The Opportunity

We're looking for a Technical Writer II, working in the IT (excluding Telecommunication) industry in Mountain View, California, United States.

  • Writes and edits high-level quality for a quality management system.
  • Works as a document control specialist in which you will be responsible for change control of all documentation within the quality management system.

We are offering Competitive Compensation and Benefits. This position may present an opportunity to go permanent.

Our Client

Our client is an award-winning clinical development company.  Improving lives globally with 20+ years experience in clinical research and strategic resourcing.  Elevating results with proven strategies, comprehensive solutions, and customized delivery models.

Serving pharmaceutical, biopharmaceutical, biotechnology, and medical device organizations.

Strong relationships provide you connections and access to great opportunities.  Industry expertise sets you up for success with helpful insights, career coaching, and professional training.  Grow and learn while you put your skills to work.  

Experience Required for Your Success
  • Bachelor degree or higher in Technical Communication, English, or a related field
  • 2-5 years of experience as a technical writer
  • 3+ years writing for the medical device industry
  • 2+ years operating with ISO13485:2016 & 21 CFR Part 820
  • Proficient in GSuite/Microsoft Office Project management skills.
What Do You Think?

Does your experience reflect what it takes to be successful in this role? Do the work and challenges get you excited about what's possible? Apply here.

Not exactly? Join Our Talent Community, and we'll let you know of additional opportunities.


Optional. 20 MB file size limit. Supported file types.

Upload your Resume
I have read and accepted the Terms & Privacy Policy
I agree to be part of PSG's Talent Community and be profiled to other jobs that match my skills