Description
Role:- To coordinate the Process and Cleaning Validation programmes.
- To aid and participate in technical investigations in support of the various groups on site in particular the Manufacturing department.
- Generate and execute documentation in relation to the Process and Cleaning Validation programmes including Master Validation Plans, Protocols, and Reports in line with cGMP, EU, FDA and Risk MaPP guidelines.
- Carry out investigations, where necessary, associated with validation batches.
- Communicate and liaise with other departments/stakeholders who impact on, or are impacted by, the validation programme.
- Participate in the quality management systems including investigations, deviations and change control.
- To provide technical support as required
Qualifications and essential functions for this position:
- 3rd level qualification in a science related discipline.
- A minimum of three years experience in a similar role.
- Specific experience in Cleaning Validation (Solid Dosage preferable) is required.
- Good knowledge of manufacturing processes is required.
- Knowledge of process validation would be a distinct advantage.
- Good verbal and written communication skills
- Excellent trouble shooting and problem solving skills
- Good computer skills (MS Word, Excel and PowerPoint)
- Good attention to detail
- Ability to think logically and be proactive.
- Ability to work as part of a team and on own initiative in a constructive manner
- Flexible and self motivated
An excellent salary is on offer alongside benefits package including: pension, healthcare and bonus.
Apply now for immediate consideration