• Aequor (Bothell, WA)
    …presence within a regulated cGMP environment. The primary focus of the QA Specialist role will be to support routine clinical and commercial production ... providing direct training , guidance, and problem solving to peers. Provide training , coaching, and feedback for GMP guidance. Continue support of continuous… more
    HireLifeScience (05/03/24)
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  • Merck & Co. (Rahway, NJ)
    …multi-modality (small molecule, macrocyclic peptides, bioconjugates) Drug Substance development and GMP clinical manufacturing plant currently planned in Rahway, ... enabling gain of critical internal experience with scale-up of manufacturing GMP steps, demonstration of new manufacturing technology/processes, training more
    HireLifeScience (04/24/24)
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  • Catalent (Manassas, VA)
    POSITION SUMMARYThe Quality Assurance Specialist I is responsible for inspection and verification of the products and production processes along all the production ... compliance to FDA and cGMP standards for Quality Control, including continuous training . Perform cleaning verification by ATP, EMP testing; Conduct AQL inspections… more
    HireLifeScience (05/10/24)
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  • Catalent (Manassas, VA)
    …to help create engaging new products consumers will love.The Quality Assurance Specialist I - Quarantine is responsible for auditing the products and processes ... to FDA and cGMP standards for Quality Control, including continuous training ; Responsible for ensuring Dietary Supplement's Identity, Purity, Strength and Quality;… more
    HireLifeScience (04/16/24)
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  • Catalent (Manassas, VA)
    …to help create engaging new products consumers will love.The Document Control Specialist - 2nd Shift is responsible for creating and maintaining the Quality ... with FDA and cGMP standards for Quality Control, including continuous training ; Responsible for ensuring Dietary Supplement's Identity, Purity, Strength, and… more
    HireLifeScience (04/16/24)
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  • Dexian - DISYS (Bothell, WA)
    …presence within a regulated cGMP environment. The primary focus of the QA Specialist role will be to support routine clinical and commercial production ... experience, strong interpersonal skills *Job Description: The Quality Assurance Specialist position plays a key role in supporting the..., guidance, and problem solving to peers. * Provide training , coaching, and feedback for GMP guidance.… more
    JobGet (05/07/24)
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  • Clinical Research Quality Control…

    Kelly Services (Phoenix, AZ)
    ** Clinical Product Quality Specialist ** Kelly Science and Clinical is hiring for a temp-to-perm need for one of our clients who is a leading player in the ... 8-hour shifts) **Reporting To** : Quality Assurance Director **Position Summary:** The Clinical QA Specialist is responsible for administering routine quality… more
    Kelly Services (03/29/24)
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  • Clinical Cell Engineer Specialist II…

    MD Anderson Cancer Center (Houston, TX)
    …and/or Cellular Therapy treatment. **The ideal candidate will have GLP and/or GMP experience.** **KEY FUNCTIONS** 1. **Cell Manipulation and Processing** 1. Perform ... to procedures/policies implemented by internal or external study sponsors on various clinical trials that may differ from standard operating procedures of MDACC Cell… more
    MD Anderson Cancer Center (03/27/24)
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  • Principal Specialist , Quality Assurance…

    Editas Medicine (Cambridge, MA)
    …of internal clinical manufacturing at the Editas Waltham and Devens GMP manufacturing facilities as a member of the Quality Operations team. Specific ... Editas Devens GMP manufacturing facilities. Key Responsibilities: As the Principal Specialist , you will be responsible for: + Support Editas' clinical cell… more
    Editas Medicine (04/26/24)
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  • Senior DeltaV Specialist - Manufacturing…

    Merck (Rahway, NJ)
    …multi-modality (small molecule, macrocyclic peptides, bioconjugates) Drug Substance development and GMP clinical manufacturing plant currently planned in Rahway, ... enabling gain of critical internal experience with scale-up of manufacturing GMP steps, demonstration of new manufacturing technology/processes, training more
    Merck (04/24/24)
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  • Specialist Incoming, Sample Management…

    Bristol Myers Squibb (Bowdre, IL)
    …rules (EHS) as well as Good Documentation and Good Manufacturing Practices (GDP and GMP ). Finally, the QC Specialist Incoming is supporting activities related to ... complex GMP documentation such as standard procedures, work practices, training plans, and reports as result of deviation/investigation. **Maintain the GMP more
    Bristol Myers Squibb (04/20/24)
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  • Specialist QA

    Amgen (Thousand Oaks, CA)
    …oversight for global distribution and supply chain operations for commercial and clinical biopharmaceutical products. Ensure compliance to GMP regulations for ... deviation technical assessments or equivalent + Demonstrated ability to perform GMP operations including following detailed SOPs, maintaining training , and… more
    Amgen (05/05/24)
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  • Senior Specialist , Site Quality Systems

    Editas Medicine (Cambridge, MA)
    …of internal clinical manufacturing at the Editas Waltham and Devens GMP manufacturing facilities as a member of the Quality Operations team. Specific ... Editas Devens GMP manufacturing facilities. Key Responsibilities: As the Senior Specialist , you will be responsible for: + Supporting Editas' clinical cell… more
    Editas Medicine (04/26/24)
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  • Specialist , Quality Assurance Operations…

    Bristol Myers Squibb (Bothell, WA)
    …presence within a regulated cGMP environment. The primary focus of the QA Specialist role will be to support routine clinical and commercial production ... BMS with our Cell Therapy team. The Quality Assurance Specialist position plays a key role in supporting the..., guidance, and problem solving to peers. + Provide training , coaching, and feedback for GMP guidance.… more
    Bristol Myers Squibb (05/12/24)
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  • Document Control Specialist

    Bristol Myers Squibb (Indianapolis, IN)
    …assurance knowledge in maintaining the quality program to be ready for clinical development and GMP commercial operations. Additional responsibilities may ... lives. Read more: careers.bms.com/working-with-us . **Job Title:** **Document Control Specialist ** **Location:** **Indianapolis** This is an on-site position located… more
    Bristol Myers Squibb (05/10/24)
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  • Microbiology Lab Automation Applications…

    BD (Becton, Dickinson and Company) (Minneapolis, MN)
    …the Field Applications Specialist provides high-level technical and application training to BD Customers within clinical , public health, and industrial ... laboratory settings. This position has a primary focus on training in diverse settings; promoting sales of BD instrumented platforms and total system solutions, and… more
    BD (Becton, Dickinson and Company) (04/05/24)
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  • Quality Specialist

    Kelly Services (West Hills, CA)
    …in all their actions. + Complete all required trainings in a timely manner. + Attend GMP training as appropriate for the role. + Adhere to strict compliance with ... Quality Control Technician The Quality Specialist will maintain quality assurance programs, procedures and...related QA or QC experience required, experience in a GMP regulated environment is preferred. + Previous experience reviewing… more
    Kelly Services (04/04/24)
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  • Quality Assurance Specialist

    Bristol Myers Squibb (Indianapolis, IN)
    …quality assurance knowledge in ensuring compliance in operations to support clinical development and GMP commercial operations. Additional responsibilities may ... their personal lives. Read more: careers.bms.com/working-with-us . The Quality Assurance Specialist will help support operations through quality oversight in a new… more
    Bristol Myers Squibb (05/07/24)
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  • Associate Specialist , Label Print…

    Merck (West Point, PA)
    …production tasks for their appropriate areas in a Good Manufacturing Practices ( GMP ) manner under direction from Supervisors. Able to identify appropriate tasks and ... perform all functions independently without additional guidance or supervision after training . Able to learn and perform more complex tasks related to the function… more
    Merck (05/08/24)
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  • QC Specialist III Microbiology

    Charles River Laboratories (Memphis, TN)
    …a clear understanding of Microbiological sampling/testing concepts, lean principles, GMP training program requirements, and laboratory equipment requirements. ... QC Specialist III Microbiology Req ID #: 222403 Location:...workstreams that includes but not limited to the QCM Training program, Laboratory Equipment Lifecycle, EM Data Trending, and/or… more
    Charles River Laboratories (04/10/24)
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