Validation Specialist
Growing consulting company offering an opportunity to provide value added consulting services to life science company
Responsibilities will include:
Development of validation documentation, including validation plans, user requirements, specifications, test plans, test scripts, traceability matrices, and summary reports
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Execution of validation test deliverables, documentation of test results, and documentation of test incidents/defects
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Participation in client meetings
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Project status reporting and tracking
Required Skill Sets: Professional, self-motivated, focused, and efficient work skills. Must be proficient in the Office suite of applications.
Qualifications: 2-5 years life sciences experience preferred with experience in testing and documentation practices.
Education: Scientific or technical degree preferred
Travel: As required based on client project requirements
Note: Your privacy is important to us so your name, email address, telephone and CV will not be shared outside of QACV Consulting. If you would ever want this information to be deleted from our records, please indicate so by emailing us at contact@qacvconsulting.com.
Call 1+(610) 442-2250
