• Quality Specialist / Technical Writer

    Teledyne (Billerica, MA)
    …development, oceanographic research, deepwater oil and gas exploration and production, medical imaging and pharmaceutical research.​ We are looking for individuals ... opportunities. \#TeledyneFLIRDefenseJobs **Job Summary:** The Quality Specialist / Technical Writer will manage Quality documentation, including Standard Operating Procedures… more
    Teledyne (06/07/25)
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  • Associate Customs Entry Writer (weekend…

    CH Robinson (Laredo, TX)
    CH Robinson is seeking an **Associate Customs Entry Writer ** to join our Global Forwarding division. As a key player on our customs team, you'll navigate the ... the art of precise data management, and deepen your regulatory knowledge. If you are organized, possess exceptional communication...benefits that matter to you most, including: + Two medical plans (including a High Deductible Health Plan) +… more
    CH Robinson (07/23/25)
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  • Customs Entry Writer

    CH Robinson (Southfield, MI)
    …the world's largest logistics platforms and we're looking for our next **Customs Entry Writer ** . Is that you? You'll be responsible for the accurate and timely ... expert in our systems and processes and provide on-going regulatory training. Many of our successful Customs Entry Writers...benefits that matter to you most, including: + Two medical plans (including a High Deductible Health Plan) +… more
    CH Robinson (08/02/25)
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  • Senior Customs Entry Writer

    CH Robinson (Atlanta, GA)
    CH Robinson is seeking a Senior Customs Entry Writer for our office in Atlanta. In this role, you'll be recognized as role model for account management excellence ... and seizing opportunities to demonstrate their professionalism--thorough knowledge of regulatory requirements and supply chains, and ability to create meaningful… more
    CH Robinson (08/01/25)
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  • Content Writer

    Robert Half The Creative Group (Boston, MA)
    Description We are seeking a creative and versatile Content Writer to create compelling marketing content that effectively communicates complex investment concepts ... for diverse formats and channels, including digital marketing. . Knowledge of regulatory requirements in the investment industry. . Familiarity with communicating to… more
    Robert Half The Creative Group (07/29/25)
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  • Procedure Writer

    Actalent (Wilmington, NC)
    Procedure Writer Job Description We are seeking a detail-oriented and process-driven individual to join our team as a Procedure Development and Implementation ... Visio). + Familiarity with quality management systems (QMS) or regulatory standards (eg, ISO, FDA, HIPAA) is a plus....for this temporary role may include the following: * Medical , dental & vision * Critical Illness, Accident, and… more
    Actalent (07/23/25)
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  • Customs Entry Writer

    Kuehne+Nagel (Mendota Heights, MN)
    …such as ensuring the timely and seamless transport of hearing aids and advanced medical devices that change lives. At Kuehne+Nagel, our work contributes to more than ... we imagine. **‎** You as Customs Entry Writer will communicate with customers, freight forwarders, and other...and ocean ports along with basic knowledge of US Regulatory Laws + Basic knowledge of INCO terms, the… more
    Kuehne+Nagel (06/27/25)
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  • Technical Communications Specialist - Technical…

    Actalent (Minneapolis, MN)
    …Adobe Photoshop, and document management systems is a plus. + Knowledge of regulatory affairs and medical device labeling. + Graphic design and editing ... accuracy and compliance with global regulations. + Collaborate with engineering, regulatory , quality, and product development teams to extract necessary information… more
    Actalent (08/02/25)
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  • Scientific Writer

    University of Miami (Miami, FL)
    …Summarizes data from clinical studies for submission to appropriate governmental/ regulatory agencies. Edits all extramurally funded proposals for grammar, ... analysis, assisting in the preparation of scientific manuscripts, presentations, and regulatory submissions. This list of duties and responsibilities is not intended… more
    University of Miami (05/18/25)
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  • Technical Writer Specialist

    Mentor Technical Group (PR)
    …knowledge and experience to ensure compliance with pharmaceutical, biotechnology, and medical device safety and efficacy guidelines. With offices in Caguas, Puerto ... revise, and maintain SOPs and related controlled documents in accordance with regulatory and company standards. + Collaborate with cross-functional teams (eg, QA,… more
    Mentor Technical Group (08/03/25)
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