QA / CQV Document Control
- Full-time
Company Description
Validation & Engineering Group, Inc. is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, among other services.
Job Description
Document Control / Data Management
Will verify Commissioning, Qualification and Validation Documents as needed.
Will Generate data management metrics.
Will work with Excel and pivot tables.
Administrative and Non Standard Shift.
Qualifications
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.
Additional Information
More Positions available for Puerto Rico and USA.
Validation and Engineering Group, Inc is an Equal Employment Opportunity employer.