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Medical Devices Quality Supervisor Jobs (NOW HIRING)

Abbott

Senior Supervisor, Quality Control

Sylmar, CA · On-site

The Sr. Quality Supervisor is responsible for the performance of his or her team and meeting any ... Knowledge of applicable regulations and standards affecting the manufacture of Medical Devices (i.e ...

Hologic, Inc.

WI · On-site

$138K - $230K/yr

Supervisory Responsibilities * None Qualifications Education Basic Qualifications * B.S. in ... ISO 13485:2016 - Medical devices - Quality management systems - Requirements for regulatory ...

Langham Logistics

Quality Supervisor

Easton, PA · On-site

Minimum 3 years of hands-on Quality experience in a strict, cGMP-regulated environment (Pharma, Biotech, or Medical Devices). * Leadership: Previous supervisory or managerial experience is required.

Integrated Resources INC

Quality Engineer I

Pleasanton, CA · On-site

$80K - $103K/yr

Job title: Quality Engineer I Location: Pleasanton, CA Duration: 7+ months (Possibility of ... Utilizes detailed understanding of the clinical environment and the use of medical devices, to ...

Verstela

Quality Supervisor

Mesa, AZ

$82K - $103K/yr

This Direct Hire Quality Supervisor opportunity offers the chance to lead a skilled team, drive ... Medical * Dental * Vision * 401(k) Retirement Plan with Company Match * Profit Sharing * Paid ...

V2X

The Quality Supervisor (Medical) monitors, evaluates, and ensures the quality, compliance, and ... devices. * Must comply with all Fire and Safety Regulations and post policies. At V2X, we are ...

Collate

Quality Engineer: Medical Devices

San Francisco, CA · On-site

$84K - $109K/yr

We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential ...

A-Line Staffing Solutions

Be Seen First

Assembler - Medical Devices

Sandy, UT · On-site

$25/hr

Assembler - Medical Devices Location: Sandy, UT Schedule: M-F 8am - 5pm Pay Rate: $25/hour LOOKING ... quality concerns to engineering and supervisory personnel * Support continuous improvement ...

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Medical Devices Quality Supervisor information

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$38.5K

$91K

$138.5K

How much do medical devices quality supervisor jobs pay per year?

As of Sep 13, 2026, the average yearly pay for medical devices quality supervisor in the United States is $91,047.00, according to ZipRecruiter salary data. Most workers in this role earn between $70,500.00 and $110,000.00 per year, depending on experience, location, and employer.

What are popular job titles related to Medical Devices Quality Supervisor jobs?

For Medical Devices Quality Supervisor jobs, the most frequently searched job titles are:

Quality Manager - Medical Devices

Harleysville, PA • On-site

Martech Medical Products
Manufacturing • 201 - 500 employees
Learn more about Martech Medical Productsexternal

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 13 days ago

Job description


Quality Manager
Full-Time | Onsite
*This position is not eligible for relocation assistance or employer-sponsored work authorization.  Candidates must be legally authorized to work in the United States and not require sponsorship now or in the future.
Lead Quality. Drive Excellence. Impact Patient Care.
At Martech Medical Products, quality is more than compliance. It's a commitment to the patients who depend on the medical devices our customers bring to market.
We're looking for an experienced Quality Manager to lead our Quality Engineering and Quality Control teams and help shape the future of our quality organization. This is a high-impact leadership role where you'll influence manufacturing excellence, regulatory compliance, operational performance, and continuous improvement across the facility.
If you're passionate about building strong teams, driving process improvements, and creating a culture where quality is everyone's responsibility, we'd love to hear from you.
What You'll Do
As Quality Manager, you'll serve as a key member of the site leadership team and be responsible for the overall effectiveness of our Quality Management System while ensuring compliance with FDA and international quality standards.
Key Responsibilities
  • Lead Quality Engineering and Quality Control teams to achieve quality, compliance, and operational objectives.
  • Maintain and continuously improve the Quality Management System (QMS) in accordance with FDA QMSR (21 CFR Part 820), ISO 13485, ISO 14971, and applicable regulatory requirements.
  • Drive quality system initiatives, including CAPA, internal audits, nonconformance management, complaint investigations, and change control activities.
  • Lead risk management efforts and promote risk-based decision making across manufacturing and business processes.
  • Partner with Manufacturing and Engineering to support process validations, equipment qualifications, automation initiatives, and new product introductions.
  • Monitor quality metrics and implement continuous improvement initiatives that improve performance, reduce risk, and enhance customer satisfaction.
  • Support cleanroom manufacturing operations, contamination control programs, and ongoing audit readiness.
  • Lead root cause investigations and implement effective corrective and preventive actions.
  • Serve as the primary quality representative during customer, certification body, and regulatory audits.
  • Develop, coach, and mentor a high-performing quality team while fostering a culture of accountability, collaboration, and continuous improvement.
  • Collaborate with Operations, Engineering, Supply Chain, and Regulatory Affairs to ensure product quality, regulatory compliance, and operational effectiveness.

What Success Looks Like
In this role, you'll:
  • Build and develop a strong, engaged quality team.
  • Ensure sustained compliance and audit readiness.
  • Strengthen quality systems and risk management processes.
  • Improve operational performance through data-driven decision making.
  • Partner cross-functionally to solve complex manufacturing and quality challenges.
  • Create a culture where quality is embedded in every process and decision.

What We're Looking For
Required Qualifications
  • Bachelor's degree in Engineering, Quality, Manufacturing, Life Sciences, or a related technical discipline.
  • 8+ years of progressive experience in Quality Assurance, Quality Engineering, or Quality Systems within the medical device industry or another highly regulated manufacturing environment.
  • 3+ years of leadership experience managing quality or technical teams.
  • Strong knowledge of FDA Quality System Regulations (QMSR/21 CFR Part 820), ISO 13485, and quality system requirements.
  • Experience leading CAPA, audits, nonconformance programs, risk management activities, and continuous improvement initiatives.
  • Strong analytical, problem-solving, communication, and leadership skills.
Preferred Qualifications
  • ASQ Certified Quality Engineer (CQE), Certified Quality Auditor (CQA), or similar certification.
  • Lean Six Sigma Green Belt or Black Belt certification.
  • Experience with ISO 14971 risk management methodologies.
  • Experience supporting Class I, II, and/or III medical devices.
  • Experience with process validation, SPC, MSA, and statistical analysis tools such as Minitab or JMP.
  • Experience with supplier quality management and audit programs.

Why Join Martech Medical Products?
This is an opportunity to take ownership of a critical leadership function within a growing medical device manufacturing organization.
You'll have the chance to:
✅ Lead and develop a talented quality team
✅ Drive strategic quality initiatives and continuous improvement efforts
✅ Influence business decisions at the leadership level
✅ Partner with cross-functional teams to solve meaningful challenges
✅ Help ensure the manufacture of products that support patient care worldwide
Benefits & Perks
Martech Medical Products offers a competitive compensation and benefits package designed to support the health, financial well-being, and work-life balance of our employees, including:
  • Medical Insurance
  • Dental Insurance
  • Prescription Drug Coverage
  • Vision Insurance
  • Flexible Spending Accounts (FSA)
  • Company-Paid Life Insurance
  • 401(k) Retirement Plan with Generous Company Match
  • Paid Holidays
  • Paid Time Off (PTO)
  • Professional Development and Career Growth Opportunities
If you're a collaborative leader who thrives in a fast-paced, regulated environment and is passionate about quality excellence, we encourage you to apply.
Martech Medical Products is an Equal Opportunity Employer and is committed to creating an inclusive workplace for all employees. We consider all qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, protected veteran status, or any other characteristic protected by applicable law.
 

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