- Novo Nordisk Inc. (West Lebanon, IN)
- …your career. Are you ready to realize your potential? The PositionThe Deviation Investigator- Writer is responsible for investigating and writing of deviations ... the technical merit and completeness according to regulatory expectations. The Deviation Investigator- Writer will be responsible for initiating investigations… more
- Actalent (Clayton, NC)
- Job Title: Deviation Writer Job Description A Global Pharmaceutical Manufacturer is seeking a Quality Investigator for Aseptic Production Investigations. The ... individual will perform investigations specifically pertaining to the Aseptic Core and its processes. Responsibilities include conducting historical searches, reviewing videos, interviewing colleagues, and reviewing supporting documentation (batch records,… more
- Novo Nordisk (West Lebanon, NH)
- …your career. Are you ready to realize your potential? The Position The Deviation Investigator- Writer is responsible for investigating and writing of deviations ... the technical merit and completeness according to regulatory expectations. The Deviation Investigator- Writer will be responsible for initiating investigations… 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 ... to Friday (multiple shifts available )** **Job Description:** The Senior Deviation /Investigation Writer is responsible for performing GxP investigation… more
- Insight Global (Elkhorn, NE)
- Job Description Insight Global is seeking a Technical Writer in Omaha, Nebraska. This person will be primarily responsible review and updating existing SOPs to ... (Or Bio production, GMP) Knowledge or previous experience with change management and deviation management from a quality perspective null We are a company committed… more
- Cambrex High Point (Charles City, IA)
- …where You Matter by applying today! Job Overview The PE Technical Writer will be responsible for consistently generating high quality technical documents, such ... process validation protocols and reports, WINS and SOPs, campaign reports, investigation/ deviation reports and other documents needed to support Operations while… more
- Catalent Pharma Solutions (Madison, WI)
- …I - Biomanufacturing, Technical Writing under minimal supervision, authors and revises deviation records, preventative actions, and other related cGMP documents in a ... timely manner. Position is 1st shift M-F 8AM-5PM and is 100% on site at Madison, WI facility. Catalent is committed to a Patient First culture through excellence in quality and compliance, and to the safety of every patient, consumer, and Catalent employee.… more
- Bristol Myers Squibb (Summit, NJ)
- …closure of Change Controls Actions. **Continuous Improvement** + Human avoidable deviation reduction driven with continuous improvement. **Required for all job ... functions** + Demonstrated ability to collaborate with Manufacturing Operations, QA, MS&T, and other groups to verify the correct reviewers/approvers are selected. + Ensuring on time review/approval/effectiveness. + Other duties may be assigned, as necessary.… more
- Bristol Myers Squibb (Summit, NJ)
- …Therapy team. The Sr. Specialist role is a combined role working 50% Technical Writer role and 50% Specialist role within the QA Shop floor Department that provides ... quality oversight in the manufacturing areas of S12. Tech Writer role works independently and is responsible for authoring high-quality documentation in support of… more
- Butler America (Grand Prairie, TX)
- …He/she supervises, in a project organization, System Lead, Mechanical Lead and Technical Writer in order to ensure the action items are delivered on time, on ... daily basis, the project team (system, mechanic and tech writer ). - Ensure the scope of deliverables is well...Project Engineer and Chief Engineer. Alert in case of deviation and proactively propose and implement corrective actions. -… more
- Johnson Controls (Milwaukie, OR)
- …the plan. Identifies actions required to be taken in the event of deviation from the plan. Adheres to Johnson Controls standardized procedures and processes. ... computer working capabilities in MS Office (excel, word, power point), Adobe Writer , Visio and basic Windows environment. Preferred + Master's degree. +… more
- Insight Global (Boston, MA)
- …experience, comfortable managing multiple stakeholder relationships . Strong technical writer with previous experience authoring, reviewing and editing risk ... assessment, CAPA and deviation documents . Effective communicator with ability to influence a group of people . Previous experience with an eQMS system, ideally… more
