Quality Assurance Validation Specialist
hace 2 semanas
Mentor Technical Group provides a comprehensive portfolio of technical support and solutions for the FDA-regulated industry.
Our team of experts is dedicated to ensuring compliance with pharmaceutical, biotechnology, and medical device safety and efficacy guidelines.
Key Responsibilities:
- Engineer or Specialist for equipment and process validation including IQ, OQ, TMV/MSA, PQ protocol generation and execution.
- Hands-on with automation, tooling, and maintenance technicians to coordinate and follow-up on equipment troubleshooting, repairs or service required to assure that equipment validation is successful and for resolution of any deviation.
- Good team-member, with communication and time management skills to keep-up with project timeline.
Requirements:
- Engineering preferred, Science or technical background
- 2 years at least in validation engineering/specialist
Mentor Technical Group is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, protected veteran status, disability status, or any other characteristic protected by law.
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