- 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 three years manufacturing/ technical experience in a regulated GMP environment;… more
- TEKsystems (Indianapolis, IN)
- …requirements, test scripts and traceability (UAT Testing). Position Overview: * Experienced Technical Writer with a focus on system validation, specifically ... Document Management System (DMS). Qualifications: * 3+ years of experience in technical writing within a regulated industry (Pharma, Biotech, Animal Health). *… 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
- ThermoFisher Scientific (Juneau, AK)
- …and in the future. Location/Division Specific Information Our PPD (TM) Laboratory services GMP Lab team has a direct impact on improving patient health through the ... with PPD, Client, eCTD policy and procedure on publications. + Reviews technical documents for accuracy, formatting, consistency and compliance to protocols or SOPs.… 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
- Edwards Lifesciences (Irvine, CA)
- …outcomes and discovering lasting solutions for unmet patient needs. Our Sr. Specialist, Technical Writer position is a unique career opportunity that could be ... Writing role will develop and create accurate Good Manufacturing Practices ( GMP ) technical documents. **How you'll make an impact:** * Provide technical … 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
- 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)
- …**Contact Us** **Email:** hrop_###@bayer.com **Job Segment:** Medical Device, QC, Technical Writer , Healthcare, Entry Level, Quality, Technology, Manufacturing ... manner; * Knowledge of statistical process control (SPC), good manufacturing practices ( GMP ), traceability and material review board (MRB); * Ability to work… more
- Bayer (Pittsburgh, PA)
- …841547 **Contact Us** **Email:** hrop_###@bayer.com **Job Segment:** Medical Device, QC, Technical Writer , Industrial, Healthcare, Quality, Technology, ... your knowledge of statistical process control (SPC), good manufacturing practices ( GMP ), traceability and material review board (MRB) while working independently… more