• Novo Nordisk Inc. (Plainsboro, NJ)
    …enable compliance with Deviation process requirements across NNI and global as applicable Develops and executes regular surveillance, follow-up, and reporting ... of the value chain and customer focus. This role enables and ensures compliance against health authority regulations and Novo Nordisk requirements in relation to… more
    HireLifeScience (07/30/25)
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  • Novo Nordisk Inc. (Plainsboro, NJ)
    …to enable compliance with QMS process requirements across NNI and global as applicable Proactively identifies risks/quality drift in external vendor and NNI ... of the value chain and customer focus. This role enables and ensures compliance against health authority regulations and Novo Nordisk requirements in relation to… more
    HireLifeScience (07/30/25)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …other research areas centered around rare diseases and immune disorders. SummaryThe Manager Audits & Compliance , GCP/Document Audits supports end-to-end audit ... 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… more
    HireLifeScience (06/20/25)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …Regulatory Process Manager will be a key member of the Global Regulatory Affairs (GRA) Process Excellence & Analytics function, responsible for ensuring Daiichi ... for cardiovascular diseases, under the Group's 2025 Vision to become a " Global Pharma Innovator with Competitive Advantage in Oncology," Daiichi Sankyo is primarily… more
    HireLifeScience (05/08/25)
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  • Merck & Co. (Rahway, NJ)
    …will require routine interaction with Partner Groups such as GES ( Global Engineering Services), Facilities Management (FM/GWES) and Original Equipment Manufacturers ... (QN) reporting, investigations, and any related corrective action/preventive action ( CAPA ).- Facilitate equipment/system changes, execute periodic reviews and support… more
    HireLifeScience (07/26/25)
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  • Gossamer Bio (San Diego, CA)
    …investigations and CAPA activities related to logistics operations. Ensure compliance with Gossamer policies, safety standards, and global regulations. ... includes inventory management, shipping and receiving, vendor management, and import/export compliance . A strong understanding of global trade regulations, GMP… more
    Upward (07/11/25)
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  • elf Beauty (New York, NY)
    …to Active Pharmaceutical Ingredients (API). Travel as needed. Partner with the QMS Manager to develop a global QMS, maintain, and fine-tune with matching ... Manufacturers, Suppliers, local Authorities) Responsibilities: Ensures the ongoing quality and compliance of marketed products Responsible for the management of post… more
    Upward (07/27/25)
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  • LanceSoft (Pittsburgh, PA)
    …: 675 Kendall St 02147 Cambridge MA (Hybrid: 2x per week) Job Title: Senior Manager , Global Pharmacovigilance (PV) Quality Assurance Pay Rate : $ 105.00 to $ ... a strong partner with Expertise Areas (EAs) in the enhancement of the global pharmacovigilance system, including ensuring compliance with GVP regulations. This… more
    Upward (07/29/25)
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  • Lonza (Portsmouth, NH)
    …significantly in the life sciences industry? Lonza AG is looking for a QA Manager - Raw Materials Compliance who demonstrates dedication to lead our hard-working ... Today, Lonza is a global leader in life sciences operating across five...role involves providing strategic and tactical guidance, maintaining impeccable compliance and quality standards within our rapidly expanding organization.… more
    Upward (07/14/25)
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  • CMA CGM (Chicago, IL)
    compliance and alignment with the Business. Ensure full adherence and compliance to applicable standards , regulation and Global Quality Framework and ... CEVA Logistics provides global supply chain solutions to connect people, products,...team to support and ensure CEVA North America-Sites full compliance with requirements established on CEVA Quality Management System.… more
    Upward (07/06/25)
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  • Abbott (Altavista, VA)
    Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of ... help nourish millions of families around the world. The Food Safety Manager will be responsible for establishing and maintaining best-in-class food safety culture… more
    Upward (07/10/25)
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  • Takeda Pharmaceutical Company Limited (Round Lake, IL)
    …computer system validations. You will report to the Quality Validation Manager . How you will contribute: Quality Systems/Document Control: Owns Standard Operating ... Validation Maintenance packages following existing procedures. Review deliverables for compliance to existing requirements. Approve validation documentation (eg, protocols,… more
    Upward (07/26/25)
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  • Abbott (Tipp City, OH)
    Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of ... Finance, Productivity and People Lead efforts required to deliver quality and compliance performance for the shift. Initiate, manage, and make decisions which impact… more
    Upward (07/11/25)
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  • Enovis (Fort Worth, TX)
    …patient care and creating better patient outcomes. Job Title: Manager , Quality Assurance Reports To: Director, Quality Assurance-Recovery Sciences Location: ... QA - LiteCure Job Title/High-Level Position Summary: The Quality Assurance Manager is responsible for managing, developing, implementing, and maintaining technical… more
    Upward (07/16/25)
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  • Arxada (Conley, GA)
    Arxada is a global specialty chemicals business that's committed to solving the world's toughest preservation challenges through better science. [With a proud ... social change through the development of cleaner, greener solutions. The Quality Manager will provide leadership to support the Quality Management System (QMS) in… more
    Upward (07/04/25)
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  • Cipla (Fall River, MA)
    …and efficient execution of their job duties, while ensuring product compliance to established standards. Essential Duties and Responsibilities *Dispensing raw ... of pharmaceutical manufacturing and related documents. *Basic understanding of deviation, CAPA , change control, FMECA , OOS,OOT and OOAC. Other Responsibilities… more
    Upward (07/12/25)
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  • Cipla (Fall River, MA)
    …- 5:00PM (may vary based on business needs) Reports To : Manufacturing Manager Salary Range: $62,400 - $75,400 Purpose: The content and statements documented in ... Manufacturing/Packaging and partners with cross functional team members to ensure compliance and operational success through user focused documentation at InvaGen… more
    Upward (07/20/25)
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  • Michael Page (Yonkers, NY)
    …Engineer to join the team due to growth. This position will report into the Quality Manager and will work at the 350+ employee site on a team of strong quality ... for the following: Develop, implement, and maintain quality processes and documentation in compliance with FDA 21 CFR Part 820 and ISO 13485 Perform and document… more
    Upward (07/26/25)
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  • Solugenix (Carlsbad, CA)
    …opportunity in Carlsbad, CA (Onsite). Under the supervision of the Quality Department Manager , the Quality Engineer will assist in coordination of internal audits as ... in all client sites. Manage all Quality Management system activities including CAPA , Management Review, and Document Control. Conduct failure analysis on returned… more
    Upward (07/18/25)
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  • Senior Manager , CAPA

    Catalent Pharma Solutions (Harmans, MD)
    …meetings, and communication of CAPA -related metrics to key stakeholders. The CAPA Manager will collaborate with cross-functional teams to ensure quality ... **Senior Manager , CAPA ** **Summary:** _Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to… more
    Catalent Pharma Solutions (07/04/25)
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