We are seeking a Sr. Validation Engineer with over 8 years of experience in quality investigations. The ideal candidate will have the following qualifications
Key Responsibilities:
Lead and manage validation activities, focusing on quality investigations.
Perform Commissioning, Qualification, and Validation (CQV) in sterile/aseptic facilities.
Conduct thermal mapping and analyze results to ensure compliance with regulatory standards.
Collaborate with cross-functional teams to address and resolve any issues related to sterilization and SIP (Steam-in-Place).
Qualifications:
Minimum of 8 years of experience in quality investigations within a regulated environment.
Proven experience in CQV for sterile/aseptic facilities is essential.
Extensive experience in thermal mapping is required.