Description
A leading bio-pharmaceutical organisation requires a Validation Engineer with projects experience and fill finish knowledge. As the validation engineer you will ensure the validation compliance of equipment, systems and processes in both solid dosage forms and sterile products manufacturing.Responsibilities;
- Capable of troubleshooting validation issues associated with projects, process development etc.
- Designs, implements and executes validation studies for manufacturing and control equipment.
- Provide technical assistance on current US FDA and EU validation requirements for Fill Finish manufacture and lyophilization.
- Ensure that the validation status of equipment and systems are in compliance with cGMP at all times.
Key requirements;
- + 7 years experience working in a healthcare manufacturing environment
- projects experience
- sterile experience
- fill finish knowledge
Please apply today with a covering letter highlighting your key skills and relevant experience aligned to this contract opportunity.