- Catalent Pharma Solutions (Philadelphia, PA)
- ** Technical Investigation Writer ** **Position Summary:** Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose ... Catalent Pharma Solutions in Philadelphia, PA is hiring a Technical Investigations Writer . The Technical ...assurance experience is preferred + At least five years manufacturing/ technical experience in a regulated GMP environment;… more
- Catalent Pharma Solutions (Greenville, NC)
- ** Technical Writer ** **Position Summary** Catalent's Greenville, NC facility specializes in end-to-end turn-key solutions for oral solid dosage forms, including ... and to the safety of every patient, consumer and Catalent employee. The Technical Writer is responsible for collecting, organizing, formatting and authoring … more
- Actalent (Parsippany, NJ)
- Job Title: Technical WriterJob Description We are seeking an experienced Technical Writer to manage and complete investigations and deviations in compliance ... with GMP and manufacturing standards. The ideal candidate will have strong technical writing skills, excellent communication abilities, and experience in root… 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 Start: ... technical competency in biopharmaceutical manufacturing processing in a GMP compliance environment (eg Production, Development, Process Engineering, Technical… more
- Lilly (Lebanon, IN)
- …build the processes and facility to enable a successful startup into GMP manufacturing operations. **Position Brand Description:** The Health Safety and Environment ... (HSE) Permit Writer will develop and maintain safe work permits within...the necessary systems and business processes required to support GMP operations, and build the site culture. This will… 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 the ... by driving continuous improvement, executing root cause investigations, and managing GMP documentation to ensure compliance and efficiency. **What You'll Do:** ✔️… more
- 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
- 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
- ManpowerGroup (Severn, MD)
- …one of the Largest multinational Company in the US is looking for a Technical Writer - Manufacturing Specialist in Severn MD 21077 United States location. ... JOB TITLE: Technical Writer - Manufacturing Specialist LOCATION: Severn...technical competency in biopharmaceutical manufacturing processing in a GMP compliance environment (eg Production, Development, Process Engineering, … more
- Amneal Pharmaceuticals (Piscataway, NJ)
- …as per GMP guidelines and SOP procedures + Work closely with Technical Writer in generating detailed equipment SOP's, focusing on set-up, operation, and ... compliance. + Responsible for 100% documentation accuracy on all GMP documents, such as bath records, log books, training...a "Train the Trainer" program, working closely with the Technical Writer in generating new and detailed… more
- Kelly Services (Morris Plains, NJ)
- …Compliance Specialist will lead laboratory investigations (including OOS/OOT), author technical protocols and reports, perform data reviews, conduct trend analysis, ... compliance initiatives. The Specialist will serve as the lead investigator and writer for lab-related issues, ensuring all compliance tasks and investigations are… more
- 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
- Bayer (Pittsburgh, PA)
- …Code:** 838995 **Contact Us** **Email:** hrop_###@bayer.com **Job Segment:** QC, Technical Writer , Medical Device, Quality, Technology, Healthcare, Manufacturing ... your knowledge of statistical process control (SPC), good manufacturing practices ( GMP ), traceability and material review board (MRB) while working independently… more
- Actalent (Parsippany, NJ)
- …QC laboratory. The successful candidate will conduct laboratory investigations, author technical protocols and reports, perform data review and trend analysis, and ... Identification, Sterility Testing, LIMS). + Serve as Lead investigator and writer for lab-related issues, conduct formal investigations, and ensure timely completion… more