About the job
Job Overview
Verista, a leader in providing innovative solutions for the life sciences industry, collaborates with renowned brands to address critical business challenges. Our mission is to foster growth and innovation within the scientific community and assist researchers and organizations in overcoming significant healthcare obstacles. We pride ourselves on delivering services that empower informed decision-making, backed by our substantial investment in our workforce and capabilities.
Our success is fueled by a team of world-class professionals who excel in collaborative environments, sharing our vision to enhance the lives of clients in the life sciences sector. Our dedicated experts are resolute in their commitment to making a daily impact.
Company Culture and Values:
- We empower and support our colleagues.
- We are dedicated to client success at every opportunity.
- We demonstrate the courage to do what is right.
- We cultivate an inclusive environment where all colleagues feel respected, engaged, and challenged.
- We continuously seek to expand our skills and learn from our experiences to elevate our collective expertise.
Key Responsibilities of Validation/CQV Engineer:
- Develop, revise, and execute technical documentation related to commissioning, qualification, and validation for standard equipment, systems, software, and processes under the guidance of the project leader.
- Execute test scripts and accurately document results.
- Ensure compliance with project timelines for all assigned tasks.
- Maintain comprehensive and detailed records pertaining to qualification and validation processes.
- Interpret technical schematics to identify and test photo sensors, confirm part numbers, and perform input/output testing on automated manufacturing equipment.
