Are you a CMC, process development or validation specialist? Maybe a bit of all three?
This is a unique and fantastic opportunity to join one of Europe’s leading healthcare and pharmaceutical businesses as they continue their expansion across the UK and Europe.
Working in a small facility in Greater Manchester, this position will be responsible for helping to establish new processes for product introduction and commercial scale up. In addition to this, there will be responsibility for full life cycle validation activities across a range of laboratory and manufacturing equipment.
Given the site size and business culture, this role requires a hands on, “can do” approach. Strong stakeholder skills are as crucial as your technical capability.
For further details, please apply or contact Mark Bux-Ryan.
Key experience:
- Experience or knowledge of the radiopharmaceutical industry
- Experience in process development or technical transfer from R&D through to manufacturing
- Validation knowledge and experience
- GMP experience beneficial, although if you have worked within the right technical product categories and have a strong depth of experience across the rest of the role profile, this may not be required
- Strong stakeholder management skills
