Quality Assurance / Commissioning, Qualification and Validation Document Control
Validation & Engineering Group
Quality Assurance / Commissioning, Qualification and Validation Document Control
Validation & Engineering Group
Life sciences validation and compliance consulting
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.
Life sciences validation and compliance consulting
Validation & Engineering Group provides regulatory compliance and engineering consulting for life sciences clients in Puerto Rico and the USA, serving pharma, biotechnology, medical devices, and food sectors. It guides the full product lifecycle, performing commissioning and qualification, computer system, equipment, process, and cleaning validation, drafting quality systems, and ensuring regulatory compliance with FDA and European standards. The firm differentiates itself with hands-on engineering expertise combined with deep regulatory knowledge and broad geographic reach, now enhanced after joining Pinnaql Inc. through an acquisition by 3Boomerang Capital, with founders continuing as partners for continuity. Its goal is to help clients bring products to market faster and more reliably by sustaining GMP-compliant operations and ongoing lifecycle compliance.
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