Our client is in the pharmaceutical industry and in the middle of a large integration project where they are merging two control documentation systems. They are looking for a technical writer that can write, revise and retire procedural documents and SOP’ s.
The technical writer will be responsible for working with process owners and writing procedural documents for their new control documentation system. This person must have hands-on experience writing policies, procedures, records, SOP’ s, WIs and other related documents. They will need to have experience working with GCP procedures as well as Quality Control of documents. Ideally, this person would have experience working in a R&D environment or with R&D documents. This person should have 8 years’ experience in the pharmaceutical industry in technical writing. They must be comfortable working cross functionally with different documents such as QA, QC, Compliance, etc.
- 8+ years Technical Writing
- GCP experience
- R&D Experience
- Write SOP’ s, Work Instructions, Procedural Documents
- Pharmaceutical Experience
Job Type: Contract