- Merck (Rahway, NJ)
- …in pharmaceutical or combination product research, development and/or manufacturing + Experience with CMC regulatory where drug is the primary mode of action ... Associate Principal Scientist position is equivalent to an Associate Director position. Under direction from a Director ,...control activities and documentation reviews + Provide evaluations of regulatory state of affairs of any devices… more
- Bausch Health (Bridgewater, NJ)
- …it-where your skills and values drive our collective progress and impact. The Associate Director , Regulatory Affairs handles regulatory development and ... assigned pharmaceutical products. + Coordinate/Liaise with BHC country-specific pharmaceutical Regulatory Affairs personnel for international submissions and… more
- J&J Family of Companies (Raritan, NJ)
- …regulatory strategies are in alignment with product portfolio, regional strategies, CMC - Regulatory Affairs strategy, commercial and market access ... health for humanity. Learn more at https://www.jnj.com **Job Function:** Regulatory Affairs Group **Job Sub** **Function:** ...**We are searching for the best talent for a Director , North America Regulatory Leader (Oncology) to… more
- Bayer (Whippany, NJ)
- …Files, etc.); + Lead and/or participate in key new product development Regulatory Affairs Teams and/or Global Project Teams; effectively collaborate with ... **Email:** hrop_###@bayer.com **Job Segment:** Medical Device, Biomedical Engineering, Compliance, Regulatory Affairs , Product Development, Healthcare, Engineering, Legal,… more
- Teva Pharmaceuticals (Parsippany, NJ)
- …independently, as needed + Partners cross-functionally with departments such as Regulatory Affairs , Toxicology, CMC /Formulations, Biostatistics, Legal, ... documents (ie protocols, Investigator's Brochures, clinical study reports, summaries for regulatory submissions). The Director , Clinical Development will provide… more
- Organon & Co. (Jersey City, NJ)
- …colleagues in preclinical science, data science, clinical operations, regulatory affairs , chemistry, manufacturing and control ( CMC ), project management and ... in the US + There are **2 openings** The Director , Clinical Pharmacology Lead will be responsible for contributing...are sound, based on the most up-to-date literature and regulatory guidance and support the approved early development plans.… more
- Bausch Health (Newark, NJ)
- …Project Management, CMC , Analytical Sciences, Nonclinical, Clinical Operations, Clinical/Medical Affairs , Biostatistics, and Regulatory Affairs . + Lead ... it-where your skills and values drive our collective progress and impact. The Director of Clinical Pharmacology will provide expertise and support to internal and… more