• Director of New Product Introduction (NPI)

    Nissha Medical Technologies (Buffalo, NY)
    …of DMRs (Device Master Records) and DHFs (Design History Files). + Regulatory & Quality Compliance: Ensure new product launches meet FDA 21 CFR Part 820 and ... role is critical in managing cross-functional collaboration between customers, engineering, quality , regulatory , procurement, and manufacturing teams to ensure… more
    Nissha Medical Technologies (11/14/25)
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  • Quality Control Chemist

    Actalent (Lancaster, SC)
    …timelines while balancing testing responsibilities. + Stay informed on updates from USP, FDA , and other regulatory bodies to ensure compliance with analytical ... Job Title: Quality Control ChemistJob Description The Quality Control Chemist is a pivotal member of the laboratory team, reporting to Quality Laboratory… more
    Actalent (12/25/25)
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  • Director, Quality & Compliance Training…

    Otsuka America Pharmaceutical Inc. (Albany, NY)
    …and managing cross-functional teams. + Strong understanding of R&D functions and the regulatory landscape (GxP, ICH, FDA , EMA, etc.). + Proven ability to ... The Director, Quality & Compliance Training, is a senior leader...leader within the Learning Center of Excellence under Global Quality . This role is responsible for developing and executing… more
    Otsuka America Pharmaceutical Inc. (12/20/25)
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  • Quality Compliance Specialist (Contract)

    Actalent (Alameda, CA)
    …GxP processes related to managing vendors, partners, and suppliers. * Familiarity with FDA Quality System Regulations and Pharmaceutical guidelines, 21 CFR Part ... * Assist in maintaining and developing standardized templates based on regulatory requirements and procedures. * Conduct follow-up activities with internal… more
    Actalent (12/18/25)
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  • Quality Assurance

    Aerotek (Oceanside, CA)
    **Now Hiring! Quality Assurance Technician** **Job Description** The Quality Assurance Technician ensures compliance with food regulatory requirements, ... detail. + Strong communication skills. + Knowledge of GMP and FDA standards. + 1-2 years of Quality Assurance experience preferred. + 1-2 years of food industry… more
    Aerotek (12/13/25)
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  • Associate Director, Quality Assurance…

    Astrix Technology (Indianapolis, IN)
    …Investigations, CAPAs, SOPs, Change Controls, and protocols/reports. + Contributes in Regulatory / FDA inspections and audits by providing information or obtaining ... **Associate Director, Quality Assurance -Sterile Manufacturing** Manufacturing Indianapolis, IN, US...for a Pharmaceutical leadership role where you can shape quality operations, build strong teams, and influence the direction… more
    Astrix Technology (12/13/25)
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  • Quality Control Supervisor

    Kelly Services (Fort Collins, CO)
    …responsible for the testing and release of pharmaceutical products. **Title** : Quality Control Supervisor **Location** : Ft. Collins, CO (onsite) **Shift** : 2 ... and ensure that all operations and functions (including the laboratory) are in full FDA , cGMP compliance and staff is properly trained. + Utilize senior analysts to… more
    Kelly Services (12/12/25)
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  • Application Architect - EHS, Quality & PLM…

    IBM (San Francisco, CA)
    …PLM platforms, ERP, and other business applications. . Ensure systems comply with regulatory standards ( FDA , GxP, ISO, OSHA) and internal governance policies. . ... the design, integration, and optimization of enterprise systems across EHS, Quality Management, and Product Lifecycle Management (PLM) domains. This role supports… more
    IBM (12/12/25)
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  • Manager CRS Laboratory

    J&J Family of Companies (Malvern, PA)
    …with all J&J, JSC and government-issued environmental, health, safety, quality and regulatory policies and guidelines, including FDA , EMEA and regulatory ... all local, state and federal regulations and guidelines including FDA , EPA, and OSHA. Complies with all company and...of new and emerging technologies and practices for regulated quality labs. + Experience contributing to regulatory more
    J&J Family of Companies (12/23/25)
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  • Principal Specialist, Validation

    Boehringer Ingelheim (Athens, GA)
    …written and verbal communication skills + Excellence in comprehension/application of FDA /EU/USDA regulatory requirements for production and distribution of ... at the BIAH location from concept through process validation ensuring GxP regulatory compliance continues as outlines in BIAH's Validation Master Plan (MVP) and… more
    Boehringer Ingelheim (12/12/25)
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