Description
The activities would include:- Deliver the validation site strategy in a safe, compliant manner and to the highest standard of performance.
- Planning, execution and reporting the on-going validation compliance of facilities, equipment, systems and processes in both solid dosage forms and sterile products manufacturing.
- Maintain compliant validation systems/processes on-site, including the maintenance of the site validation master plans.
- Provide validation expertise, technical support and knowledge to site cross functional teams.
- Assessment, review and approval of change controls to maintain validation status.
- Actively participate in a positive team environment where support, challenge, empowerment and continuous learning/knowledge exchange is encouraged.
- Preparation and maintenance of departmental metrics to internal and external stakeholders
Qualifications
- Degree in Science, Engineering or related area
- 3-4 years experience working in a Pharma/Biopharma/Healthcare manufacturing environment. Skills & Knowledge
- Competent technical knowledge of facility / utility / equipment / process / cleaning / computer systems validation for solid oral dosage and sterile manufacturing facilities.
- Clean Steam experience needed
- Strong background in pharmaceutical utilities qualification / qualifying including water, steam, purified water.
- Detailed knowledge of quality management systems.
- Good communication skills at organisation, team and individual levels.
- Ability to use MS Project and SPC packages an advantage
If you would like to apply please contact me on or alternatively reply with a copy of you most recent CV. We also offer shopping vouchers for any successful referrals so if you know of anyone who is looking please feel free to get in touch.