• Novo Nordisk Inc. (West Lebanon, IN)
    …Quality assurance / GMP and Validation: Maintain qualified state of GxP IT Infrastructure platform at Site , providing input, review, and hands-on in relevant ... IT Operations Service delivery and Incident Management at Site , being recognized as the single point of contact...IT Operations advocate, coordinating daily activities with the IT Manager ( IT Infrastructure Owner)… more
    HireLifeScience (04/09/24)
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  • Novo Nordisk Inc. (Durham, NC)
    …implementation & maintenance of processes, equipment & utilities for the Site . Provide comprehensive validation subject matter expertise. Establish & maintain good ... in accordance with the Novo Nordisk Way. Relationships Senior Manager . Essential Functions Maintain plans to meet changes in...evolve the science and risk-based validation program for the Site in accordance with NN procedures & local requirements… more
    HireLifeScience (05/01/24)
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  • Novo Nordisk Inc. (Durham, NC)
    …Cycle Management (Mdev LCM) in Emerging Technologies (ET) for the production site . Lead strategic activities ensuring new products can thrive without disrupting the ... performance Drive Mdev LCM and QA requirements at the site ensuring a high level of communication & collaboration...capable to meet quality specifications & requirements, to include GMP Compliance of the team Ensure appropriate support is… more
    HireLifeScience (05/03/24)
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  • Novo Nordisk Inc. (West Lebanon, IN)
    About the Department Site New Hampshire, located in West Lebanon, is where Novo Nordisk's life-saving treatments are brought to life. Our manufacturing facility ... as our next generation of cutting-edge medications. It's not your average production site - it's a tight-knit, supportive community working together to contribute to… more
    HireLifeScience (05/02/24)
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  • Novo Nordisk Inc. (West Lebanon, IN)
    About the Department Site New Hampshire, located in West Lebanon, is where Novo Nordisk's life-saving treatments are brought to life. Our manufacturing facility ... as our next generation of cutting-edge medications. It's not your average production site - it's a tight-knit, supportive community working together to contribute to… more
    HireLifeScience (03/20/24)
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  • FUJIFILM Holdings America Corporation (Holly Springs, NC)
    …United States. External US About This Role The Manager , QC Raw Materials Manager is accountable for GMP compliant laboratory operations according to GMP ... than $2 billion into establishing a new large-scale manufacturing site for biopharmaceuticals in the United States to accelerate...GMP and all reported results are accurate. The Manager , QC Raw Materials is the technical subject matter… more
    JobGet (05/05/24)
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  • FUJIFILM Holdings America Corporation (Holly Springs, NC)
    …in Holly Springs, North Carolina, United States. External US About the RoleThe Manager , QC Chemistry is accountable for GMP compliant laboratory operations ... than $2 billion into establishing a new large-scale manufacturing site for biopharmaceuticals in the United States to accelerate...GMP , and all reported results are accurate. The Manager , QC Chemistry is the technical subject matter expert… more
    JobGet (05/05/24)
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  • FUJIFILM Holdings America Corporation (Holly Springs, NC)
    …operational aspects of the QC group at Fujifilm Diosynth Biotechnologies. The Manager , Bioassay/Virology is accountable for GMP compliant laboratory operations ... are investing more than $2 billion into establishing a new large-scale manufacturing site for biopharmaceuticals in the United States to accelerate the growth of our… more
    JobGet (05/05/24)
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  • Manager , IT

    ThermoFisher Scientific (Greenville, NC)
    …leadership to drive efficient technology solutions. **What will you do?** + Lead the IT Site Service Function for Pharma Services. The primary services delivered ... audits, investigations, and CAPA. + Key contact to support site capital projects and act as IT ...related work experience. + Demonstrable experience with GxP regulations ( GMP , GLP, GCP), CFR 21 Part 11, and IEC… more
    ThermoFisher Scientific (04/14/24)
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  • Manager , IT Operations & Support

    Novo Nordisk (Clayton, NC)
    …levels across the organization, as well as in DK + Develop strategic direction for site IT assets, monitor advancements in the industry & recommend & implement ... support to the site . Provides information to site leadership on IT issues, plans, projects...from an accredited university with eight (8) years of IT or automation experience, preferably in a GMP more
    Novo Nordisk (05/04/24)
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  • Senior IT Automation Engineer

    Bristol Myers Squibb (Phoenix, AZ)
    …more: careers.bms.com/working-with-us **Position Summary** The Senior Engineer, Information Technology ( IT ) Manufacturing - Automation reports to the Manager ... Completes deliverables during the design, delivery, commissioning of good manufacturing practices ( GMP ) computerized systems at the Phoenix site . + Provides… more
    Bristol Myers Squibb (05/03/24)
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  • Senior Manager , Site Facilities…

    Bristol Myers Squibb (Summit, NJ)
    …opportunities uncommon in scale and scope. **Position Summary** As the Senior Manager of Utilities and Building Automation Systems (BAS) Operations, your primary ... liaison with Global Capital Project Engineering for successful execution of site infrastructure projects, ensuring proper commissioning and turnover + Drive… more
    Bristol Myers Squibb (05/04/24)
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  • Senior Manager , Site Finance Lead

    Teva Pharmaceuticals (Forest, VA)
    Senior Manager , Site Finance Lead - Forest, VA Date: Apr 26, 2024 Location: Forest, United States, Virginia, 24551 Company: Teva Pharmaceuticals Job Id: 53866 ... of progressive experience in Finance/Accounting is required + Manufacturing site experience is required; pharmaceutical/food/consumer health goods (FDA/ GMP )… more
    Teva Pharmaceuticals (05/01/24)
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  • Senior Manager , Quality Control - West…

    Teva Pharmaceuticals (West Chester, PA)
    Senior Manager , Quality Control - West Chester, PA (On- site ) Date: May 4, 2024 Location: West Chester, United States, Pennsylvania, 19380 Company: Teva ... make a difference with. **The opportunity** As a Senior Manager of Quality Control you will manage a quality...and maintain local, regional and global regulatory compliance (ICH, GMP , EPA, OSHA, etc.), and supervise resources and assets… more
    Teva Pharmaceuticals (04/06/24)
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  • Senior Manager Validation, Engineering…

    Bristol Myers Squibb (Bothell, WA)
    …lives. Read more: careers.bms.com/working-with-us . **Position Summary** The Senior Manager , Validation, Engineering and Technology is responsible for supporting the ... the Bristol Myers Squibb Manufacturing Plant (Jump), Bothell, WA. The Senior Manager oversees the Right to Operate, Operational Excellence and Ongoing Monitoring… more
    Bristol Myers Squibb (04/30/24)
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  • Manager , Quality Auditing (Post Audit)

    Regeneron Pharmaceuticals (Troy, NY)
    …external audit programs and may perform external audits for Regeneron, with primary emphasis on GMP , IT and Quality audits that may impact GMP operations ... We are currently looking to fill a Manager , Quality Auditing (Post Audit) position. This position...typical day might include the following: + Leads the GMP Auditing's Post-Audit Team who is responsible for evaluating… more
    Regeneron Pharmaceuticals (04/24/24)
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  • IT Infrastructure Analyst II (Onsite)

    Novo Nordisk (West Lebanon, NH)
    …needs + Acts as IT Operations advocate, coordinating daily activities with the IT Manager ( IT Infrastructure Owner) and team members + Assists the ... IT Operations Service delivery and Incident Management at Site , being recognized as the single point of contact...interactions with others + Other duties outlined by the IT Manager (Infrastructure Owner) Physical Requirements This… more
    Novo Nordisk (04/09/24)
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  • Associate Project Manager

    Integra LifeSciences (Cordova, TN)
    …help improve outcomes. The **Associate Project Manager ** will be reporting to the Site Manager in Memphis TN. The primary purpose of the Associate Project ... facility. **SUPERVISION RECEIVED** Under the direct supervision of the Site Manager or Continuous Improvement Manager...in a medical device manufacturing environment.** **.Experience in new GMP site startup, GMP commissioning… more
    Integra LifeSciences (03/23/24)
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  • Manager - MES System Analyst

    Lilly (Concord, NC)
    …Lilly is investing over $1 billion to create a new state-of-the-art manufacturing site , in Concord, North Carolina. The brand-new facility will utilize the latest ... once-in-a-lifetime opportunity to help build and operate a new site . The Lilly Concord site will be...activities to meet quality and compliance standards. Experience with GMP regulations. + Ensure MES system is in compliance… more
    Lilly (02/20/24)
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  • Manager QA Distribution

    Charles River Laboratories (Memphis, TN)
    Manager QA Distribution Req ID #: 221948 Location: Memphis, TN, US, 38118Memphis, TN, US, 38118 For 75 years, Charles River employees have worked together to assist ... globe. Whether your background is in life sciences, finance, IT , sales or another area, your skills will play...that you can feel passionate about. **Job Summary** The Manager QA Distribution reports to the Director Quality Assurance.… more
    Charles River Laboratories (03/14/24)
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