- Actalent (Parsippany, NJ)
- …Specialist - Technical WriterJob Description We are looking for a Compliance Specialist - Technical Writer who will play a crucial role in writing ... and completing investigations and deviations from a compliance and operations standpoint. The ideal candidate will conduct...the full life cycle of investigations, and engage in technical writing. This role requires strong communication skills as… more
- Actalent (Parsippany, NJ)
- … Compliance Specialist - Technical WriterJob Description We are seeking a Compliance Specialist - Technical Writer to join our team. The role ... involves writing and completing investigations and deviations from a compliance and operations perspective. You will be responsible for reviewing investigations and… more
- Integra LifeSciences (Boston, MA)
- …patient outcomes and set new standards of care. The Senior Quality Compliance Specialist - Technical Writer will work with Boston quality system ... cross-functional stakeholders including quality, manufacturing and engineering on communicating technical information. + Develop, write, edit and revise policies,… more
- Colorado State University (Fort Collins, CO)
- Posting Detail Information Working TitleCultural Resources Planning Specialist , Technical Writer - Fort Collins, CO Position LocationFort Collins, CO Work ... restaurants, gardens, and more. Position Summary CEMML is hiring a Cultural Resources Planning Specialist ( Technical Writer ). The Technical Writer … more
- Indigo IT, LLC (Ashburn, VA)
- Technical Writer /Reporting Specialist Ashburn, VA Remote SUMMARY: Founded in 2001, Indigo IT is an award winning information technology consulting and ... integral member of the CBP End User Device IT Management Services team, the Technical Reporting Specialist will be responsible for technical writing,… more
- System One (Harmans, MD)
- Title: Technical Writer - Manufacturing Specialist Pay Rate: $21/hr Location: Harmons MD Schedule: Monday through Friday 8-5 onsite Duration: 12 months ... technical competency in biopharmaceutical manufacturing processing in a GMP compliance environment (eg Production, Development, Process Engineering, Technical … more
- Adecco US, Inc. (Harmans, MD)
- …with a passion for biopharmaceutical manufacturing? Join our team as a **Manufacturing Technical Specialist ** , where you'll play a critical role in ensuring ... executing root cause investigations, and managing GMP documentation to ensure compliance and efficiency. **What You'll Do:** ✔️ Lead and conduct **deviation… more
- Actalent (Tamarac, FL)
- Document Control Specialist The Specialist - Global Quality & Compliance will create, revise, and manage global quality documentation, including SOPs, ... Policy. This role supports global and site quality initiatives, ensuring compliance with regulatory standards and internal requirements. Responsibilities + Author… more
- Fujifilm (Santa Ana, CA)
- **Position Overview** We are hiring a Clinical Affairs Specialist . The Clinical Affairs Specialist will be responsible for assisting in the development and ... devices and in vitro diagnostic devices. In addition, the Clinical Affairs Specialist will assist in performing annual activities associated with Post Market… more
- ManpowerGroup (Princeton, NJ)
- …easy access and updates. **Qualifications:** **Experience:** + Proven experience as a Content Writer , Procedure Writer , or RFP/Proposal Specialist . + Strong ... **Contract Length:** 6 months **Job Summary:** We are seeking an experienced Content Writer with expertise in RFP/Proposal Management to join our team. This role… more