What are the responsibilities and job description for the Quality Manager position at Cavist Manufacturing?
About us
Cavist is a contract manufacturer specializing in sealing and protecting electronics. We are growing and are honored to have market leading customers in the Automotive, Renewal Energy, Medical Device, Wearable Electronics, Defense, and Aerospace industries.
These customers come to us with groundbreaking and life-changing technologies that typically struggle to survive in the harsh environments of the real world. As worldwide experts in our field, we develop solutions to endure so that they can improve the lives of people worldwide! We get our customers from Vision-to-Volume as quickly as possible, whether it be in thousands or tens of millions of units.
Although Cavist has been in business for over 25 years, we are proud and excited to have just made the transition to an employee owned (ESOP) company.
Are you worthy of joining our awesome team? Do you want to be a cog in a big machine, or do you really want to make a difference? If so, we are eager to meet you and discuss how we can achieve mutual value generation as co-owners in an exciting and dynamic industry.
Profile:
The Quality Assurance Manager is the company’s senior quality professional, reports directly to the President, and is a key member of the leadership team. The ideal candidate will;
- Relish the opportunity for personal growth and to further develop and execute our quality strategy to achieve superior results and key business goals.
- Serve as the primary contact for customers, suppliers, regulatory agencies, and registrars with respect to quality initiatives, including established manufacturing, new product development, and prototyping programs.
- Drive data-based decisions in collaboration with peers, subordinates, customers, suppliers, and other stakeholders in gaining and sharing knowledge to achieve desired outcomes.
- Demonstrate a LEAN mentality, be passionate about timely root cause analysis (RCA) and drive continuous improvement in performance and expectations.
- Champion our continued compliance with ISO Standards (9001, 13485, etc.), internal and external audits, and achieving FDA registration.
- Lead the completion and optimization of our ongoing transition to a digital quality management system.
- Identify, grow, retain, and mentor talent.
Skills & Requirements:
- Bachelor’s degree in engineering or quality related field
- 5 years of experience in regulated manufacturing environment
- Strong understanding of Medical device GMP requirements
- Injection molding and medical device manufacturing experience
- Experience with digital quality management systems
- Auditing Experience
- Lean and six sigma qualifications an advantage
- The candidate must be highly organized and disciplined and be able to demonstrate their ability to meet deadlines
- Strong verbal and written communication skills
- Sitting, standing, walking, bending, reaching overhead, kneeling, balancing, pushing (up to 40 lbs.), pulling (up to 40 lbs.), talking, hearing, repetitive use of hands/arms/legs, grasping, lifting (up to 40 lbs.), carrying (up to 40 lbs.), eye/hand coordination and fine manipulation and extensive computer work
Job Type: Full-time
Benefits:
- 401(k)
- 401(k) matching
- Dental insurance
- Health insurance
- Life insurance
- Paid time off
- Tuition reimbursement
- Vision insurance
Schedule:
- Monday to Friday
Work Location: In person