• Jt011 - PD Project Management Specialist

    Quality Consulting Group (Villalba, PR)
    QUALITY CONSULTING GROUP, a leader in the pharmaceutical , biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and ... you'll work with a highly enthusiastic team, contributing in a world-class manufacturing industry in Puerto Rico & USA. Responsibilities: + Oversees and manages… more
    Quality Consulting Group (11/13/25)
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  • Jt960 - Sr. Compliance Specialist

    Quality Consulting Group (Juncos, PR)
    QUALITY CONSULTING GROUP, a leader in the pharmaceutical , biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and ... you'll work with a highly enthusiastic team, contributing in a world-class manufacturing industry in Puerto Rico & USA. Responsibilities: + Develops, implements,… more
    Quality Consulting Group (11/13/25)
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  • Jt730 - Sr Quality Systems Specialist

    Quality Consulting Group (Juncos, PR)
    QUALITY CONSULTING GROUP, a leader in the pharmaceutical , biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and ... you'll work with a highly enthusiastic team, contributing in a world-class manufacturing industry in Puerto Rico & USA. Responsibilities: + Provides oversight for… more
    Quality Consulting Group (11/07/25)
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  • Quality Assurance Specialist

    Mentor Technical Group (Juncos, PR)
    …MTG has the knowledge and experience to ensure compliance with pharmaceutical , biotechnology, and medical device safety and efficacy guidelines. With offices ... Germany, Canada, and South America. Responsibilities: + Quality Professional with Manufacturing Process Audit and Batch Record Review experience. + Available for… more
    Mentor Technical Group (11/15/25)
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  • QC Specialist

    Genentech (Hillsboro, OR)
    …Technical Operations (HTO) is a drug product & finished goods manufacturing organization responsible for the reliable delivery of Roche's commercial portfolio ... 5-7 years experience working in a cGMP or similarly regulatedenvironment in the pharmaceutical or science industry. 3-5 years experience with a Master's Degree or… more
    Genentech (11/13/25)
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  • Technical Writer Specialist

    Mentor Technical Group (PR)
    …MTG has the knowledge and experience to ensure compliance with pharmaceutical , biotechnology, and medical device safety and efficacy guidelines. With offices ... and company standards. + Collaborate with cross-functional teams (eg, QA, QC, Manufacturing , R&D, Regulatory) to gather process information and ensure SOPs reflect… more
    Mentor Technical Group (11/01/25)
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  • FSP - Sr. Instrument Qualification…

    ThermoFisher Scientific (New Brunswick, NJ)
    …Schedule** Standard (Mon-Fri) **Environmental Conditions** Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Laboratory Setting, Some degree of ... you, the employee, to gain direct experience working onsite at a pharmaceutical / biopharmaceutical company, all while maintaining full-time benefits. This is a fully… more
    ThermoFisher Scientific (10/31/25)
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  • FSP - Lab Support Specialist

    ThermoFisher Scientific (Lawrenceville, NJ)
    …Schedule** Standard (Mon-Fri) **Environmental Conditions** Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Laboratory Setting, Some degree of ... you, the employee, to gain direct experience working onsite at a pharmaceutical / biopharmaceutical company, all while maintaining full-time benefits. This is a fully… more
    ThermoFisher Scientific (10/23/25)
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  • EHS Quality Specialist

    Mentor Technical Group (Carolina, PR)
    …MTG has the knowledge and experience to ensure compliance with pharmaceutical , biotechnology, and medical device safety and efficacy guidelines. With offices ... law or regulation changes that impact the client. + Participate in manufacturing meetings to discuss workplace safety and regulatory concerns and opportunities. +… more
    Mentor Technical Group (10/22/25)
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  • CMMS Specialist (Blue Mountain RAM)

    Mentor Technical Group (West Columbia, SC)
    …MTG has the knowledge and experience to ensure compliance with pharmaceutical , biotechnology, and medical device safety and efficacy guidelines. With offices ... of five (5) years professional experience with research and/or manufacturing laboratory equipment/instrumentation within the regulated industry. + Requires good… more
    Mentor Technical Group (09/26/25)
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