- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Responsible to complete on paper basis audit and to monitor vendor performance management program. Support the issue and communication of audit plans, agenda and ... program to ensure adequate qualification of auditors per regulatory expectations.Risk Management and Vendor Performance: Responsible to ensure the risk management… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …as other research areas centered around rare diseases and immune disorders. SummaryThe Associate Director will provide program management support across all ... and stakeholders in Daiichi Sankyo to manage the creation of the product specific Medical Strategy and Objectives. Collaborates with all Medical Affairs functional… more
- Merck & Co. (Rahway, NJ)
- …Capital Projects, Chemical Engineering, Clinical Development, Communication, Communication Management , Customer-Focused, Data-Driven Decision Making, Drug Product ... Troubleshooting, Pharmaceutical Process Development, Process Control Automation, Process Optimization, Product Formulation, Project Management , Quality Control … more
- Merck & Co. (Rahway, NJ)
- …Medical Affairs, Ophthalmology, Patient Assistance Programs, People Leadership, Pricing Processes, Product Development, Product Management {+ 5 ... and maximizing the value of its Ophthalmology portfolio. Reporting to the Associate Vice President, Global Market Access, Global Pharma, the Executive Director… more
- Organon & Co. (Jersey City, NJ)
- **Job Description** **The Position** The Associate Director , Biopharmaceutics will provide expert biopharmaceutical guidance on the pharmacokinetic performance ... for the general medicines portfolio of products marketed worldwide. The Associate Director , Biopharmaceutics will also be responsible for contributing… more
- Organon & Co. (Jersey City, NJ)
- **Job Description** **The Position** We are looking for an experienced Associate Director , Program Manager to join our team. This successful candidate will ... provide program management expertise as an individual contributor to teams leading...overall program strategy and objectives for achieving the target product profile and value proposition. + Lead the establishment… more
- GRAIL (Trenton, NJ)
- …Lab Operations, and other stakeholders to support regulatory strategy development, product validation, audits, promotional material review, on-market product ... and provide direction to regulatory staff and, when required, participate in senior management meetings as a delegate. The role fosters a work culture aligned with… more
- Organon & Co. (Jersey City, NJ)
- **Job Description** **The Position** Reporting to the Director or Executive Director in Organon Regulatory Chemistry, Manufacturing and Controls (CMC), the ... Associate Principal Scientist is responsible for developing and implementing...not limited to: **Responsibilities** + Serve as the CMC Product Lead for assigned products and be accountable for… more
- Parexel (Trenton, NJ)
- …**Collaboration** + Reports to Director of Clinical Site Operations (DCSO) or Director of Site Management and Monitoring (DSMM) + Partners with SCP and ... **Job Purpose:** The Senior Clinical Research Associate I (Sr. CRA) is responsible for the... I (Sr. CRA) is responsible for the site management , site monitoring and close-out of assigned clinical trials… more
- Organon & Co. (Jersey City, NJ)
- **Job Description** **The Position?** Reporting to the Director in Organon Regulatory CMC,?the Associate Principal Scientist is responsible for?developing ... in accordance with global regulations and?guidance, and?Organon procedures.? The Associate Principal Scientist will lead the?preparation and submission of CMC… more
