Job Summary
We are seeking a skilled Sterilization Validation Engineer to join our team. In this role, you will be responsible for ensuring the sterilization of medical devices is compliant with regulatory standards.
About the Role
* Support routine sterility assurance activities such as GMP compliance, cleanroom risk assessments and supplier change control
* Develop and implement inspection methods for products and production equipment
* Maintain compliant documentation
What We're Looking For
Pursuing a degree in Engineering or Science, preferably related discipline.
1–2 years' experience in regulated manufacturing or medical device environment,
knowledge of GMP regulations
, strong analytical skills,
and ability to work collaboratively within cross-functional teams. -----------------------------------