• GMP Document Control

    ManpowerGroup (Rockville, MD)
    Our client, a leader in the pharmaceutical industry, is seeking a Pharma Document Control Associate to join their team. The ideal candidate will have strong ... will align successfully in the organization. **Job Title:** Pharma Document Control Associate **Location:** Rockville, MD **Pay...per respective SOP. + Archive and maintain GLP and GMP documents with an accurate inventory, both on and… more
    ManpowerGroup (03/04/25)
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  • Document Control Specialist, Quality…

    Catalent Pharma Solutions (Chelsea, MA)
    …who is responsible for the management and organization of Good Manufacturing Practice ( GMP ) documents. The Document Control Specialist will support the ... ** Document Control Specialist - Quality Assurance** **Position Summary:** Catalent, Inc. is a leading global contract development and manufacturing organization… more
    Catalent Pharma Solutions (04/05/25)
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  • Document Control Specialist

    Astrix Technology (Indianapolis, IN)
    …High School Diploma required + Minimum of 4 years of experience with QA in a GMP environment with Document Control + eQMS experience required (will be ... ** Document Control Specialist** Quality Assurance Indianapolis, IN, US Pay Rate Low: 26.42 | Pay Rate High: 31.25 + Added - 21/03/2025 Apply for Job _Our client… more
    Astrix Technology (03/22/25)
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  • Quality Inspector

    Aerotek (Allendale, NJ)
    …a medical device, nutraceutical, or pharmaceutical production environment + Experience with packaging, GMP , document control , labeling, and inspection + Good ... and packaged products. The ideal candidate will have experience in a GMP environment and will maintain adequate inventory of manufacturing supplies, requisitioning… more
    Aerotek (04/28/25)
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  • Quality Specialist

    Actalent (Germantown, WI)
    …clean workspace. Essential Skills + Quality assurance + Quality control + GMP + Audit + Document control + Food safety + FDA + HACCP + Biology Additional ... documentation practices. The ideal candidate will have experience in quality control and assurance, along with excellent analytical skills. Responsibilities +… more
    Actalent (04/18/25)
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  • Senior Verification GMP Auditor ( Remote)

    The US Pharmacopeial Convention (USP) (Rockville, MD)
    …to individuals with disabilities. **Brief Job Overview** This **Senior Verification GMP Auditor** is a non-supervisory position and hands-on, technical position ... responsible for conducting onsite Good Manufacturing Practice ( GMP ) facility audits and reviewing ingredient and dietary supplement quality control manufacturing… more
    The US Pharmacopeial Convention (USP) (04/08/25)
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  • Senior Scientist - Stability Testing, GMP

    ThermoFisher Scientific (Boston, MA)
    …(Mon-Fri) **Environmental Conditions** Adherence to all Good Manufacturing Practices ( GMP ) Safety Standards **Job Description** At Thermo Fisher Scientific, you'll ... cell banks, critical intermediates, Drug Substance and Drug Product for clinical GMP stability programs of cell and genetic therapies while ensuring compliance with… more
    ThermoFisher Scientific (04/11/25)
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  • Sr. Facilities Technician ( GMP )

    Mentor Technical Group (College Station, TX)
    …which may include Heating Ventilation and Air Conditioning (HVAC), electronic control systems, electrical, compressed air and gases, Reverse Osmosis (RO), wastewater ... Balances/scales, flow, temperature, conductivity, pressure, among others in a GMP /GXP environment. + Perform corrective and preventative maintenance of equipment… more
    Mentor Technical Group (04/23/25)
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  • Manager, QA Document Control

    Catalent Pharma Solutions (Harmans, MD)
    …are met and leading continuous improvement initiatives. The Document Control function supports both the GMP and development operations. Catalent, ... support Phase I/II/III/commercial operations. + Manages document control processes and systems for GMP activities...document control processes and systems for GMP activities in compliance with internal procedures and policies,… more
    Catalent Pharma Solutions (04/29/25)
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  • QA Associate I, Document Control

    Actalent (Hunt Valley, MD)
    …QA Associate I, Document ControlJob Description The QA Associate I, Document Control ensures compliance with cGMP and internal policies, procedures, and ... area. These may include quality operational tasks, product release, process quality, document control , quality systems or operations, or compliance. + Support… more
    Actalent (04/26/25)
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