- Merck (Rahway, NJ)
- …utilities. As we prepare to bring this asset online, we are seeking an Associate Director , Operations to lead the end-to-end operational strategy, execution, and ... meet cGMP , aseptic processing, and safety requirements. In parallel, the Associate Director , Operations will design and execute a comprehensive hiring and… more
- Merck (Rahway, NJ)
- …material handling, and the ability to integrate new technologies and cell-line platforms. The Associate Director , Process Operations Lead will be a member of ... **Job Description** The Biologics Process Research & Development organization within our Company...upstream and downstream processing. + Strong working knowledge of cGMP , Quality Systems (problem, deviations, change management, etc.), Safety… more
- Otsuka America Pharmaceutical Inc. (Trenton, NJ)
- **Job Summary** The Associate Director Controlled Substances, Quality Global Product Quality - API/DP is responsible for directing quality oversight of clinical ... stored, and transported accordance with regulatory expectations and applicable cGMP /GDP quality standards. This role has global responsibility for directing… more
- Otsuka America Pharmaceutical Inc. (Trenton, NJ)
- **Job Summary** The Associate Director , Global Product Quality - Biologics is responsible for directing quality oversight of clinical and commercial products at ... way that is in accordance with regulatory expectations and applicable cGMP /GDP quality standards. This role will direct Biologics Quality Assurance support,… more
- Bristol Myers Squibb (New Brunswick, NJ)
- …work and in their personal lives. Read more: careers.bms.com/working-with-us . The Associate Director Stability is responsible for stability product strategy and ... preparation, review and approval of stability reports and regulatory filings. The Associate Director is responsible for leading high-performance technical team,… more
- Merck (Rahway, NJ)
- …Development and Facility Engineering (EDFE) Technology Engineer position will report to the Associate Director , Engineering and will be a member of the Modality ... systems. **Responsibilities of the EDFE Technology Engineer include the following:** The Associate Director , EDFE Technology Engineer role will serve as a… more
- Merck (Rahway, NJ)
- … Principal Scientist - Device Technical and Engineering Lead ( Associate Director Equivalent)** _Our company's Device Product & Process Development (DPPD) ... position will be responsible for applying their knowledge of product and process development in the (bio)pharmaceutical and/or medical device industries to set… more
- Merck (Rahway, NJ)
- …safety, quality, and equipment decisions. This role evaluates safety, product/ process quality, and equipment performance and determines the appropriate path ... on next steps, including stop‑work when risk warrants; escalate and document per cGMP expectations. + Serve as owner and trainer for key equipment with emphasis… more
- Merck (Rahway, NJ)
- **Job Description** The Biologics Process Research & Development organization within our Company Research Labs is responsible for developing the drug substance ... material to supply clinical trials. We are also responsible for commercial process development, and development and implementation of new technologies. We work with… more
- Gilead Sciences, Inc. (Parsippany, NJ)
- …to come. Gilead Sciences PDM External Quality is currently seeking a leader at the Associate Director / Director level to lead a team of Quality Professionals ... systems and tools to the Gilead's contract organization global network. As a Director , External Quality Strategy & Operations at Gilead you will + The successful… more