

New · posted Nov 11
Integer · Medical Devices
Quality Engineer II
- Plymouth, MN
- On-site
- Full-time
- Senior & Principal
The role
The primary purpose of this job is to provide Quality Engineering support for Operations to ensure that the Quality System requirements are adhered to for medical device manufacturing/operations in accordance with applicable Regulatory and Standards requirements for compliance. Provide work direction for 1-3 Technicians/Inspectors.
By living according to a common set of values, we create a culture that unifies, embraces the uniqueness we all bring to the company, and positions Integer for long-term success.
At Integer, our values are embedded in everything we do.
Customer
We focus on our customers’ success
Innovation
We create better solutions
Collaboration
We create success together
Inclusion
We always interact with others respectfully
Candor
We are open and honest with one another
Integrity
We do the right things and do things right
What you need
· Minimum Education: Bachelor’s Degree in Engineering or related field required.
· Minimum Experience: 2-5 years quality engineering experience, preferably in medical device or regulated manufacturing
Accountabilities & Responsibilities
·Adheres to Integer Core Beliefs and all safety and quality requirements including, but not limited to: Quality Management Systems (QMS), Environmental Management Systems (EMS), U.S. Food and Drug Administration (FDA) regulations, Company policies and operating procedures, and other regulatory requirements.
·Support regulatory and agency inspections, audits, investigations, and inquiries regarding the control and assessment of product design and manufacturing quality.
·Monitor manufacturing of assigned products, assuring compliance with DMR while providing deviation/waiver guidance and assuring complete and correct Device History Records are maintained.
·Review the adequacy and correctness of changes to Bill of Materials (BOM’s), Assembly Procedures, Drawings, Component Specification, FMEAs, Control Plans, etc.
·Lead generation and completion of protocols and reports for test method validations.
·Interfaces with Manufacturing Engineers to review processes for new and existing products and coordinate process validations and capability studies. Recommends process monitoring devices where applicable.
·Develops various inspection techniques and procedures to ensure product integrity to design specifications. Responsible for the writing, approval and implementation of Incoming, In-Process and Final Inspection procedures.
·Ensure that the disposition of non-conforming materials meet all necessary regulatory requirements and assure adequacy of corrective actions to prevent re-occurrence.
·Lead and manage complaint investigations.
·Participate in plant CAPA activities, including analysis of data and trends in complaints, supplier quality, nonconforming material, training effectiveness, and root causes analysis.
·Participate in continuous improvement projects.
·Assist with product transfers.
·Works with suppliers, management, Engineers and Manufacturing associates in the resolution of quality problems. Also, assists each of these groups with capability studies and the application of statistical quality control which include Cpk, DOE, Hypotheses Testing, etc.
·Mentor and support quality inspectors and technicians.
·Performs other functions as required
Knowledge & Skills
· Special Skills: Ability to work independently and in team environment. Ability to effectively communicate written and verbally. Ability to manage time effectively to ensure timely completion of tasks.
Specialized Knowledge
Competence in the selection and use of Quality Engineering Tools and Techniques.
Good knowledge in the interpretation and application of relevant Domestic and International Regulations and Industry Standards (e.g. ISO, QSR, UL, MDD, TGA etc.)
Proficient in Microsoft Office and Minitab
Our total rewards program is designed to attract, retain, and motivate associates to contribute to Integer’s success. Our compensation program includes base salary and a cash-based incentive program supporting our pay-for-performance philosophy. We provide a comprehensive benefits package with immediate eligibility including medical, dental, vision, disability, life insurance, and adoption benefits. Parental leave is available after one year. Optional employee-paid programs include supplemental life insurance, critical illness, hospital indemnity and accident insurance. Employees are immediately eligible to participate in the 401(k) plan with company matching contributions. We provide 80 hours (10 days) of company designated holidays per year plus an annual allotment of paid time off.
Pay and benefits
$78,375 – $114,950 a year
Employer providedQuality Engineer II Salary: $78,375.00- $114,950
Medical, dental and vision insurance
Disability and life insurance
401(k) with company match
Paid time off and 10 paid holidays
Parental leave after one year
Cash-based incentive program
Where you'll work
Plymouth, MNOn-siteOpen in Maps (opens in a new tab)
More jobs in Plymouth, MNEqual opportunity, accessibility and legal noticesInteger's statements, word for word
U.S. Applicants: Equal Opportunity Employer. In addition, veterans and individuals with disabilities are encouraged to apply.
Job intelligence
The context around this role
Live data · November 11, 2026
Salary intelligence
How the pay compares
This role's midpoint is 22% below the US median for Quality Engineering roles at this level.
This roleEmployer provided
Senior & Principal roles in Minnesota14 roles publishing pay
Senior & Principal roles in the US103 roles publishing pay
| Annual base pay | Low | Median | High |
|---|---|---|---|
| This role | $78,375 | — | $114,950 |
| Minnesota (middle half) | $94,000 | $99,250 | $111,750 |
| All US (middle half) | $104,500 | $123,500 | $138,500 |
This role: Integer's own published range. Comparisons: the base pay employers published on open Quality Engineering roles at the same level on Regulatory Jobs, November 11, 2026. Nothing is estimated.
Career trajectory
Where this role sits in Quality Engineering
The general path across 218 open Quality Engineering roles on Regulatory Jobs, with the titles they carry most. Not Integer's own promotion track.
Skills DNA
What this role leans on
How many of the posting's 31 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- GMP and compliance6
- Documentation and SOPs5
- Investigations and CAPA5
- Quality systems and risk5
- Collaboration and leadership5
- Lab testing and methods2
- Validation and qualification2
- Regulatory submissions1
- Data and digital systems1
- Clinical trial conduct1
Regulatory intelligence
The rules, regulations and standards behind this role
The regulations, guidance and standards that govern Quality Engineering work in medical devices, led by the one this posting names, each linked to the agency or standards body that publishes it.
- TGAAustralia TGA(official source, opens in a new tab)Australia's Therapeutic Goods AdministrationNamed in the posting
- FDA21 CFR Part 820 (QMSR)(official source, opens in a new tab)FDA quality management system regulation for medical devices, aligned with ISO 13485
- ISOISO 13485(official source, opens in a new tab)Quality management systems for medical devices
- ISOISO 14971(official source, opens in a new tab)Application of risk management to medical devices
- ISOISO 2859-1(official source, opens in a new tab)Sampling procedures for inspection by attributes (AQL sampling plans)
- FDA21 CFR Part 803(official source, opens in a new tab)Medical device reporting of deaths, serious injuries and malfunctions
- ISOISO 19011(official source, opens in a new tab)Guidelines for auditing management systems
- IECIEC 62366-1(official source, opens in a new tab)Application of usability engineering to medical devices
- ISOISO 10993-1(official source, opens in a new tab)Biological evaluation of medical devices within a risk management process
- ISOISO 11135(official source, opens in a new tab)Ethylene oxide sterilization of health care products
- ISOISO 11137-1(official source, opens in a new tab)Radiation sterilization of health care products
- ISOISO 11607-1(official source, opens in a new tab)Packaging for terminally sterilized medical devices
- ISOISO 11737-1(official source, opens in a new tab)Determination of the microbial population (bioburden) on medical devices
- FDAFDA Computer Software Assurance(official source, opens in a new tab)Risk-based assurance for production and quality system software
- FDA21 CFR Part 806(official source, opens in a new tab)Reports of medical device corrections and removals
- EUEU MDR (Regulation 2017/745)(official source, opens in a new tab)The EU Medical Device Regulation: CE marking, technical documentation, vigilance
Company hiring pulse
Integer on Regulatory Jobs
- 19
- Open roles
- 19
- Distinct roles
- 11
- Locations
By discipline
- Quality17 89%
- Regulatory2 11%
By level
- Associate & Specialist10 53%
- Senior & Principal6 32%
- Manager3 16%
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Quality Engineer II at Integer
Open until filled. $78K–$115K a year, employer provided.


