• Global Quality Lead

    Sanofi Group (Morristown, NJ)
    **Job Title:** Global Quality Lead , GMP , GDP Audit and Inspection - Pipeline Launch **Location:** Framingham, MA or Morristown, NJ **About the Job** We ... in Sanofi. + **Scope:** Manufacturing & Supply, Research & Development, Countries, Digital, Global Quality organizations in Sanofi. And third parties outside of… more
    Sanofi Group (07/11/25)
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  • INSPECTOR (swing shift)

    Berry Global (Monroe, NJ)
    …by First Article and In-Process Inspection procedures and assigned by the Lead Inspector. Follow all work instruction related to in process inspection. 3.2 ... Conduct daily dimension as required by department procedures, or Lead Inspector. 3.3 Clearly document Inspection results on Inspection sheets maintaining GMP more
    Berry Global (05/14/25)
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  • Specialist, Quality Assurance - Hybrid

    Merck (Rahway, NJ)
    …assigned projects including clinical supply disposition commitments and maintenance of a current GMP posture within Global Development Quality . + Adhere to ... worldwide regulations and our Company procedures. They will also collaborate with the Quality Program Lead to issue reports summarizing results, works with area… more
    Merck (07/12/25)
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  • Lead Project Engineer, Equipment…

    Bristol Myers Squibb (Summit, NJ)
    …better place than here at BMS with our Cell Therapy team. The ** Lead Project Engineer, Equipment Commissioning and Qualification (ECQ)** Delivery, plays a key role ... to meet business needs in accordance with required schedules or dates. + Lead and oversee contract project teams to ensure timely execution and adherence to… more
    Bristol Myers Squibb (07/03/25)
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  • Global Director, Continuous Improvement

    Catalent Pharma Solutions (Somerset, NJ)
    **Job Title: Global Director, Continuous Improvement** **Location: Bridgewater, NJ** **Position Summary** The focus of this role will be identifying and implementing ... and late-stage clinical products efficiently, timely, and with high quality . Scope of the role covers the entire product...delivery of the cost transformation across the company. The Global Director Continuous Improvement will be part of the… more
    Catalent Pharma Solutions (07/08/25)
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  • Associate Director, Technical Operations…

    Bristol Myers Squibb (Summit, NJ)
    …as the Global Technical SME for Drug Product and Vector Validation. The lead will develop global technical standards for cell therapy validation and deploy ... providing SME assessment for proposed process life-cycle changes. The lead will serve as the Global Point...global cell therapy validation technical standards via the quality system. + Promote innovative and efficient approaches to… more
    Bristol Myers Squibb (06/26/25)
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  • Plant Engineer Lead

    Lilly (Branchburg, NJ)
    …to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work ... we do, to achieve our mission of Making Medicine with Safety First & Quality Always; following our common purpose under TEAM Lilly and our Manufacturing Standards… more
    Lilly (07/10/25)
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  • Compliance Head, US FDA

    Sanofi Group (Morristown, NJ)
    …and high- quality responses and support the development and promotion of Global Quality Documentation. + Supports the preparation, execution and closure of ... purposes, and ensuring accurate reporting to Operations Management and Global Quality . . **Core member of critical.... . **Core member of critical governance** + Sanofi's GMP GDP Quality Council to facilitate sharing… more
    Sanofi Group (06/03/25)
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  • Senior Team Lead 2nd Shift

    dsm-firmenich (Somerset, NJ)
    **Sr. Team Lead 2nd Shift, Production, PE** **Somerset, NJ, US** This position will lead and coordinate and manage the 3rd shift Production Team, providing ... implementing process improvement initiatives. + Conduct daily audits of Quality Risk Assessments, proactively addressing and preventing non-conformances and utilize… more
    dsm-firmenich (07/09/25)
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  • Lead Engineer, CSV

    Bristol Myers Squibb (Summit, NJ)
    …place than here at BMS with our Cell Therapy team. The ** Lead Computer System Validation (CSV) Engineer** supports the successful implementation of manufacturing ... while promoting a positive learning, team environment. + Author quality procedures and training documents. + Deliver training on...office environment. Will be required to enter laboratory or GMP process areas donning proper gowning / lab coats… more
    Bristol Myers Squibb (07/08/25)
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  • Lead Contracts Manager - Data Center…

    Meta (Trenton, NJ)
    **Summary:** Meta seeks highly engaged and experienced team players for lead roles to join our Design, Engineering & Construction (DEC) organization to direct ... join a high-powered team of industry leaders! **Required Skills:** Lead Contracts Manager - Data Center Design, Engineering &...team, peers, and outside business units to enhance the quality and efficiency of contracting processes 12. Ensure all… more
    Meta (06/25/25)
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  • Quality Control Supervisor

    Kelly Services (Skillman, NJ)
    …and biotechnology industry, specializing in ** Quality Control (QC), Quality Systems, Analytical Method Validation** , and ** Global Specification ... authoring and reviewing documentation in systems such as **TrackWise** and **Veeva Vault Quality Docs** . + Lead the **digital transformation of QC systems**… more
    Kelly Services (07/12/25)
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  • Associate Director, CAR-T Manufacturing Operations

    Bristol Myers Squibb (Summit, NJ)
    …Science & Technology, QC Laboratories, QA Doc Control, Training & Learning Organization, Global manufacturing departments, Global Quality and Global ... to achieve results while creating an engaging, accountable, and learning culture. ** GMP ** + Is accountable to ensure their Manufacturing Sr. Managers, Managers and… more
    Bristol Myers Squibb (07/10/25)
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  • Quality Specialist

    Astrix Technology (New Brunswick, NJ)
    …assist with additional duties. **Qualifications** + Bachelor's degree + 3 years in Quality Assurance or manufacturing in GMP -regulated industry + Proficiency in ... ** Quality Specialist** Quality Assurance Middlesex County,...Added - 01/07/2025 Apply for Job Our Client, a global nonprofit organization on the forefront of saving and… more
    Astrix Technology (07/02/25)
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  • Associate Director Quality Assurance…

    BeOne Medicines (Pennington, NJ)
    …Chain, Technical and Operational departments frequently. + Interacts with BeiGene Global Quality . **Supervisory Responsibilities:** + This position includes ... some travel. **_Essential Functions of the job_** **_:_** + Within the Quality Assurance organization, develop and implement Compliance programs for the Hopewell, NJ… more
    BeOne Medicines (05/08/25)
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  • Quality Specialist

    Kelly Services (Somerset, NJ)
    …throughout all project phases. + Organize and review system-related documentation for quality and regulatory alignment. Lead or assist with **user training ... **Job Title: eQMS Implementation Specialist** **Department: Quality Assurance** **Location:** Somerset NJ **Position Summary:** The **eQMS Implementation… more
    Kelly Services (07/01/25)
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  • Senior Director, Cell Therapy Supply Chain

    Bristol Myers Squibb (Summit, NJ)
    …a state of compliance across all supply chain operations, ensuring adherence to GMP and internal quality standards. + Drive continuous improvement initiatives, ... Day Shift, 8 am - 5 pm **Responsibilities:** + Lead end-to-end planning processes across the site, including inbound...management, and master data functions. + Partner with manufacturing, quality , engineering, IT, and global supply chain… more
    Bristol Myers Squibb (07/04/25)
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  • Principal Analytical Technical Steward-API EM

    Lilly (Branchburg, NJ)
    …The Analytical Technical Steward works closely with development counterparts and GQL ( Global Quality Laboratories) to ensure robust analytical control strategies ... facilitate updating packages as needed. + Participates in method validations according to Global Quality Standards (either to bring methods up to current… more
    Lilly (07/10/25)
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  • Director, Small Molecule AR&D, Raw Materials…

    Merck (Rahway, NJ)
    …creativity, effective interpersonal and collaborative skills + Demonstrated ability to lead teams to deliver high- quality results against firm deadlines ... technologies and predictive analytical tools. As part of our global team, you will have the opportunity to collaborate...the Raw Materials and Medical Devices/Combination Products (MDCP) will lead a team of specialists and scientists in Rahway… more
    Merck (06/18/25)
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  • Auditing & Compliance Director - Software as…

    Wolters Kluwer (New York, NY)
    …month in the office (see approved locations on the posting). **OVERVIEW** You will be the global product quality lead in support of a broad portfolio of ... + Manage and guide system testing activities, including verification and validation. + Lead resolution of quality issues with on-market device software; drive… more
    Wolters Kluwer (06/11/25)
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