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Salary
$78k – $115k per year
Location
In office (Plymouth)
Seniority
Middle · 2+ years exp
Visa
H-1B filings in 12 months: 1
Employment
Full-Time

Confirmed on the employer's own hiring board on Nov 10, 2026. First seen by Alion on Nov 10, 2026. Integer scores B on the Alion truth index.

Overview
Company
Impact
Profile match
Integer is a medical device contract development and manufacturing company headquartered in Plano, Texas, making components, subassemblies and finished devices for cardiac rhythm management, cardiovascular, neuromodulation and other medical device makers. Formerly Greatbatch, it took the Integer name in 2016 after acquiring Lake Region Medical, is listed on the New York Stock Exchange, and runs plants in the US, Mexico, Ireland, Uruguay and the Dominican Republic, plus Electrochem specialty batteries. It hires manufacturing team members and operators, machinists, quality inspectors, manufacturing and materials engineers, supply chain and purchasing staff and IT project managers.

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

Job Summary:

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.

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

Education & Experience:

· 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

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

Quality Engineer II Salary: $78,375.00- $114,950

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.

U.S. Applicants: Equal Opportunity Employer. In addition, veterans and individuals with disabilities are encouraged to apply.

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