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Main Responsibilities:
1. Manage a team of Quality Engineers/Microbiologists ensuring the site delivers safe and effective products that meet customer needs whilst maintaining compliance.
2. Lead the development and implementation of company-wide quality systems and policy compliance to worldwide regulatory requirements including FDA QSR’s, ISO 13485 & IVDD.
3. Manage and lead the Microbiology, Calibration, and Analytical teams ensuring the highest level of compliance.
4. Manage a team of Quality Technicians/Engineers in the Quality department to achieve individual, team, and site goals.
5. Promote continuous improvement within the department using tools such as Performance Excellence review, Growth Plans, and problem-solving.
6. Support the Site’s auditing process including Generalist for external audits.
7. Make decisions around training and development of staff, changes to quality processes, regulatory compliance, and adequate resourcing preventing negative impact to business strategies.
Education and Experience:
1. Relevant third-level qualification. Engineering/Manufacturing/Science is preferred.
2. Minimum 5 years in Engineering/Manufacturing/Science.
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