Description:
Key activities you will perform in the role:
- Manufacturing of pharmaceutical products at different stages of lifecycle including clinical, non-clinical and pre-clinical material.
- Batch preparation activities (vial washing, load sterilization, area preparation).
- Work aseptically or as required by the classification of the production area(s)
- Perform compounding, sterile filtration and sterile filling activities
- Work with various vendors on the development/improvement of new and existing systems regarding single use technologies.
- Prepare components and equipment for processing into Grade A environments
- Aid in running a multi-product suite, changing between different product campaigns without issue.
- Perform environmental monitoring
- Comply with Good Manufacturing Practices (GMP) and with Standard Operating Procedures (SOPs)
- Review and contribute to technical documents, including protocols, reports and batch manufacturing documents
- Participate in cross-functional teams with other functions, including R&D, Engineering, Quality, Supply Chain, Operations and Validation
- Adhere and support all EHS standard procedures and policies.