- Otsuka America Pharmaceutical Inc. (Washington, DC)
- 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. (Washington, DC)
- **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. (Washington, DC)
- **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. (Washington, DC)
- 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
- The US Pharmacopeial Convention (USP) (Rockville, MD)
- …mindset. + Experience with regulatory, clinical development, quality assurance, GMP in biopharmaceutical market environment. + Existing global network with ... inclusive and collaborative work environment. **Brief Job Overview** The Director , Global Business Development, Biologics is a...standards, you will play a vital role in increasing global access to high- quality medicines through public… more
- Amgen (Washington, DC)
- …Amgen team. Join us and transform the lives of patients while transforming your career. ** Director of Global Product Safety** **What you will do** Let's do this. ... reporting to the Vice President and Chief Security Officer, Global Security (GS) this vital role in the GS...but not required. + Solid working knowledge of GxP ( GMP , GDP, etc.) environments is necessary. + At least… more
- Jabil (Hunt Valley, MD)
- …industries and a vast network of over 100 sites worldwide, Jabil combines global reach with local expertise to deliver both scalable and customized solutions. Our ... Job Description Job Overview: In this role the Senior Director , Facilities & Engineering will be responsible for the...all aspects of engineering with a special focus on GMP Manufacturing equipment uptime, including the routine reporting of… more
- The US Pharmacopeial Convention (USP) (Rockville, MD)
- …you contribute to USP's public health mission to expand equitable access to high- quality , safe medicines and to improve global health through public standards ... collaborates with leading authorities in health and science to develop quality standards for medicines, dietary supplements, and food ingredients. USP's fundamental… more
- ThermoFisher Scientific (Washington, DC)
- …of compliance processes and systems in a manner consistent with global quality systems requirements, corporate standards, current regulatory requirements ... Director , Compliance will report to the Head of Global Compliance. The incumbent will work to ensure the...the business. Deliver safe & effective products and make Quality a competitive advantage by achieving outstanding GMP… more
- Sumitomo Pharma (Washington, DC)
- …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
- Gilead Sciences, Inc. (Washington, DC)
- …& Influence** Cultivate strong, collaborative relationships across Gilead's global functions, including Quality , Manufacturing, Technical Development, ... **Job Description** . **Strategic Leadership & Vision** Define and drive global regulatory strategies for combination products, ensuring alignment with corporate… more
- The US Pharmacopeial Convention (USP) (Rockville, MD)
- …and public health standards, you will play a vital role in increasing global access to high- quality medicines through public standards and related programs. ... is driven by a commitment to fairness, integrity, and global collaboration. This belief is embedded in our core...sales) experience a plus. + Experience with regulatory compliance, quality control, quality assurance or GMP… more