• Legend Biotech USA, Inc. (Raritan, NJ)
    …and productivity.Key Responsibilities Co-Lead Deviation Investigations: Collaborate closely with the Quality Associate Director to co-lead the deviation ... in the treatment of multiple myeloma. Legend Biotech is seeking an Associate Director for Operations Compliance and Investigations Managementas part of… more
    HireLifeScience (04/19/24)
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  • Merck & Co. (Rahway, NJ)
    …reliance on automation within Biologics Process Research & Development (BPR&D).The Associate Director role-will provide process automation leadership within the ... projects, work to design, install, and qualify new equipment to support GMP clinical production. -Execute and develop appropriate system validation, change control,… more
    HireLifeScience (05/14/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …other research areas centered around rare diseases and immune disorders.Summary The Associate Director , RACMC Portfolio Products, will be responsible for ... that CMC documentation is complete, well organized, scientifically sound, of a high quality , aligned with the current regulations, and presented in a manner that… more
    HireLifeScience (03/01/24)
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  • Merck & Co. (Rahway, NJ)
    …of engineering fundamentals. The MACS Operations Specialist position will report to the Director , Engineering and will be a member of the EF Team at the ... the Operations Specialist include the following:The Operations Specialist role at the Associate Specialist level will serve as a process team member supporting the… more
    HireLifeScience (05/21/24)
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  • Merck & Co. (Rahway, NJ)
    …and project management responsibility. The Specialist -Engineering position will report to the Associate Director , Engineering and will be a member of the EF ... and equipment in the facility are ready for the GMP and non- GMP work that the scientists...safety partners and other team members to ensure the quality and safe delivery of clinical supplies, and ultimately… more
    HireLifeScience (05/22/24)
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  • Associate Director , External…

    Amicus Therapeutics (Princeton, NJ)
    Associate Director , External Quality Lead (Small Molecule) Location Princeton, NJ Requisition ID 2258 # of openings 1 Apply Now ... (https://phh.tbe.taleo.net/phh04/ats/careers/v2/applyRequisition?org=AMICUS&cws=37&rid=1303) Associate Director , External Quality Lead (Small Molecule)… more
    Amicus Therapeutics (05/04/24)
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  • Associate Director Quality

    Merck (Rahway, NJ)
    …(include Requirements For Education, Experience And Skills)** + **Job Description:** The Associate Director Quality Assurance, Facilities, Validation & ... Automation will provide Quality Assurance oversight and support to GMP facilities, equipment, and laboratories within our Research & Development Division… more
    Merck (05/23/24)
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  • Automation Associate Director

    Merck (Rahway, NJ)
    …reliance on automation within Biologics Process Research & Development (BPR&D). The Associate Director role will provide process automation leadership within the ... projects, work to design, install, and qualify new equipment to support GMP clinical production. + Execute and develop appropriate system validation, change control,… more
    Merck (05/14/24)
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  • Associate Director , Clinical Supply…

    J&J Family of Companies (Titusville, NJ)
    Associate Director , Clinical Supply Integrator - 2406179836W **Description** Johnson & Johnson is recruiting for an ** Associate Director , Clinical Supply ... health for humanity. Learn more at https://www.jnj.com/ . The Associate Director , is a matrix team leader...particular trial and for various processes during GCP and GMP health authority inspections. + Provide mentorship and support… more
    J&J Family of Companies (05/16/24)
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  • Senior Scientist/ Associate Director

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …research areas centered around rare diseases and immune disorders. **Summary** The Associate Director , RACMC Portfolio Products, will be responsible for ... that CMC documentation is complete, well organized, scientifically sound, of a high quality , aligned with the current regulations, and presented in a manner that… more
    Daiichi Sankyo Inc. (04/12/24)
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  • Director , Plant Operations

    Promotion In Motion (Somerset, NJ)
    …there is a quality staff, it is the ultimate responsibility of the Director , Plant Operations to ensure quality products are produced that meet both ... Director , Plant Operations Job Details Job Location Somerset...all business results for the operation including productivity, safety, quality , cost, and organizational development. DUTIES AND RESPONSIBILITIES +… more
    Promotion In Motion (03/08/24)
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  • Associate Specialist - MACS Operations…

    Merck (Rahway, NJ)
    …of engineering fundamentals. The MACS Operations Specialist position will report to the Director , Engineering and will be a member of the EF Team at the ... the Operations Specialist include the following: The Operations Specialist role at the Associate Specialist level will serve as a process team member supporting the… more
    Merck (05/21/24)
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  • Specialist - Engineer

    Merck (Rahway, NJ)
    …and project management responsibility. The Specialist -Engineering position will report to the Associate Director , Engineering and will be a member of the EF ... and equipment in the facility are ready for the GMP and non- GMP work that the scientists...safety partners and other team members to ensure the quality and safe delivery of clinical supplies, and ultimately… more
    Merck (05/22/24)
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  • Manager - Warehouse Operations

    Lilly (Branchburg, NJ)
    …world. #WeAreLilly **Position Overview:** The Manager - Warehouse reports to the Associate Director -Warehouse and is responsible for technical support for ... perform a wide variety of support activities and functions while supporting a GMP manufacturing facility. This role will be responsible for assuring compliance with… more
    Lilly (05/12/24)
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  • Senior Training Specialist, Operations

    Integra LifeSciences (Plainsboro, NJ)
    …to review document curriculums and ensure they are mapped to the appropriate associate . + Working with Document Control Team, Quality , and Manufacturing ... of experience. + Adequate knowledge of learning management software. + Experience in GMP and quality systems regulations (ISO 13485:2016, CFR 820). + Proven… more
    Integra LifeSciences (04/19/24)
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  • Clinical Supply Manager

    Actalent (Paramus, NJ)
    Job Description: + Assist and support the Associate Director in managing Contract Development and Research Organizations (CDMO) in the areas of Clinical ... documents for their submissions (US and Global). + Assist and support the Quality Assurance Unit (QAU) regarding the review of investigations and conduct vendors and… more
    Actalent (05/16/24)
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