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Medical Writer
PSG Global Solutions · Chesterfield, MO, United States
About The Role
The BRD organization within the Pharm Sci BTx organization needs to hire a technical writer. This colleague will perform the following activities:
- Assist with verification of data within regulatory documents or reports.
- Support the bioprocess R&D (BRD) teams in tracking document completion, data verification strategies and completion of edits.
- Create drafts of new technical or regulatory documents using existing examples, templates or reports
- Assist Bioprocess team authors in assembling, formatting, and proofreading figures, tables and content.
SKILLS
- Excellent oral and written communications with experience in technical writing of reports and/or regulatory documents
- Regulatory, GMP or Pharmaceutical experience, preferrably in bioprocess or cell line development areas is desirable
- Detail oriented
EXPERIENCE
- 3-5 years
EDUCATION
- Scientific Background; BS or higher Biology, Chemistry, Biochemistry, Molecular Biology, Engineering, or similar
- All your information will be kept confidential according to EEO guidelines.
- IF THIS IS THE JOB OPPORTUNITY FOR YOU GIVE ME A CALL AT 646-618-8925 ASAP!
- I want to know more about your preferences. If in case you know someone who might be interested for this, feel free to pass it along. I look forward to hearing from you!
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