- Novo Nordisk Inc. (West Lebanon, IN)
- …Provides consistent direction and ensures timely completion of deviation investigations to ensure ongoing consistency for investigation reports that will ... merit and completeness according to regulatory expectations. The Deviation Investigator- Writer will be responsible for initiating investigations and writing… more
- Exela Pharma Sciences, LLC (Lenoir, NC)
- Position Summary:The Investigation Writer , Deviations is responsible for the initiation, investigation , and writing of assigned deviations and associated ... perform Root Cause Analysis to determine the most likely cause of the deviation and identify corrective and preventive actions to reduce deviation recurrence.… more
- Aequor (Libertyville, IL)
- …following: Relevant experience in drug product biopharmaceutical or equivalent industry Investigation Deviation writing cGMP/cGDP Strong scientific and technical ... years relevant experience in drug product biopharmaceutical or equivalent industry Deviation writing cGMP/cGDP Ability to prioritize multiple investigations in… more
- Cynet Systems Inc. (Libertyville, IL)
- …years relevant experience in drug product biopharmaceutical or equivalent industry. Deviation writing. cGMP/cGDP. Ability to prioritize multiple investigations ... The MSAT Tech Writer : Compiles and interprets manufacturing process data to...cell biology concepts & applies them to root cause investigations . Works independently and with Process Engineer(s) to understand… more
- Novo Nordisk (West Lebanon, NH)
- …+ Provides consistent direction and ensures timely completion of deviation investigations to ensure ongoing consistency for investigation reports that will ... merit and completeness according to regulatory expectations. The Deviation Investigator- Writer will be responsible for initiating investigations and writing… more
- ManpowerGroup (Cambridge, MA)
- **Pharmaceutical Deviation and Investigations Writer ** Our client in **Cambridge, MA, Kendall Square** is looking for hardworking, motivated talent to join ... to Friday (9hr/day) 08 AM to 05 PM** **Job Description:** The Senior Deviation / Investigation Writer is responsible for performing **GxP** investigation… more
- Endo International (Rochester, MI)
- …experience in Quality Management Systems such as change management, deviation investigation , and CAPA. The Operations Support Technical Writer will be ... to join our team. **Job Description Summary** The Operations Support Technical Writer , with support of Site Leadership, sponsors a quality and compliance focused… more
- System One (Libertyville, IL)
- …+ Works with GMP Quality Systems to deliver completed Root Cause Analysis investigation reports + Facilitates deviation closure through working with quality ... Job Title: Technical writer Location: Libertyville, IL (Hybrid) Type: Contract Responsibilities...cell biology concepts & applies them to root cause investigations + Works independently and with Process Engineer(s) to… more
- Kelly Services (Libertyville, IL)
- …following: + Relevant experience in drug product biopharmaceutical or equivalent industry + Investigation + Deviation writing + cGMP/cGDP + Strong scientific and ... Technical Writer Role: More than 3 years of experience with the… more
- Endo International (Rochester, MI)
- …major responsibilities, and % of time_ Accountability Responsibilities % of Time Investigation Program Management + Develop/Manage the Investigation Program : + ... deep understanding of Quality Management Systems (QMS), including change management, deviation handling, and CAPA processes. + Collaborate with Quality Assurance and… more
- Insight Global (Boston, MA)
- …risk assessments, in GMP environment, leading, writing and reviewing deviations and investigations . Th This person will need to be comfortable managing several ... experience, comfortable managing multiple stakeholder relationships . Strong technical writer with previous experience authoring, reviewing and editing risk… more
