- Bristol Myers Squibb (Devens, MA)
- …better place than here at BMS with our Cell Therapy team. The **Senior Manager , Quality Assurance Investigations** at the Cell Therapy Facility (CTF) in Devens, MA ... cGMP regulations and guidance. + Knowledge and proven experience in FDA , EMA, or other regulatory authority. + Demonstrated leadership, interpersonal, communication,… more
- Bristol Myers Squibb (Devens, MA)
- …personal lives. Read more: careers.bms.com/working-with-us . **Positions Summary** The Manager , Quality Assurance Disposition Support, Devens Cell Therapy role is ... in a regulated industry with 1+ year quality experience. Experience in FDA /EMA regulations in biopharmaceuticals or cell therapy manufacturing is preferred. +… more
- Bristol Myers Squibb (Devens, MA)
- …Manufacturing Practices (cGMPs). In the capacity of QA Shop Floor Support, the ** Manager , Shop Floor QA, Cell Therapy** shall be responsible for handling Quality ... as Manufacturing Execution systems (MES), Enterprise Resource Planning (ERP) **Basic Requirements :** + Bachelor's degree in STEM field preferred. High school… more
- Abbott (Phoenix, AZ)
- …growth expectations + Complies with US Food and Drug Administration ( FDA ) regulations, other regulatory requirements , company policies, operating procedures, ... Disease (ID) is seeking a highly motivated, technically proficient **Key Account Manager ** with strong business acumen and selling skills to oversee and grow… more
- Regeneron Pharmaceuticals (Warren, NJ)
- The Senior Manager , Hematology, Clinical Scientist leads in the development, evaluation, planning and execution of clinical studies and ensures integrity and ... study data of a clinical development program. The Sr. Manager leads in a matrix environment as part of...perform quality review + Maintains compliance in accordance with FDA , EMEA, ICH and GCP guidelines as well as… more
- WuXi AppTec (Middletown, DE)
- …startup-like environment while ensuring strict adherence to GMP and regulatory requirements . Candidates must have deep knowledge of regulatory guidelines to guide ... oral dosage, API, and aseptic small molecule production to ensure compliance with FDA , EMA, and other regulatory bodies. + Review and approve facility, utility and… more
- Novo Nordisk (Plainsboro, NJ)
- …provider interactions and developing and implementing regulatory strategies with the FDA to providing medical education and collecting data to support efficacy ... up-to-date knowledge of the Regulations and Guidelines issued by the FDA along with other industry periodicals impacting pharmaceutical product quality issues… more
- Conagra Brands (Omaha, NE)
- …+ Minimum of 5 years of food industry regulatory experience. + Knowledge of FDA and USDA regulations and requirements + Knowledge and demonstrated ability to ... ConAgra Foods businesses. + Maintains in depth state-of-the-art knowledge of FDA , USDA, and state-level regulations. + Provides leading support for traceability… more
- The Clorox Company (Alpharetta, GA)
- …+ Regulatory Team to identify and manage non-tariff barriers such as EPA and FDA requirements for imports/exports. + Other GTC Regional Leaders for cross-border ... & Anti-boycott; Identifying and managing non-tariff barriers ( _e.g.,_ EPA, FDA import/export regulatory matters); Import/export laws and regulations in countries… more
- Insight Global (Beachwood, OH)
- …analysis plans and protocol review cycles. o Submit and manage regulatory applications ( FDA and other global agencies). - Clinical Execution & Oversight o Oversee ... review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/. Skills and Requirements Required Qualifications . Minimum 3-5 years of experience… more