Opportunity Description
Join as a Senior Engineer for Validation Projects, focusing on validation protocols and GMP compliance in the pharmaceutical industry. Embrace a flexible, hybrid work model while leading quality assurance efforts.
With at least 5 years of industry experience, you will oversee and manage all phases of validation activities. Responsibilities include drafting master validation documents, executing protocols, and collaborating with QA teams to meet compliance standards. Your expertise will ensure the success of validation projects while maintaining client relationships.
Key Responsibilities: • Draft comprehensive validation master documents • Execute equipment and process qualification protocols • Ensure compliance with GMP during activities • Aid QA teams in managing change controls • Oversee client account responsibilities
Requirements: • Degree in science, engineering, or relevant field • Minimum of 5 years in validation roles • Strong understanding of GMP reg...
With at least 5 years of industry experience, you will oversee and manage all phases of validation activities. Responsibilities include drafting master validation documents, executing protocols, and collaborating with QA teams to meet compliance standards. Your expertise will ensure the success of validation projects while maintaining client relationships.
Key Responsibilities: • Draft comprehensive validation master documents • Execute equipment and process qualification protocols • Ensure compliance with GMP during activities • Aid QA teams in managing change controls • Oversee client account responsibilities
Requirements: • Degree in science, engineering, or relevant field • Minimum of 5 years in validation roles • Strong understanding of GMP reg...
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