• Pharma Technical Writer

    System One (New Brunswick, NJ)
    Job Title: Pharma Technical Writer Location: New Brunswick, NJ Hours/Schedule: Mon-Friday (normal business hours) Compensation: $34.87- $44.29 Type: Contract ... Overview Leading pharmaceutical company looking for an experienced Technical Writer . Ideal candidates should have at...ready standards for final publication. + Experience in bio tech/ pharma e2e product development required. Must be capable of… more
    System One (09/23/25)
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  • Technical Writer

    Kelly Services (North Charleston, SC)
    ** Technical Writer - 6-Month Contract (Fully... technical field required + 3+ years of technical writing experience in biotech, pharma , or ... $35-$45/hour **Type:** 6-Month Contract (Fully Benefited) We are seeking a ** Technical Writer ** for a fully onsite, 6-month contract position with full benefits.… more
    Kelly Services (09/30/25)
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  • QA Investigator/ Technical Writer

    Actalent (Allendale, NJ)
    …WriterJob Description We are seeking a dedicated Investigation and Deviation Writer responsible for writing and completing investigations and deviations from a ... GMP operations and/or Quality Assurance in Cell Therapies, Biotechnology, or Bio- Pharma . + Familiarity with e-Quality Management Systems. Additional Skills &… more
    Actalent (10/07/25)
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  • Technical Writer Specialist

    Mentor Technical Group (PR)
    Mentor Technical Group (MTG) provides a comprehensive portfolio of technical support and solutions for the FDA-regulated industry. As a world leader in life ... science engineering and technical solutions, MTG has the knowledge and experience to...field. + Experience: 2-5 years in a regulated industry ( pharma , biotech, medical devices) with direct experience in SOP… more
    Mentor Technical Group (08/03/25)
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  • QC Scientist ( pharma /micro)

    Astrix Technology (Wilmington, OH)
    …+ Good verbal and written communication skills; confident presenter, clear, concise technical writer . + Familiar with common MS Office software packages. ... **QC Scientist ( pharma /micro)** Quality Control Wilmington, OH, US Pay Rate...as CMC Team support. + Write documents (SOPs, specifications, technical reports) + Execute, oversee instrument qualification as necessary.… more
    Astrix Technology (08/15/25)
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  • QMS Document Manager

    Roche (South San Francisco, CA)
    …global QMS documents. This role involves working directly with members of the Pharma Technical Network, including QMS Process Owners, document authors, Subject ... writing standards are followed, as required, in conjunction with the QMS technical writer . + You will maintain effective working relationships with local and… more
    Roche (10/04/25)
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