• Technical Writer ( GMP )

    Kelly Services (Oklahoma City, OK)
    …seeking an experienced Manufacturing Tech Writer with a strong background in GMP environments and technical transfer. The ideal candidate will be responsible ... **Tech** **nical** ** Writer ( GMP )** **Batch Record Review &...process documentation from scratch. + Review, revise, and maintain technical documents to ensure they meet current GMP more
    Kelly Services (10/09/24)
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  • Technical Writer

    Randstad US (Largo, FL)
    technical writer . + largo , florida + posted october 24, 2024 **job details** summary + $33 per hour + contract + bachelor degree + category life, physical, and ... in the World and we are sourcing for a Technical Writer in the Tampa Bay, FL...(Good Laboratory Practice), Data Validation Plan, Regulatory Briefing Documents, GMP (Good Manufacturing Practice) Equal Opportunity Employer: Race, Color,… more
    Randstad US (11/13/24)
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  • Technical Writer

    Actalent (Hillsboro, OR)
    Job Title: Technical Writer Job Description Discover Impactful Work: You will be working in manufacturing, partnering with engineering and quality management to ... to discuss progress and strategic goals. Essential Skills + Technical writing + Document control + Quality assurance +...Quality control analysis + Document review + Understanding of GMP and audit requirements Additional Skills & Qualifications +… more
    Actalent (11/02/24)
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  • Document Control/ Technical Writer

    Actalent (Irvine, CA)
    Technical Writer - Process Improvement Job Description + We are seeking a detail-oriented contractor to develop new and/or revise existing documentation to ... operational processes. + The ideal candidate has experience in technical writing, process improvement, and documentation standards. Responsibilities + Document… more
    Actalent (11/05/24)
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  • Manufacturing Deviation and Investigations…

    ManpowerGroup (Cambridge, MA)
    **Pharmaceutical Deviation and Investigations Writer ** Our client in **Cambridge, MA, Kendall Square** is looking for hardworking, motivated talent to join their ... (multiple shifts available )** **Job Description:** The Senior Deviation/Investigation Writer is responsible for performing GxP investigation activities and owning… more
    ManpowerGroup (09/11/24)
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  • Technical Writer /Lead Investigator

    ThermoFisher Scientific (Mount Prospect, IL)
    …Standard (Mon-Fri) **Environmental Conditions** Adherence to all Good Manufacturing Practices ( GMP ) Safety Standards, Office, Some degree of PPE (Personal Protective ... industry. + Minimum of 3 years of experience in technical or scientific writing principles. + Demonstrable knowledge of...to mentor and train others. + Experience with training technical writing skills and Root Cause Analysis Tools preferred.… more
    ThermoFisher Scientific (11/10/24)
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  • Regulatory, Clinical, and Technical

    Alaka'ina Foundation Family of Companies (Frederick, MD)
    …Clinical Data Manager/Regulatory Writer ; Quality Assurance Officer; Regulatory Scientist; Technical Writer ; Program Manager; Biomedical Science Writer ; ... Regulatory, Clinical, and Technical Clinical Trial support Location MD - Frederick...Practices (GCP) Good Laboratory Practices (GLP), Good Manufacturing Practice ( GMP ), or related guidelines is preferred. REQUIRED CITIZENSHIP AND… more
    Alaka'ina Foundation Family of Companies (10/29/24)
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  • QC Analytical Investigator

    Insight Global (Boston, MA)
    …management experience, comfortable managing multiple stakeholder relationships . Strong technical writer with previous experience authoring, reviewing and ... role, on-site Monday through Friday. This position will be supporting the growing technical services team in their risk assessment efforts. This role will be… more
    Insight Global (11/05/24)
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  • Senior Manufacturing Quality Engineer

    Grifols Shared Services North America, Inc (San Diego, CA)
    …independently writing SOPs, forms, and risk assessments. Must be a strong technical writer . + Excellent presentation skills, including independently preparing, ... the Operations and Quality departments. + Independently write complex technical documentation such change controls, protocols, test plans, quality specifications… more
    Grifols Shared Services North America, Inc (10/09/24)
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  • QC Microbiologist

    Actalent (Parsippany, NJ)
    …for the QC laboratory. This includes conducting laboratory investigations, authoring technical protocols and reports, performing data reviews and trend analyses, ... on-call, and holidays as needed. + Serve as Lead investigator and writer for lab-related issues, conduct formal investigations, and ensure lab investigations are… more
    Actalent (11/07/24)
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