Job Description
An exciting opportunity awaits for a manufacturing professional with experience in aseptic or cleanroom environments to handle various tasks. As a key player in new product introductions and clinical manufacturing of small and large molecules, you will be responsible for preparing batches, ensuring area preparation, and collaborating with vendors on system improvements.
* Prepare batches, including vial washing, sterilization, and area preparation.
* Work aseptically as required.
* Perform compounding, filtration, and filling operations.
* Collaborate with vendors on system improvements and process optimization.
* Prepare components and equipment for Grade A environments.
* Operate multi-product suites, ensuring smooth campaign switching.
* Conduct environmental monitoring and testing.
* Fully comply with Good Manufacturing Practices (GMP) and Standard Operating Procedures (SOPs).
Requirements
* Relevant qualification or 18-24 months' experience in the pharma/med device industry.
* Mandatory knowledge of aseptic practices in clean rooms.
* Desirable: Strong knowledge of GMP, quality systems, drug manufacturing, and validation principles.