Location: (100% Remote Role)
Pay Rate: Open
Contract: 6 Months w/ Possible Extension
Department: Pharmaceutical Operations & Supply Chain
Experience:
- Possess substantial Chemistry, Manufacturing and Controls (CMC) knowledge and experience with Common Technical Document content templates as well as content expectations for IND/NDA/BLA/MAA and other regulatory documentation.
- A background of pharmaceutical manufacturing or quality control/quality assurance is a plus.
- A working knowledge of cGMP's is desired.
Knowledge/Skills/Abilities:
- 5 years of experience in medical/technical writing.
- Superior working knowledge of software programs in Windows environment with excellent proficiency in word processing, flow diagrams, and spreadsheets.
- Ability to learn fast, grasp the "essence" of a strategy or a story quickly to convert relevant scientific data/information into high quality summaries and reports.
- Excellent organizational, writing, communication and time management skills needed to manage multiple ongoing projects and/or other writers simultaneously.
