BioTalent are proud to represent a world leading Healthcare and Medical Device pioneer on the search for a Senior Quality Manager - Validation and Risk to join their renowned site in Cleveland Mississippi.
They are seeking an experienced Senior Quality Manager to lead Quality Engineering activities whilst ensuring compliance accordance with FDA guidelines and overall business priorities and schedules.
This role will offer you:
- A genuine opportunity to make a difference, being exposed to a variety of development projects which have the potential to save lives.
- A great opportunity to develop your career within a company that provides continuous career and development opportunities.
- The opportunity to take on more project lines at the site
You will be Responsible for:
- Hardware and software validation
- Integration of Six Sigma methodology into validations, manufacturing and testing processes.
- Implementing paperless systems
- Process monitoring (SPC), data integrity requirements, and risk management oversight activities
- Audits, and creating required changes to specifications and SOPs
- Internal relationships - Liaising with stakeholders and responsible for training growth and development of team
- Managing financial responsibilities and accountabilities - budgeting and expenditures for areas of responsibility.
You will bring the following:
- Bachelor's Degree in Science or Engineering
- Leadership experience
- Circa 7 years within Quality/Manufacturing/Engineering roles
- Six Sigma Black Belt Certification is preferred
