QA / CQV Document Control

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.

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.

More Positions available for Puerto Rico and USA.

Validation and Engineering Group, Inc is an Equal Employment Opportunity employer.