Integra LifeSciences in Massachusetts seeks a Senior Validation Specialist to lead qualification and validation activities for NPI, transfers, and related projects. You will develop and review protocols, support risk analysis, and ensure compliance with cGMP, QSR, ISO and related standards.
The ideal candidate has a strong engineering or science background, 8+ years in validation/QA for medical devices or pharma, and proven project management and technical writing skills.
#J-18808-LjbffrSenior Validation Engineer II – Med Device Quality in braintree at Unknown Company
This position is listed as full time and onsite.