Technical Writer, Investigation Deviations

Manpower Engineering

Job Description

Technical Writer

In this Technical Writer, you will possess a strong quality investigation and change control writing background at a sterile liquid pharmaceutical company.

Are you interested? Please contact Alex Hettinger with an updated resume at

The ideal Technical Writer candidate will possess the following experience:

  • Role will require focused expertise in sterile operations, quality and laboratory controls
  • Prepare Manufacturing, Process, Laboratory and complaint investigations including root cause, product impact analysis, and CAPA identification.
  • Perform review and facilitate handling and closure of change control records representing process, product and documentation changes.
  • Strong writing aptitude and ability to review technical documents.
  • Ability to conduct interviews, gather pertinent information, and write investigation reports
  • Work with Laboratory, Maintenance, Engineering and Operations to identify root cause(s) and CAPA actions, as appropriate.

We've got the right opportunity. Tell us why you're the right person. Apply today!

  • Minimum 5 - 7 years' previous experience working in Pharmaceutical Sterile Liquid Manufacturing
  • Minimum 4 - 6 years' experience in investigation writing / CAPA and change controls in the Pharmaceutical industry.

Job Requirements