Job Description & How to Apply Below
4 to 6 years of experience in GxP, Computer System Validation (CSV), and Life Sciences.
Proficiency in Veeva QMS, RIM, and eTMF systems is add on.
Strong knowledge of regulatory compliance within the Life Sciences industry, including FDA regulations.
Excellent problem-solving and communication skills.
Ability to work both independently and as part of a team
Key Responsibilities Validation Testing - Conduct validation and verification testing to ensure that software products meet specified requirements and perform as expected.
Documentation - Prepare, review, and maintain validation documentation, including test plans, protocols, reports, and other relevant documents.
3 must haves
GxP 4/5
Computer System Validation (CSV) 4/5
Jira 3/5
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