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Principal Supplier Quality Engineer

Integer Holdings · Chaska, MN

Level
Senior
Team
Quality
Base pay
$144k–$211k
Experience asked
10+ years
Industry
Medical devices
Posted
3 days ago

The role in 30 seconds

A senior quality role at Integer Holdings (medical devices) in Chaska, MN. As well, you will serve as a coach and mentor for other engineers, modeling the behaviors and disciplines of an engineering or technical professional.

They ask for
10+ years
Tools it names
Root cause, FMEA, DOE, FDA / GMP, Validation (IQ/OQ/PQ), Supplier quality
Base pay
$144k–$211k

Read from the posting. The full description is below.

It asks for 10+ years. If you're close, apply anyway: requirements are a wish list. Talk to someone on the team first.

At a glance

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How to get in at this plant

Five moves over a week or two. The first one takes ten minutes.

  1. 1

    Pick 2–3 people on the Quality team at Integer Holdings

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  2. 2

    Send a short, curious note

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  3. 3

    Turn a reply into a short call

    Questions worth asking about this team:

    • What does a normal week look like on your team?
    • Which standards drive the work here: ISO 13485, IATF 16949, AS9100?
    • How much of the job is customer complaints versus prevention?
    • How did you land the job? What stood out in your interviews?
  4. 4

    Apply with someone vouching for you

    If the call went well, ask whether they’d pass your résumé to the hiring manager. Send your résumé link, apply that day, and let them know.

  5. 5

    Bring proof to the interview

    One page of before-and-after numbers from projects you led: scrap, OEE, cycle time, cost. Plant managers hire on results.

About the role

What you’ll do in this role

The primary purpose of this position is to provide strategic quality guidance that supports Integer’s goals. You will be applying intensive and diversifies quality knowledge and principles in extensive assignments and project leadership. As the authority in your field, you will provide guidance and quality leadership to others across Integer. The following are the expectations for this role:

  • ◆Apply intensive and diversified knowledge of engineering principles and practices in broad areas of assignments and related fields.
  • ◆Ensure Integer internal and external customer expectations are met or exceeded. Identifies and evaluates procedures to ensure the production of quality product.
  • ◆Develop new and unique approaches to complex problems and can advance technology beyond previous achieved levels.
  • ◆Apply engineering concepts to resolve acute or chronic problems.
  • ◆Conduct studies to understand capability for process and/or measurement systems. Provides management with technical guidance as required.
  • ◆Identify and develop appropriate documentation for process improvement and project implementation.
  • ◆Maintain liaison with individuals and units within or outside the organization with responsibility for acting independently on technical matters pertaining to their filed.
  • ◆You adhere to Integer’s Values and all safety, environmental, security and quality

requirements

including, but not limited to: Quality Management Systems (QMS), Safety, Environmental and Security Management Systems, U.S. Food and Drug Administration (FDA) regulations, company policies and operating procedures, and other regulatory requirements.

Specific Supplier Quality

responsibilities

  • ◆You will manage supplier non-conformances, liaising with suppliers to ensure all issues are adequately addressed
  • ◆You will manage and conduct supplier audits, tracking the closure of any audit related findings.
  • ◆You will lead the suppliers’ product and process change notification system, as applicable
  • ◆You will lead Supplier Quality Agreement management process with suppliers.
  • ◆You will work with Suppliers, Management, Supply Chain, Engineers and Manufacturing associates in the resolution of supplier quality problems. Also, assist each of these groups with capability studies and the application of statistical quality control which include Cpk, DOE, Hypotheses Testing, etc.
  • ◆You will be responsible for managing the sourced item qualification process and ensuring all appropriate documentation is completed.
  • ◆You will be responsible for managing the First Article Inspection process.
  • ◆You will monitor supplier related KPIs, assuring compliance with DMR while providing deviation/waiver guidance and assuring complete and correct Device History Records are maintained.
  • ◆You will review the adequacy and correctness of changes to Bill of Materials (BOM’s), Incoming Inspection Plans, Drawings, Component Specification, FMEAs, etc.
  • ◆You will be supplier quality resource for any site continuous improvement projects.
  • ◆You will support product transfers.
  • ◆You may provide supervision for up to 3 engineering direct reports. As well, you will serve as a coach and mentor for other engineers, modeling the behaviors and disciplines of an engineering or technical professional.
  • ◆You will perform work on technical projects where you will follow Integer’s standard quality management and production system methodologies to investigate opportunities for product and process improvements.
  • ◆You are expected to collaborate with others in the exchange of information, ask questions and regularly check for understanding in support of your development as an engineer.
Show full description ↓

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

Who are we?

Integer is a global organization providing innovative, high-quality technologies and manufacturing to Medical Device OEM’s (original equipment manufacturers) to enhance the lives of patients worldwide. We are guided by our six Values, including focus on Customers, Innovation, Collaboration, Inclusion, Candor, and Integrity. Working at Integer means you are part of a team passionately pursuing excellence in all that we do and always reaching for the next great achievement.

Support Non-Conforming Material Process

  • •You will ensure that the disposition of supplier caused non-conforming materials meet all necessary procedures and assure adequacy of supplier corrective actions to prevent re-occurrence.
  • •You will lead site SCAR activities, including analysis of data and trends in supplier quality nonconforming material, bounding and containment, root cause analysis and effectiveness verification.

Support Site Quality Activities

  • •You will support and lead internal quality audit activities, as applicable
  • •You will support regulatory and agency inspections, audits, investigations, and inquiries related to supplier quality.
  • •You embed Quality– “I own Quality.” You are a standard bearer for Quality in everything we do at Integer, by assuring adherence to our Quality Management System (QMS), supporting to corrective and preventive actions investigation and implementation, and contributing to the successful attainment of our quality KPI’s and journey to 5 Sigma.
  • •You may perform other duties as needed and as directed by your line of supervision.

Support Integer’s Manufacturing Excellence and Market Focused Innovation Strategies

  • •Strategy Alignment through Site Hoshin Plans, Quality Plans, Validation master plans, associated

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