Senior Validation Specialist
3 weeks ago
Valspec, a leading provider of system validation and lifecycle services, is seeking an experienced Validation Engineer to join their team. The ideal candidate will have a proven track record in the SDLC of automated computer systems within biopharmaceutical environments.
Key Responsibilities:
- Develop and execute validation protocols for automated process equipment.
- Generate validation protocols, summary reports, and protocol exceptions.
- Schedule and execute qualification activities.
- Update documentation, including IQ, OQ, PQ, and other related validation documentation.
- Represent the validation and qualification teams in meetings and project coordination.
Requirements:
- 5+ years of equipment validation experience in an aseptic fill or similar environment for pharmaceutical manufacturing.
- Equipment and/or Computer System Validation (CSV) experience within a life sciences manufacturing environment.
- Direct experience developing validation protocols and executing protocols.
- Experience generating validation protocols, summary reports, and protocol exceptions.
- Scheduling and execution of qualification activities.
- Documentation updates, including IQ, OQ, PQ, and other related validation documentation.
- General meeting attendance and project coordination representing validation and qualification teams.
What We Offer:
- A competitive salary range of $110,000 per year.
- A standout culture and fantastic work environment.
- Competitive benefits, including premium medical, 401K match, profit sharing, tuition reimbursement, and other unique incentives.
Valspec is an Equal Opportunity Employer and is committed to providing a professional environment free of any discrimination or harassment. We are proud to be a Drug-Free Workplace.
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