- Merck (Rahway, NJ)
- …The other team drives program governance and privacy operations, supporting privacy compliance through the development and maintenance of program strategy, ... and highly regulated digital landscape, and foster a culture of responsible data stewardship across the organization. The Deputy...a large, global corporation or law firm. Legal or compliance experience in the pharmaceutical or life… more
- Bristol Myers Squibb (Summit, NJ)
- …systems validation requirements and good documentation practices. + Advanced knowledge of pharmaceutical , manufacturing and laboratory systems and equipment. + ... The individual supports multiple projects and ongoing work activities of low to moderate complexity to ensure compliance...analyze meaningful metrics. **Knowledge & Skills:** + Thorough knowledge of cGMP in the pharmaceutical industry. +… more
- BeOne Medicines (Nashville, TN)
- …a minimum of 8 years' clinical experience and/or success within other biotech/ pharmaceutical companies For Director Level: MD, PharmD., PhD, or DO, within a ... Liaison** role and an individual contributor role. The **Senior Field Medical Director (SFMD)** will support BeOne Pre-Clinical and Clinical pipeline development by… more
- IQVIA (Washington, DC)
- …program objectives. + Develop and implement policies and procedures that maintain high levels of compliance and quality care. + Analyze program data and metrics ... The Associate Director serves as the key point of...skills to drive program improvements. + Familiarity with healthcare compliance requirements and pharmaceutical field operations. **Role… more
- Gilead Sciences, Inc. (Santa Monica, CA)
- …8+ years of quality and enterprise risk management within the pharmaceutical or biopharmaceutical industry OR + Master's degree in a scientific discipline (eg, ... 10+ years of quality and enterprise risk management within the pharmaceutical or biopharmaceutical industry OR + Bachelor's degree in a scientific discipline… more
- Fujifilm (College Station, TX)
- …orviral products according to cGMPs in a timely manner. + Ensuring the full compliance to OSHA and cGMP regulations of the manufacturing operations at all ... products in single rooms. + Maintain the operational facility in the highest level of cGMP compliance per FDA and customer expectations. + Build, maintain and… more
- Bausch Health (Bridgewater, NJ)
- …+ Bachelor's degree in science or health related field + Knowledge of pharmaceutical brand industry regulatory affairs discipline throughout the product/dossier ... Director , Regulatory Affairs handles regulatory development and post-approval/regulatory compliance for assigned products. Participates on the product development/life-cycle… more
- Bausch Health (Bridgewater, NJ)
- …skills and values drive our collective progress and impact. Job Scope: The Director of Regulatory Affairs coordinates and oversees regulatory development and ... years relevant pharmaceutical industry and regulatory experience + Knowledge of pharmaceutical brand industry regulatory affairs discipline throughout the… more
- Boehringer Ingelheim (Ridgefield, CT)
- …and medical market insights into medical tactical plans for effective launches of pharmaceutical products in the US, integrated evidence generation plans, ... relevant internal stakeholders with emphasis on leading the medical affairs aspects of these plans. **Requirements** **SR Associate Director Education &… more
- Gilead Sciences, Inc. (Santa Monica, CA)
- …gene therapy product manufacturing. This role ensures the safety, quality, and compliance of our products and processes through the development, implementation, ... create more tomorrows. **Job Description** We are seeking a Director for Sterility Assurance role. This is a critical...of experience in a microbiology/virology role within the pharmaceutical or biotechnology industry, with a focus on sterile… more