• Merck & Co. (Durham, NC)
    Job DescriptionThe Quality Associate Director/ GMP Lead Site Auditor will have leadership responsibility for the site internal audit program, encompassing the ... achieve excellence and ensure program is effective.- The position requires ability to lead and perform the operational aspects of the audit program, apply risk-based… more
    HireLifeScience (12/11/25)
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  • Post Holdings Inc. (Klingerstown, PA)
    …contractors while they are onsite to include human safety, food safety, and plant GMP requirements. + Lead department team members to ensure personal safety, ... in all jobs and tasks. + Adheres to quality work practices, follows GMP 's, maintains sanitary conditions and ensures that product quality is maintained. Reports on… more
    DirectEmployers Association (11/20/25)
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  • Coty (Sanford, NC)
    …todrive high-impact capital projects, leveraging advanced automation, hygienic design, and GMP standards. Lead innovation in beauty manufacturing with ... for capacity expansion, cost optimization, and safety enhancement. You will lead cross-functional engineering initiatives to deliver impactful capital projects that… more
    DirectEmployers Association (11/07/25)
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  • Kerry (Melrose Park, IL)
    …transportation and dock operations. + Drive safety, food safety, and compliance with OSHA, GMP , and company standards. + Lead and develop a multi-shift team of ... environment. About the role We are seeking an experienced Warehouse Manager to lead all warehouse, yard, and material-flow operations at our Melrose Park food… more
    DirectEmployers Association (11/27/25)
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  • BeOne Medicines (Pennington, NJ)
    …operations. + Review, interpret, and report analytical data in accordance with GMP regulations and internal procedures. + Lead troubleshooting efforts for ... a primary focus on capillary electrophoresis techniques to support GMP manufacturing, testing, and release of material, intermediates and...for the laboratory. + Participate in internal and external GMP audits, as needed. + Train analysts and new… more
    DirectEmployers Association (09/30/25)
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  • Endo International (Hobart, NY)
    …documents such as batch records, quality agreements, SOPs, etc. + Actively takes the lead in ensuring GMP compliance for the company. Sets strategy in ... + Extensive knowledge of FDA regulatory requirements applicable to pharmaceuticals. Applies GMP regulations and other international guidelines to all aspects of the… more
    DirectEmployers Association (12/12/25)
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  • Post Holdings Inc. (Chaska, MN)
    …change. 6. Communicating all process inefficiencies, equipment malfunctions, safety concerns and GMP issues to the department Lead and/or Supervisor 7. Adhere ... to safe work practices, follow GMP 's, maintain sanitary conditions and ensure that product quality is maintained. Report to management any conditions or practices… more
    DirectEmployers Association (12/11/25)
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  • BeOne Medicines (Pennington, NJ)
    …to day operations of the Biochemistry laboratory. **Essential Functions of the job:** + Lead the QC Biochemistry GMP laboratory through late phase activities. + ... Supervises staff and executes QC Biochemistry laboratory activities to support GMP manufacturing, testing and release of material, intermediates and finished… more
    DirectEmployers Association (09/19/25)
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  • Post Holdings Inc. (Battle Creek, MI)
    …and safe working condition while meeting all regulatory requirements. - Perform safety, GMP , and pre-operational audits. - Lead and drive continuous improvement ... food safety and quality practices as required through SQF and GMP 's. **Qualifications** **Leadership Competencies:** Organizing, planning, drive for results, action… more
    DirectEmployers Association (10/11/25)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …with other QA functions and/or applicable stakeholders. Support/ lead and or co lead due- diligence assessments of GMP facilities and or CMOs as deemed ... disorders. Summary: Accountable to organize and directs an audit universe for GMP relevant activities involving but not limited to supplier qualification program,… more
    HireLifeScience (12/05/25)
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  • Legend Biotech USA, Inc. (Raritan, NJ)
    …in the treatment of multiple myeloma.Legend Biotech is seeking a Quality Systems Lead as part of the Quality team based in Raritan, NJ. Role OverviewThe ... Quality Systems Lead role is an exempt level position with responsibilities...support both clinical and commercial requirements in a sterile GMP environment. This role will serve as the business… more
    HireLifeScience (11/06/25)
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  • Merck & Co. (Rahway, NJ)
    …both in terms of facility construction and organizational realization. The GMP facility is designed for multi-product operations with flexible operating suites, ... new technologies, trialing new automation strategies, and implementing them in the GMP areasSupport capital projects, work to design, install, and qualify new… more
    HireLifeScience (12/05/25)
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  • Legend Biotech USA, Inc. (Raritan, NJ)
    …an immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking QA Investigations Lead I as part of the Quality team based in Raritan, NJ. Role ... OverviewThe QA Investigation Lead is an exempt level position reporting to the...of a personalized cell therapy product in a sterile GMP environment. The ideal candidate for this role demonstrates… more
    HireLifeScience (11/12/25)
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  • Dr. Reddy's Laboratories (Princeton, NJ)
    …options to satisfy unmet medical needs, we are dedicated to helping people lead longer and healthier lives. We are seeking dynamic and energetic individuals ready ... background. **Job Description** **Job Summary** We are looking for a seasoned Lead Associate, Quality Audits professional who will conduct assessment on company… more
    DirectEmployers Association (11/06/25)
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  • Legend Biotech USA, Inc. (Raritan, NJ)
    …an immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking QA Investigations Lead III as part of the Quality team based in Raritan, NJ. Role ... OverviewThe QA Investigations Lead is responsible for providing quality oversight over the...support both clinical and commercial requirements in a sterile GMP environment. This includes supporting and approving manufacturing investigations,… more
    HireLifeScience (10/17/25)
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  • Curia (Rensselaer, NY)
    …and the preparation of CAPAs and monitor the completion of assigned tasks. + Lead and drive the GMP activities, work with manufacturing Managers and supervisors ... + Manage all the customer audits at the site, lead the preparation of CAPAs, and monitor their completion...regulations (eg, 21 CFR 11, 210, 211, 820, EU GMP , ICH Q7), Quality Systems for active pharmaceutical ingredients… more
    DirectEmployers Association (09/24/25)
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  • ValSource, Inc. (Worcester, MA)
    …technically skilled leaders in Process/Process Equipment Engineering to support exciting GMP Drug Substance and Drug Product capital projects throughout our network ... our clients’ Process Engineering programs within Pharmaceutical and Biotech GMP manufacturing facilities. This includes systems and equipment used...to act in the best interest of the client. Lead the project through an offsite design effort (at… more
    HireLifeScience (10/28/25)
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  • Kerry (Blue Earth, MN)
    …and grow in a truly global environment. About the role The Production Lead is responsible for promoting safety awareness, producing high quality product, while ... Ensures that products are made in sanitary conditions and GMP practices are being followed. ? Assign GMP...vacations and personal time as well as covering additional lead tasks. ? Document and collect all daily production… more
    DirectEmployers Association (10/29/25)
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  • Post Holdings Inc. (Britt, IA)
    …- Adhere to all safety policies and procedures. - Detect and correct GMP /Safety violations. - Act upon employee issues. - Adhere to safe work practices, ... follow GMP 's & SQF policies, maintain sanitary conditions and ensure...EXPERIENCE REQUIRED: Education: No prior experience or training. Experience: Lead experience preferred. Language Skills: Ability to read and… more
    DirectEmployers Association (11/18/25)
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  • FreshRealm (Linden, NJ)
    …onsite in our Linden, NJ facility.** FreshRealm is looking for a Team Lead Inventory Control to be responsible for overseeing the activities of employees engaged ... team as a business by owning the team's quality, GMP and uniform standards, ensures that we send out...+ Tracks and escalates patterns and behaviors around timekeeping, GMP compliance, Quality and Performance to Supervisor/Leadership + Coaches… more
    DirectEmployers Association (11/05/25)
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