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

  • Execution of validation test deliverables, documentation of test results, and documentation of test incidents/defects

  • Participation in client meetings

  • 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

 

 

To apply for one of these positions please complete the information below and upload a current copy of your CV.

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

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