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.
