Job Description
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 teamKey ResponsibilitiesValidation 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 havesGxP 4/5Computer System Validation (CSV) 4/5Jira 3/5
Skills Required
Gxp, Rim, Jira
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 teamKey ResponsibilitiesValidation 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 havesGxP 4/5Computer System Validation (CSV) 4/5Jira 3/5
Skills Required
Gxp, Rim, Jira
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