QA / CQV Document Control

Validation & Engineering Group; Juncos (PR); On-site; USD 70,000 - 90,000; Full time

Job summary

A leading engineering firm in Puerto Rico seeks a skilled professional for document control and data management tasks. Responsibilities include verification of commissioning, qualification, and validation documents, as well as generating metrics using advanced Excel skills. Candidates must have a Bachelor's Degree in Science or Engineering and at least 5 years of experience in the Pharmaceutical Industry. QA experience as a CQV reviewer is preferred. This position offers varied working shifts.

Qualifications

• 5+ years of experience in the Pharmaceutical Industry is required.
• QA experience as a CQV reviewer preferred.
• Advanced knowledge of Excel and pivot tables is necessary.

Responsibilities

• Document Control and Data Management responsibilities.
• Verification of Commissioning, Qualification and Validation Documents.
• Generation of data management metrics.

Skills

Document Control

Data Management

Excel

Organizational Skills

Education

Bachelor's Degree in Science or Engineering

Job description

Responsibilities

• 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 advancedknowledge is a must.
• Highly organized.

Additional Information

• More Positions availablefor Puerto Rico and USA.

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