- 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
- 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
- Novo Nordisk (West Lebanon, NH)
- …of quality systems with the ability to manage Change Controls + Support deviation and CAPA investigations and corrective actions + Support of Health ... technical reports, reviews completed quality records, generates quality comment and deviation responses and has ability to provide training support. Prior experience… 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