About this role
Build More Than a Job—Build a Career at SpiTrex CTE
At SpiTrex CTE, we invest in our people. You’ll find opportunities to grow, real flexibility, and a culture that values balance, development, and teamwork.
Why join CTE?
• Career Growth: Ongoing training and development through Bamboo Path Track & WorkForge
• Flexibility: Flextime options that support real life
• Culture: Team events, Donut Fridays, food trucks, and more
• Rewards: Referral bonuses, quarterly bonuses, and a 401(k) with 50% company match (up to 10%)
• Benefits: No-cost vision, life, and short-term disability; dental & medical with HSA or PPO options
Ready to grow with a company that values you? Join SpiTrex CTE.
1st Shift: Monday to Thursday, 6AM - 3PM; Friday, 6AM - 10AM
Essential Functions:
• Assisting with Customer Audits, Internal Audits, Notified Body Audits, and FDA Inspections
• Assisting with Supplier Management (including but not limited to supplier performance review, and supplier audits)
• Managing Direct Reports
• Developing and implementing quality control procedures and guidelines
• Monitoring and analyzing data to identify areas for improvement
• Initiate quality improvement projects
• Collaborate with cross-functional teams to resolve quality issues
• Conducting audits on products and processes
• Providing guidance to other team members
• Investigating and resolving customer complaints
• Conform to ISO13485, 21 CFR Part 820, and medical device industry requirements
• Reviewing and approving product and process changes
• Developing procedures and work instructions as needed
• Other work-related tasks as assigned
Competency:
• Strong background in quality control and quality engineering functions
• Understanding GD&T
• Experience with Statistical Software
• Experience with Gage Repeatability and Reproducibility
• Excellent communication skills
• Excellent leadership skills
• Detail-oriented
• Strong analytical and problem-solving skills
• Ability to manage multiple projects simultaneously
• Strong understanding of medical device regulations
Educational Requirements:
B.S. in Engineering field preferred or minimum of 5 years in Quality Engineering role
Experience:
5-7 years of Medical Device experience in Quality setting preferred
Benefits Include:
• Medical, Vision and Dental Insurance
• Short-Term Disability
• Life Insurance
• 401(k) - 50% company match (up to 10% contribution)
• Paid vacation days
• Paid holidays