QA / CQV Document Control
Validation & Engineering GroupPuerto Rico, United States
Posted February 8, 2021
Full Time
About the Company
Validation & Engineering Group provides compliance, validation, and engineering services for pharmaceutical, medical device, and biotech companies.
Job Description
The company is a leading services supplier providing solutions for the Pharmaceutical, Biotechnology, Chemical, and Medical Devices industries. The position involves verifying Commissioning, Qualification and Validation Documents, generating data management metrics, and working with Excel and pivot tables.
Requirements
- Bachelor Degree in Science or Engineering
- Not less than 5 years of experience in Pharmaceutical Industry
- QA experience as CQV reviewer preferred
- Excel / pivot tables advanced knowledge is a must
- Highly organized