Cleanroom Validation Engineer
Key Responsibilities:
* Commissioning and qualification of new aseptic manufacturing equipment.
* Preparing and executing qualification documentation, including FAT, SAT, IOQ, PQ protocols.
* Providing technical support for the development of user requirements specification (URS) and functional specifications associated with aseptic processing.
* Assisting during investigations or process/equipment issues.
We are currently hiring a Cleanroom Validation Engineer to work on commissioning and qualifying new aseptic manufacturing equipment, preparing qualification documentation, and providing technical support for URS and functional specifications. This role involves ensuring the quality and safety of pharmaceutical products by validating cleanroom environments and manufacturing equipment.
Responsibilities Include:
* Aseptic equipment validation and qualification.
* Development and execution of comprehensive qualification plans.
* Troubleshooting and resolving equipment malfunctions.
* Collaboration with cross-functional teams to ensure seamless integration with production processes.
This is an exciting opportunity for a detail-oriented and analytical professional to join our team as a Cleanroom Validation Engineer. If you have experience in cleanroom validation, equipment qualification, and aseptic processing, we encourage you to apply.
About the Role:
* Perform routine equipment maintenance and troubleshooting.
* Conduct thorough risk assessments and develop mitigation strategies.
* Collaborate with colleagues to optimize processes and improve efficiency.
* Stay up-to-date with industry regulations and best practices.
This position offers a dynamic work environment with opportunities for growth and professional development. If you're passionate about delivering high-quality results and ensuring patient safety, we'd love to hear from you.