What are the responsibilities and job description for the Quality Engineer position at Tylent?
Position: Manager, Quality Engineering
Location: Columbus, Nebraska (Onsite)
Job Type: Permanent / Direct Hire
Relocation Assistance: Yes
Ideal Candidate:
- Must have high volume quality manufacturing experience. Understand the bridge between quality and production.
- Minimum 5 years’ experience in quality, with a minimum of 3 years in the medical device industry
- Experience with Validations, CAPA, Statistical Analysis.
- Experience with high volume manufacturing processes.
The Manager Quality Engineering is responsible for the management, direction and coordination of all quality and regulatory compliance activities across the designated Columbus Manufacturing BU in compliance with world-wide regulations, business strategies, and customer needs. This includes providing the quality leadership encompassing Quality Systems, Quality Engineering, and Sterilization control to ensure that the required production, quality and regulatory standards are achieved through molding, assembly, packaging, sterilization and product release. Reports to the site Associate Director Quality Management with dotted line reporting to the designated BU Manager.
REQUIREMENTS:
- Bachelor of Science degree in Engineering or Science related field.
- Minimum 5 years’ experience in quality, with a minimum of 3 years in the medical device industry
- Experience with Validations, CAPA, Statistical Analysis.
- Experience with high volume manufacturing processes.
- Experience in Lean/Six Sigma
- Experience managing and leading people required.
- Experience communicating with all levels of the organization
- Capable to manage under pressure and set priorities accordingly.
- Full support to a 24/7 operations.
Salary : $120,000 - $135,000