• Associate Director , MACS…

    Merck (Rahway, NJ)
    …job that provides a high degree of technical and project management responsibility. The Associate Director - Process/Facility Lead position will report to the ... infrastructure. Responsibilities include the following: The process/facility lead role at the Associate Director level will serve as a technical mentor and… more
    Merck (09/18/24)
    - Save Job - Related Jobs - Block Source
  • Associate Director , Analytical…

    BeiGene (Hopewell, NJ)
    **_General Description:_** Manages QC analytical activities to support GMP manufacturing, including testing and release of raw materials, intermediates and finished ... International Regulations and BeiGene processes procedures. Develops and implements quality control processes and procedures and supports regulatory compliance… more
    BeiGene (07/10/24)
    - Save Job - Related Jobs - Block Source
  • Associate Director , Quality

    Sanofi Group (Morristown, NJ)
    ** Associate Director , Quality - US Consumer Healthcare (CHC)** Location: Morristown, NJ **_About the Job_** If you're driven by a commitment to excellence, ... in our mission to uphold the highest standards of quality and make a positive impact on the lives...GMP Regulatory Compliance, including Regulatory audits + Certified Quality Auditor preferred + Continuous Improvement Management, Quality more
    Sanofi Group (09/15/24)
    - Save Job - Related Jobs - Block Source
  • Associate Director , Compliance…

    Bristol Myers Squibb (Princeton, NJ)
    …lives. Read more: careers.bms.com/working-with-us . **Summary:** The position is for an Associate Director , Investigator in the Compliance & Ethics organization ... & Ethics objectives such as analytics, metrics sharing, and training. The Associate Director , Investigator will work both independently and collaboratively… more
    Bristol Myers Squibb (09/19/24)
    - Save Job - Related Jobs - Block Source
  • 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. (07/12/24)
    - Save Job - Related Jobs - Block Source
  • Director , Product Quality

    Burlington (Burlington, NJ)
    …largest off-price retailers in the nation, join Burlington Stores, Inc. team as a Director Product Quality . **Position Summary:** Lead the quality team ... product validation, sample review and approval.Drive development of product quality program in collaboration with Merchants and Supply Chain.... tools and techniques such as 6 Sigma, Lean, GMP , QMS or similar **Skills and Abilities:** + Ability… more
    Burlington (09/20/24)
    - Save Job - Related Jobs - Block Source
  • 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 (09/21/24)
    - Save Job - Related Jobs - Block Source
  • Senior Quality Engineer

    BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
    **Job Description Summary** As directed by the Associate Director , the Sr. Quality Engineer is accountable for supporting new product development and product ... maintenance through the application of Quality engineering skills for medical devices. This person will...Risk Management preferred + Familiarity with Good Manufacturing Practices ( GMP ) and Design Controls processes desired + Experience conducting… more
    BD (Becton, Dickinson and Company) (09/18/24)
    - Save Job - Related Jobs - Block Source
  • 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 (09/12/24)
    - Save Job - Related Jobs - Block Source