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Senior Quality Engineer

CTE Solutions
Posted 11 days ago, valid for 23 days
Location

Plymouth, IN, US

Salary

Competitive

Contract type

Full Time

Life Insurance

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Sonic Summary

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  • SpiTrex CTE is seeking a Quality Engineer with 5-7 years of experience in the medical device industry.
  • The position offers a salary that is competitive and includes a 401(k) plan with a 50% company match up to 10%.
  • Key responsibilities include assisting with audits, managing direct reports, and developing quality control procedures.
  • Candidates should have a strong background in quality control, excellent communication skills, and the ability to manage multiple projects.
  • The company promotes a culture of growth, flexibility, and teamwork, with benefits including medical, vision, and dental insurance.

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



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