- Takeda Pharmaceuticals (Boston, MA)
- …and Statistics, with at least 3 years of experience in GCP Quality/ Compliance . + Advanced knowledge of pharmaceutical development, medical affairs and ... mechanism to monitor the health of the QMS including the identification of systematic quality compliance risks and implementation of robust mitigation… 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, ... of the US clinical landscape and market dynamics of relevance to the respective TA. The Director...Systems and Payers strongly preferred. + Demonstrated experience with pharmaceutical drug development and the use of … more
- AbbVie (North Chicago, IL)
- …equivalent) is required; advanced degree preferred + 10+ years of pharmaceutical , healthcare, or clinical research related experience; Compliance or Quality ... of Clinical Operation functions + Oversees the establishment, maintenance, and monitoring of compliance metrics in support of Senior Leader Review and the… more
- Curia (Albuquerque, NM)
- …your future at Curia, where our work has the power to save lives. The Director of Environmental, Health & Safety (EH&S) is a senior leadership role accountable ... for shaping and driving the strategic vision of EH&S programs across the pharmaceutical manufacturing...of robust, site-wide EH&S systems that ensure full compliance with all applicable federal, state, and local regulations… more
- Bausch Health (Bridgewater, NJ)
- …itwhere your skills and values drive our collective progress and impact. 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
- Bausch Health (Bridgewater, NJ)
- …+ Bachelors 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
- Lilly (Indianapolis, IN)
- …in the resolution of issues with suppliers with the shared goal of ensuring Lilly's global pharmaceutical supply chain operates effectively and efficiently ... ensuring standard approaches across the networks.Support periodic management reviews of supplier performance. + Regulatory Compliance : Stay...following experience: + Minimum of 7 years of experience in the pharmaceutical or other… more
- Takeda Pharmaceuticals (Boston, MA)
- …present, and discuss complex medical and scientific data + Understanding of pharmaceutical clinical development and product life-cycle management, clinical ... of scientific communications strategy and deliverables, the **Associate Director , Scientific Communications Lead, Hematology** proactively defines and drives the… more
- Otsuka America Pharmaceutical Inc. (Princeton, NJ)
- **Job Summary** We are seeking an experienced and dynamic Executive Director of R&D Global Quality to join our team. This pivotal role will be responsible for ... program are effective and efficient in identifying, detecting, and correcting non- compliance and mitigating risks, The performance of the Quality Systems… more
- Catalent Pharma Solutions (San Diego, CA)
- …related sciences and minimum 11 to 13 years relevant industry experience + BS in Pharmaceutical related sciences and minimum of 15 years of relevant industry ... **Title: Director Product Development** **About Catalent San Diego:** Catalent,...delivery technologies, and multi-modality manufacturing, Catalent supports the acceleration of development programs and the launch of … more