IL)
- …across a wide group of multi-functional partners and OEC teams, the Senior Analyst , Compliance Analytics, supports the execution and adoption of our ... Compliance Analytics Platform, including Office of Ethics and ...and authority of government agencies and industry partners, PhRMA, FDA , OIG, PDMA, Affordable Care Act, PDMA, ACCME, etc.)… more
- Olympus Corporation of the Americas (Center Valley, PA)
- …(For example: death, serious injury, legal papers, and literature reviews). The Analyst III requires a thorough understanding of FDA regulatory requirements ... clinical assessments as requested. The ability to maintain quality documents to ensure compliance with FDA regulations and guidance documents relating to these… more
- Catalent Pharma Solutions (Harmans, MD)
- Job Description **Commercial Operations Analyst ** Catalent Pharma Solutions is looking to hire a **Commercial Operations Analyst ** to support our growing team in ... vaccines & hard-to-express recombinant proteins and oncolytic viruses. Our FDA -licensed, state-of-the-art CGMP manufacturing facility for Gene Therapies is located… more
- Sanofi Group (Morristown, NJ)
- **Job Title:** Business Analyst Manager, SSDM **Location: Morristown, NJ** **About the Job** Are you ready to shape the future of medicine? The race is on to speed ... Your skills could be critical in helping our teams accelerate progress. Business Analyst Manager role encompasses many of the operational aspects within the System… more
- Glenmark Pharmaceuticals Inc., USA (Monroe, NC)
- Senior Quality Control Analyst Department: Chemistry Location: Monroe, NC START YOUR APPLICATION ... for this position will be: perform QC analysis in compliance to cGMP in line with standards prescribed by...to align with corporate guidelines. + Comply with applicable FDA and international regulatory laws/standards and the Code of… more
- Caris Life Sciences (Phoenix, AZ)
- … Analyst -Equipment position is responsible for assisting in company-wide compliance to all applicable regulatory requirements and assisting with the day-to-day ... equipment calibration and maintenance program. **Job Responsibilities** + Maintain compliance to all applicable regulatory requirements (CLIA, NYS, CAP, ISO,… more
- Curia (Albany, NY)
- Manufacturing Quality Assurance Analyst I, Albuquerque, NM Night Shift Build your future at Curia, where our work has the power to save lives! Curia is a global ... + Learning platform + And more! Summary: The Manufacturing Quality Assurance (MQA) Analyst I role is an entry-level, developmental position. The MQA Analyst … more
- University of Washington (Seattle, WA)
- …and reputational risks by ensuring strict compliance with the CMS and the FDA regulations and guidelines. The Senior Analyst is a key position in maintaining ... clinical researchers bringing important new therapies to our patients in compliance with evolving regulatory requirements. **The Clinical Trials Office, in… more
- Vitalief (New Brunswick, NJ)
- …whether each trial is a qualifying trial per CMS regulations, and assesses compliance with other regulatory requirements, including FDA and NIH guidelines. + ... We are seeking a talented and enthusiastic Senior Clinical Research Financial Analyst to join our exceptional team (as full-time, fully benefited Vitalief employee)… more
- Takeda Pharmaceuticals (Los Angeles, CA)
- …true to the best of my knowledge. **Job Description** **Senior Quality Analyst - Nights** **Takeda Pharmaceuticals** **About the Role:** You will perform all primary ... activities for Teardown, Fractionation, and Purification following cGMP, GDDP, FDA and Regulatory Standards, ISO requirements, and internal standard operating… more
- Xcelerate Solutions (Frederick, MD)
- Program Analyst IV - Medical Regulatory & Acquisition Strategy Xcelerate Solutions is seeking a Senior program analyst who will support Joint Program Executive ... knowledge points and risks through the medical portfolio + Track and trend FDA regulatory intelligence + Assist with full lifecycle project management and oversight… more
- Universal Technical Resource Services, Inc. (Marlton, NJ)
- …budget. This position, Fighter Military Flight Operations Quality Assurance (MFOQA) Flight Data Analyst ( FDA ), works with the Air Combat Command (ACC) MFOQA ... Services, Inc. (UTRS) is currently seeking a Fighter MFOQA Analyst to join our team! At UTRS, we enjoy...Fighter MFOQA fleet (F-16, F15 variants). Additionally, the Fighter FDA enhances flight safety through the management and analysis… more
- BioFire Diagnostics, LLC. (Durham, NC)
- …working a 2-2-3 rotation schedule. This position is in a fast-paced, FDA regulated environment in the Medical Devices/Diagnostics Industry. The QC Biochemistry ... Analyst 2 will be in a key position in...accurate, thorough, and timely manner. Documents test results in compliance with procedures and GDP requirements. + Ensures review… more
- Teva Pharmaceuticals (West Chester, PA)
- IT Business Process Analyst III Date: Jul 9, 2025 Location: West Chester, United States, Pennsylvania, 19380 Company: Teva Pharmaceuticals Job Id: 62740 **Who we ... opportunity** We are currently recruiting an IT Business Process Analyst to support the local R&D laboratory computerised systems...that system implementations are in keeping with the relevant FDA 21 CFR Part 11, GxP guidelines as well… more
- Kelly Services (Lodi, CA)
- …supporting the Bulk Buffer, Reagents, and Bead Production Laboratories. The Laboratory Analyst is responsible for performing tasks in compliance with Good ... **Laboratory Analyst ** **Kelly(R) Science & Clinical is seeking a...experience Knowledge & Skills: + Familiarity with cGMP, cGLP, FDA , and ISO standards + Ability to follow SOPs,… more
- Insight Global (Jacksonville, FL)
- …defined by structured SDLC and STLC processes that leverage templated forms to ensure FDA and ISO Regulatory compliance . We are a company committed to creating ... Job Description The IT Business Analyst -- I (Junior) is a pivotal part...support of business systems and applications. As a Business Analyst (I), you will participate in requirements gathering sessions… more
- Glenmark Pharmaceuticals Inc., USA (Monroe, NC)
- …performing and overseeing complex microbiological testing and environmental monitoring (EM) in compliance with cGMP, USP, FDA , and internal quality standards. ... Senior Microbiology Analyst Department: Microbiology Location: Monroe, NC START YOUR...This position is in a fast-paced, FDA regulated environment in the Pharmaceutical Industry. This role… more
