Validation Project Manager (Consultant)
- Manage project plans and delivery for risk management in a large-scale Biopharmaceutical facility.
- Develop communication plans for risk management related to operations readiness.
- Conduct weekly meetings and deep dive sessions to monitor milestone objectives.
- Lead response and action plans for issues affecting on-time, high-quality operations readiness.
- Bachelor's degree in engineering, Computer Science, or a related field.
- Minimum of 5 years of experience in CSV and validation within the pharmaceutical or biopharmaceutical industry.
- Strong expertise in validating project management in biopharmaceutical environments.
- In-depth knowledge of regulatory requirements (FDA, EMA, etc.) and industry standards (GAMP, 21 CFR Part 11) related to CSV and validation.
- Excellent problem-solving skills and the ability to analyze complex systems and processes.
- Ability to collaborate effectively with cross-functional teams.
- Proactive mindset with a strong attention to detail and the ability to prioritize tasks effectively.
- Experience working in a regulated GxP environment.
- Premium medical coverage
- 401(k) with company match
- Tuition reimbursement
- Unique performance incentives
- And more — all designed to support your growth, well-being, and future.
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