- Legend Biotech USA, Inc. (Raritan, NJ)
- …in the treatment of multiple myeloma. Legend Biotech is seeking an Associate Director for Operations Compliance and Investigations Managementas part of the ... Company Information Legend Biotech is a global biotechnology company dedicated to treating, and one...team based in Raritan, NJ. Role Overview The Associate Director for Operations Compliance and Investigations Management… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …effective communications within the GPT, by interacting with other GxP QA functions ( GMP / IMP QA, Audit Compliance , Quality Management System [QMS] QA, PV/MA ... people. Under the Group's 2025 Vision to become a " Global Pharma Innovator with Competitive Advantage in Oncology," Daiichi...to ensure appropriate management review of all quality and compliance related topics including the review of Key Quality… more
- Merck & Co. (Rahway, NJ)
- …of continuous learning and improvement, scientific and operational excellence, safety, GMP and compliance mindset, and collaboration with various partners ... Job DescriptionOur company is a global healthcare leader with a diversified portfolio of...from the bench top to the Good Manufacturing Practice ( GMP ) manufacturing facilities, our Scientists use cutting-edge science to… more
- Catalent (Harman, WV)
- Position Summary The Director , Quality Systems is responsible for the management and oversight of the core quality systems, including investigation/deviation ... department investigation writers. Administers the CAPA Tracking System for general GMP use and internal audits while tracking completion of commitmentsPerform… more
- Merck & Co. (North Wales, PA)
- …Systems for seamless integration and realize synergies where available while ensuring compliance to GMP requirements.- Ensure alignment to corporate policies as ... Division QMS team for QMS updates as needed.Support establishment of New Modalities Global Quality Management processes and Regulatory Compliance plan in support… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionFLEx is a set of multi-modality Drug Product development and GMP clinical manufacturing assets being constructed in the Rahway, New Jersey site, to ... across two co-leader roles, and includes operations that support end-to-end GMP clinical supply manufacture and product/process development, as well as oversight… more
- Merck & Co. (Millsboro, DE)
- Job DescriptionAssociate Director , Animal ServicesAbout the JobAnimal Health in Millsboro Delaware seeks to add an Attending Veterinarian in the role of Associate ... Director .This position will have overall responsibility for oversight and...company's Millsboro Animal Health facilities. This role is highly compliance -driven in accordance with State and Federal regulations as… more
- Insmed Incorporated (Bridgewater, NJ)
- …in New York™, and Best Workplaces for Millennials™ lists.OverviewReporting to the Executive Director Quality GMP Compliance , the Director , Quality ... Company DescriptionInsmed is a global biopharmaceutical company on a mission to transform...suppliers. Using influence, active engagement, and an understanding of compliance requirements, work with critical suppliers to ensure quality,… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …medicines to help people. Under the Group's 2025 Vision to become a " Global Pharma Innovator with Competitive Advantage in Oncology," Daiichi Sankyo is primarily ... areas centered around rare diseases and immune disorders.Summary The Associate Director , RACMC Portfolio Products, will be responsible for regulatory CMC (Chemistry,… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- … compliance with SDEA requirements. Relationships This position reports to the Director , Case Review & Compliance Reporting within Patient Safety. This ... to the following: all units in Patient Safety, NNI GXP Support, NNI Legal, NNI Compliance , NNI Commercial, NNI Finance, Global Business Services (GBS), PV & GDP… more
- Merck & Co. (Rahway, NJ)
- … compliance investigation, change management and the authoring of GMP documentation in any of our enabling facilities.Additional Supported AreasAs required ... compliance investigations and change management.Familiarity with US and EU GMP and Safety compliance regulationsEffective interpersonal and communication… more
- Merck & Co. (Durham, NC)
- …Periodically reviews automation documents, preventive maintenance, and SOPs to ensure compliance with GMP and safety.Assisting in the development and ... implementations of process change control, Delta V Network and troubleshooting in compliance with system life cycle (SLC), GMP , Data integrity, safety,… more
- Merck & Co. (Rahway, NJ)
- …responsibility. The Specialist - Manufacturing Automation position will report to the Director , Engineering, Automation Lead position and will be a member of the ... systems and equipment utility metering systems.-This role will collaborate with Global Workplace Enterprise Solutions (GWES) in prioritizing a portfolio of… more
- Merck & Co. (Durham, NC)
- …and Local code requirements for quality, good manufacturing practices ( GMP ), equal employment opportunity, finances, labor, employee, environment and safetyTactical ... and business plan; receives guidance and oversight from Operations Associate Director and Director ;Interprets client and/or customer needs and assesses… more
- Merck & Co. (Durham, NC)
- …safest and most compliant operation around the network.EMSS has an Associate Director opening for the Teknika maintenance and Engineering team. The selected ... with optimized product quality and manufacturing processes and regulatory compliance . GENERAL PROFILE Provides leadership and direction through individual… more
- Merck & Co. (Rahway, NJ)
- …to ensure optimal automation in pharmaceutical manufacturing.Understand and adhere to CFR, GMP , and data integrity regulations to ensure compliance with ... Automation Specialist - Engineering Auto Eng position will report to the Director , Engineering, Automation Lead position and will be a member of the… more
- Catalent (Manassas, VA)
- …their team to achieve objectives and results. Work closely with the Director Procurement, the Global Procurement Organization (GPO), Site Operations, Business ... Site Procurement ManagerPosition Summary Catalent is a global , high-growth, public company, and a leading partner...a Patient First culture through excellence in quality and compliance , and to the safety of every patient, consumer… more
- Sumitomo Pharma (Columbus, OH)
- …clinical trials and/or commercial phases. The Associate Director ensures compliance with GMPs, SMPA procedures and applicable global Regulatory guidelines ... **Associate Director , GMP Quality Control** Sumitomo Pharma... of GMP Quality Control, who oversees GMP compliance of manufacturing, testing and release… more
- Teva Pharmaceuticals (Parsippany, NJ)
- …making a difference, and new people to make a difference with. **The opportunity** The Director of Global Quality Systems Compliance plays a critical role in ... across Teva Global Operation (TGO) to advance compliance , efficiency, and customer experience. The Director ...years of experience in Quality or Operations in a GMP environment. Understanding and insight into different aspects of… more
- Gilead Sciences, Inc. (Foster City, CA)
- …report to Executive Director , Supplier Quality Management and Audits, within the Global Quality Systems & Compliance department. The role is highly visible, ... seeking an industry leader for a Director , Quality Assurance role, who will...program and Qualification Process by leading initiatives to maintain compliance to global regulations and standards +… more
