I'm delighted to be recruiting for a number of Manufacturing Technician roles with one of our top pharmaceutical clients, based in Mayo. This is a shift role, and 24/7 shift is the eventual goal, so applicants must be open to eventually working night shift and weekend. Shift allowance will be 33%. Salary is dependant on experience. My client is open to someone with Cleanroom experience, and also open to candidates from mechanical or electrical backgrounds with GMP experience.
As our new Manufacturing Technician, you will be responsible for all manufacturing activities necessary to support a tech transfer of a NPI to accommodate clinical manufacture of small and large molecule products. Your new duties will involve (1) Manufacturing, (2) Biologic Drug Product commercial support, and (3) New Product Introduction/Project Management.
As part of a team, you will be responsible for ensuring that drug product manufacturing is performed in compliance with site and GMP procedures, and that scheduling and manufacturing meets global request timelines. Flexibility around shifts will be required.
If great benefits, a defined career path, and work-life balance are important in your next career move, then read on to find out more:
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.
