Job Description :
This is a nine month assignment in South San Francisco, CA, with potential for extension based on performance.
9 Months

Need local only

Overview:
Work with an up and coming company who is focused on developing and commercializing novel therapies in the field of Oncology.
The company is currently in the process of completing multiple clinical trials, and they need additional support due to an ramp up in clinical trials.
The primary responsibility of the Technical Writer will be to write and/or revise the written content of Standard Operating Procedures (SOP’s) to be used by the client''s Manufacturing and Global Supply Chain department.

Primary Responsibilities:
Create new or revise existing content for SOPs with a high degree of quality in accordance with cGMP requirements and corporate guidelines
Work collaboratively with project team members including Manufacturing, Analytical Development, Global Supply Chain, Quality and other subject-matter experts to solidify content.
Ensure SOPs are completed on schedule.

Technical Must Haves:
BS Degree in Science/Life science
3+ years related experience in technical writing
Experience in a Quality environment, and knowledge of GMP and/or ISO standards.
Experience writing SOPs from scratch in pharmaceutical and/or biotech manufacturing environment an asset.
Ability to work well with others and translate verbally received technical information and details into written SOPs.