Advance as a Senior Engineer in Pharmaceutical Validation, focusing on validation processes, quality assurance, and GMP compliance in a flexible working environment that promotes professional growth.The ideal candidate will possess a minimum of 5 years of relevant experience in validation and qualification of pharmaceutical equipment. You will be responsible for drafting important documentation, executing protocols, and supporting clients’ QA and compliance teams through effective management of validation activities and client accounts.Key Responsibilities:• Create main validation documents like the Validation Master Plan• Execute equipment/system qualification protocols• Ensure GMP compliance for validation activities• Assist clients in managing deviations and CAPA actions• Handle client account management efficientlyRequirements:• Relevant bachelor’s or master’s degree required• 5 years experience in the pharmaceutical industry required• Solid understanding of GMP standards• Familiarity with manufacturing processes is necessary• Willing to travel frequently for client engagementsMake your mark by enhancing quality and compliance across pharmaceutical validations in a supportive and innovative firm.#J-18808-Ljbffr
Senior Engineer In Pharmaceutical Validation
LAPORTE
toronto, toronto
Published 27 days ago
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