• DivIHN Integration Inc (Atlanta, GA)
    …Talent Specialist: Divya at 224 369 2969 Sivanesan at 224 369 0756 Title: Technical Writer 3 (REMOTE) Location: Remote Duration: 1.1 Years Description: We are ... looking for a Technical Writer to produce high-quality documentation that...JavaScript) is a plus Experience: Medical Devices Drug Discovery Pharmaceutical Regulated Healthcare Industry experience is a plus Education… more
    JobGet (09/15/24)
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  • Technical Writer

    Kelly Services (Lenwood, CA)
    **Job Title:** Technical Writer ( Pharmaceutical Industry) - Remote (Temporary, 6+ months) **About the Role:** Are you passionate about translating complex ... information into clear, concise documentation? We're seeking a skilled Technical Writer to join our team in...detail-oriented writer with a strong grasp of technical language, particularly in the medical and pharmaceutical more
    Kelly Services (09/05/24)
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  • USA Technical Writer I Manufacturing…

    Adecco US, Inc. (Pearl River, NY)
    Adecco Healthcare & Life Sciences is hiring a remote contract Technical Writer for our Pharmaceutical partner. The anticipated wage for this position is ... criteria 1st Shift: Responsible for designing, developing, and updating required technical documentation. Responsible for technical writing/editing for all types… more
    Adecco US, Inc. (09/11/24)
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  • Technical Writer

    Kelly Services (Cincinnati, OH)
    Kelly Science has an immediate opening for a Technical Writer for our growing client near West Chester, OH. Join us in shaping the future of technical ... documentation and making a meaningful impact every day! **Title** : Technical Writer **Location** : Cincinnati, OH (hybrid, 3 days in-office weekly) **Length** :… more
    Kelly Services (09/13/24)
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  • QA Compliance Technical Writer

    Integra LifeSciences (Princeton, NJ)
    …what's possible and making headway to help improve outcomes. The Quality Compliance Technical Writer will work with Quality system leadership and cross ... documentation and responses in support of regulatory compliance correspondence. The Quality Compliance Technical Writer will serve as primary writer for… more
    Integra LifeSciences (09/12/24)
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  • Senior Proposal Writer Manager

    The US Pharmacopeial Convention (USP) (Rockville, MD)
    …strengthens health systems at local, regional, and global levels to deliver end-to-end pharmaceutical services. The Senior Proposal Writer Manager will serve as ... disabilities. Brief Job Overview USP seeks a Senior Proposal Writer Manager to serve as a key member of...capability statements and other stock language describing USP's core technical areas (eg, local pharmaceutical manufacturing; medicines… more
    The US Pharmacopeial Convention (USP) (08/28/24)
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  • Technical Writer I - Manufacturing…

    Catalent Pharma Solutions (Madison, WI)
    ** Technical Writer I - Manufacturing Sciences & Technology** **Postion Summary** Catalent is a global, high-growth, public company and a leading partner for the ... pharmaceutical industry in the development and manufacturing of new...Line Development, Process Development, Analytical Development, and Manufacturing. This Technical Writer I, Manufacturing Sciences & Technology… more
    Catalent Pharma Solutions (08/16/24)
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  • Technical Writer I

    ThermoFisher Scientific (St. Louis, MO)
    …**Job Description** **How will you make an impact?** + We are searching for a Technical Writer I with a good background in scientific writing. This member of ... that supports the manufacture of life-saving clinical and commercial drug products. The technical writer I will use standard batch record templates and… more
    ThermoFisher Scientific (08/24/24)
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  • Deviation Investigator - Writer (Biotech…

    Novo Nordisk (West Lebanon, NH)
    …+ Experience in a cGMP environment (eg Production, Development, Process Engineering, Technical Services or related field) in pharmaceutical / biotech industry + ... + 12 weeks Paid Parental Leave + Free access to Novo Nordisk-marketed pharmaceutical products At Novo Nordisk, you will find opportunities, resources and mentorship… more
    Novo Nordisk (09/05/24)
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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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  • Associate Lead I - Biomanufacturing, Compliance,…

    Catalent Pharma Solutions (Madison, WI)
    **Position Summary** **Associate Lead I - Biomanufacturing, Technical Writing** Catalent is a global, high-growth, public company and a leading partner for the ... pharmaceutical industry in the development and manufacturing of new...and client requirements. The Associate Lead I - Biomanufacturing, Technical Writing under minimal supervision, authors and revises deviation… more
    Catalent Pharma Solutions (08/01/24)
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  • Technical Writer (Onsite)

    Novo Nordisk (West Lebanon, NH)
    …+ 12 weeks Paid Parental Leave + Free access to Novo Nordisk-marketed pharmaceutical products At Novo Nordisk, you will find opportunities, resources and mentorship ... in local change control process to support revision of standards. Interfaces with technical writers at other sites & in Manufacturing Development. This could be a… more
    Novo Nordisk (09/05/24)
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  • Associate Principal Medical Writer (Hybrid)

    Merck (Boston, MA)
    **Job Description** The Associate Principal Medical Writer is responsible for leading medical writing deliverables that support the Translational Medicine clinical ... writing portfolio. **The Associate Principal Medical Writer :** + Independently leads and authors clinical regulatory documents (eg, protocols, pivotal clinical study… more
    Merck (08/28/24)
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  • Sr Technical Writer

    MD Anderson Cancer Center (Houston, TX)
    Provides technical writing and editing of grants, publications, clinical research proposals, and clinical trial protocols. Impacts the visibility of melanoma ... projects concurrently and, through excellent communication skills, deliver high-quality technical content for both internal and external publication. 2. Demonstrated… more
    MD Anderson Cancer Center (09/07/24)
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  • Business Development/Proposal Writer

    The US Pharmacopeial Convention (USP) (Rockville, MD)
    …check prior to submission. + Provides ad hoc research, and in coordination with technical and other proposal team leads as required. + Mentors junior staff on ... standards and managing compliant and responsive proposals. + Engage with staff technical experts to become familiar with the subject matter. + Research, monitor,… more
    The US Pharmacopeial Convention (USP) (07/04/24)
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  • Sr. Medical Writing Specialist

    ManpowerGroup (Deerfield, IL)
    Our client in pharmaceutical Industry is seeking a Sr Medical Writer to join their team. The ideal candidate will have experience in scientific or clinical ... which will align successfully in the organization. **Job Title: Senior Medical Writer ** **Location: Fully Remote** **Pay Range: $70/hr - $78/hr** **What's the Job?**… more
    ManpowerGroup (09/05/24)
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  • Technology Manager

    Publicis Groupe (New York, NY)
    …consumer and professional marketing, strategic consulting, and medical education to pharmaceutical and wellness brands. Our mission is to inspire a healthier, ... planet with very caring, very resourceful people. So, if you're a rockstar writer , aspiring strategist, jill-or jack-of all trades, or just an all-around nice… more
    Publicis Groupe (08/22/24)
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  • Regulatory Operations Manager - Multiple Positions…

    Publicis Groupe (New York, NY)
    …consumer and professional marketing, strategic consulting, and medical education to pharmaceutical and wellness brands. Our mission is to inspire a healthier, ... planet with very caring, very resourceful people. So, if you're a rockstar writer , aspiring strategist, jill-or jack-of all trades, or just an all-around nice… more
    Publicis Groupe (08/09/24)
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  • Associate Director - CMC Regulatory

    Lilly (Philadelphia, PA)
    …with 5+ years of CMC regulatory experience or related experience (eg CMC writer ). **Additional Skills/Preferences:** + Excellent technical writing skills + PET ... manufacturing and analytical procedures and method validations + Review technical documents including testing protocols, technical reports, and… more
    Lilly (08/24/24)
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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 ... Seaport district of Boston supporting one of our top pharmaceutical clients. This is a first shift role, on-site...through Friday. This position will be supporting the growing technical services team in their risk assessment efforts. This… more
    Insight Global (08/06/24)
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