Overview
Remote
On Site
$DOE
Accepts corp to corp applications
Contract - W2
Contract - to 01/13/2026
Skills
Pharmaceutics
Veeva
LIMS
Quality Control
Documentation
Change Control
Technical Writing
Writing
Analytical Skill
Crystal Management Console
Collaboration
Quality Assurance
Filing
Job Details
Job Title : CMC Technical Writer ( in QA, Viva/LIMS, pharmaceutical )
Job Location: Santa Monica, California Remote role
Job Duration: 6 months; May extend
Job Location: Santa Monica, California Remote role
Job Duration: 6 months; May extend
7-10 years of experience in the pharmaceutical/biotech industry with expertise in QA systems, regulatory filings, and change controls.
Proficient in Veeva/LIMS and quality control documentation including deviations and change control processes.
Strong technical writing skills, particularly in writing about analytical methods related to quality activities.
Background in analytical development and support for CMC regulatory filings.
Ability to lead and collaborate within a team of 3-5 people.
Cardiology experience is a plus, but not required.
2-round interview focusing on QA expertise and regulatory filing experience.
Proficient in Veeva/LIMS and quality control documentation including deviations and change control processes.
Strong technical writing skills, particularly in writing about analytical methods related to quality activities.
Background in analytical development and support for CMC regulatory filings.
Ability to lead and collaborate within a team of 3-5 people.
Cardiology experience is a plus, but not required.
2-round interview focusing on QA expertise and regulatory filing experience.
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