
Tech Transfer Specialist
- Dublin
- Contract
- Full-time
- Our client has developed a stand-out culture of innovation, inclusion and development, and consistently features as a great place to work.
- This is an excellent opportunity to join a world class manufacturing operation, with an outstanding track record of reliably delivering high-quality medicines to patients around the world suffering serious illnesses.
- Excellent contracting rates on offer.
- Developing and implementing TT Strategy including Process Validation, Control Strategy.
- This includes drug substance and drug product (biologic) and small molecule drug substance and drug product (e.g. oral solid dosage)
- Leading technical gap assessment & ensuring implementation of any associated mitigation activities.
Provide SME input to technical aspects of IR response. * Providing support to Regulatory audits as needed.Support the implementation of TT and Validation best practices across the network, work closely with other members of the ATO TT and Validation team on implementation of improvements.What you need to apply:
- 6 years’ experience providing technology transfer project support to drug substance or drug product manufacturing.
- Proven ability to successfully manage Tech transfer programs at site level and corporate level in support of GMP operations.
- Comprehensive understanding of Technical/cGMP requirements for Tech Transfer activities.
- Ability to present and defend tech transfer topics during regulatory agency inspections.
- Experience of biopharmaceutical Bulk Drug Substance (BDS) manufacturing and aseptic fill finish.
- Extensive knowledge of regulations, current industry practices, and experience of interpretation and application of guidelines and regulations.