Responsibilities:
- The development and maintenance of Quality System procedures.
- Ensuring the site delivers safe and effective products that meet customer needs whilst maintaining compliance.
- Monitoring and maintaining the quality and compliance status of associated quality records.
- Maintaining the quality and compliance status of associated Procedures, work instructions and training materials.
- Presenting and communicating status, report metrics, identify trends potential issues, improvement initiatives, as applicable.
- The review and approval of validation documentation in accordance with divisional policies.
- Basic understanding of design controls and design transfer.
EDUCATION AND EXPERIENCE:
- Relevant third level qualification. Engineering/Manufacturing/Science is preferred.
- Minimum 4 years in the Engineering/Manufacturing/ Scientific field.
- 5-6 years working knowledge of process, equipment, facilities and or software validation either within Quality or Engineering departments
- Experience working in a 21CFR820 and/or ISO13485 regulated industry. May consider experience in pharmaceutical validations.
WHAT WE OFFER
Attractive compensation package that includes competitive pay, as well as benefits such as
- Family health insurance,
- Excellent pension scheme
- Life assurance
- Career Development
- Fantastic new facility
- Growing business plus access to many more benefits.
