- Otsuka America Pharmaceutical Inc. (Trenton, NJ)
- The Director , Global Product Quality , GMP Processes is a strategic leadership role responsible for **benchmarking, standardizing, and optimizing ... continuous improvement** across all regions and product lines. The Director will lead global initiatives to harmonize...operational efficiency. + GMP Compliance: Ensure all quality processes meet global regulatory requirements (eg,… more
- Otsuka America Pharmaceutical Inc. (Trenton, NJ)
- **Job Summary** The Associate Director , Global Product Quality - GMP Process is responsible for enabling the optimization and harmonization of key GMP ... and subject matter expertise to global teams on GMP compliance and quality system execution. **Qualifications** Required + Bachelor's degree in Pharmacy,… 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 ... product integrity while optimizing operational efficiency. + Works collaboratively within the Global Quality Dept. and other functions within OAPI and OPDC… more
- Otsuka America Pharmaceutical Inc. (Trenton, NJ)
- The Associate Director of Global Supplier Quality will be responsible for the execution of supplier quality audit and monitoring across the company's ... + **Compliance & Documentation** + Ensure supplier compliance with global regulatory requirements (eg, FDA, EMA, ICH). + Prepare..., with 2+ years in supplier or external manufacturing quality . + Strong knowledge of GMP regulations… more
- Merck (Rahway, NJ)
- **Job Description** The Director , Technical Operations within Global Clinical Supply (GCS) is responsible for technical leadership in support of GCS global ... equipment-based challenges when required. The technical lead may also manage global infrastructure projects to establish, upgrade, and improve the GCS packaging,… more
- Teva Pharmaceuticals (Parsippany, NJ)
- Senior Director , Site Quality Head, Goa Date: Dec 1, 2025 Location: Parsippany, United States, New Jersey, 07054 Company: Teva Pharmaceuticals Job Id: 63901 ... development, standardization, implementation, monitor effectiveness and continuous improvement of Quality Systems, global and local compliance programs, industry… more
- Taiho Oncology (Princeton, NJ)
- …MAA's, INDs, CTAs, DMFs, ASMFs, etc. and ensures that they conform to current GMP and meet global regulatory requirements. The incumbent may participate in ... Directs and coordinate regulatory activities of external consultants in consultation with Global Executive Director or designee. + Prepare project and/or status… more
- Honeywell (Hamilton, NJ)
- …and quality . Operating within a matrixed organization, the Sr Director will collaborate across functions and geographies to deliver customer-centric solutions ... The **Sr Director of Software Sales - Life Sciences** will...process development to commercial scale-up + Demonstrated knowledge of quality systems and regulatory frameworks (eg, GMP ,… more
- Merck (Rahway, NJ)
- …execution, along with leadership skills to shape the technical capabilities lead a global , cross-modality technical team. The Associate Director will lead a team ... **Job Description** Reporting into the Director , Logistics and Distribution Technology the Associate Director , Logistics and Distribution Technology will be… more
- Sumitomo Pharma (Trenton, NJ)
- …Director , Commercial Manufacturing Validation** . This role functions within SMPA's Global Technology and Quality organization. In this capacity, the ... Sumitomo Pharma Co., Ltd., is a global pharmaceutical company based in Japan with operations...are implemented and updated for all development and commercial GMP programs. The individual must have the ability to… more
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