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New · posted Oct 15

Cook Medical · Medical Devices

Quality Engineer 2, Manufacturing

  • Bloomington, IN
  • On-site
  • Full-time
  • Senior & Principal
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EmploymentFull-time
Deadline

Closes Mar 19, 2027 · 155 days left

The role

The Quality Engineer at Cook Inc. serves as the lead quality representative of certain product lines within product development, manufacturing, post-market surveillance, and/or CAPA.

What you need

• Bachelors degree in engineering

• Qualified candidates must be legally authorized to be employed in the United States. Cook does not intend to provide sponsorship for employment visa status (e.g., H-1B or TN status) for this employment position. • Demonstrates knowledge of medical device regulation (ISO 13485, 21CFR) and risk management (ISO 14971)

• 3-5 years of experience• Professional certification (e.g. ASQ, Six Sigma, etc.) preferred• Proficiency in statistical, quality and continuous improvement methods and tools

• Proficiency in the Microsoft Office suite of products (Word, Excel, PowerPoint, and Outlook) is required.• Strong organizational skills• Critical thinking and attention to detail required• Excellent verbal communication skills and technical writing

Physical Requirements

• Works under general office environmental conditions, including time in manufacturing environment and biohazard lab• Sitting for extended periods, utilizes close visual acuity for working with computers, equipment, etc.• Occasional travel may be required

What you'll do

• Perform work per external and internal quality standards• Interface with internal and external groups on quality-related issues• Support product development and transfer to manufacturing• Facilitate development and implementation of production controls (e.g. qualification, process capability, sampling plans, validation, etc.)• Perform investigation of product nonconformance/complaints, root cause analysis, monitoring/trending of process and product, and escalation of identified issues• Plan, review, and approve change requests• Execute risk assessment as needed and facilitate development and completion of risk file documentation• Conduct Risk-based decision making and effective resolution of issues• Lead or support CAPAs as necessary

• May interface with internal or 3rd party audits (e.g. FDA, Notified Body, etc.)• Drive continuous improvement efforts through facilitating, leading, and collaborating with cross function teams including quality, engineering, production, clinical, and regulatory affairs.• Provide leadership in the understanding of medical device regulations and best practices• Manage conflict resolution as it relates to technical situations• Must work and interact effectively and professionally with and for others throughout various levels of the organization• Must strictly adhere to safety requirements

Where you'll work

Bloomington, INOn-siteOpen in Maps (opens in a new tab)

More jobs in Bloomington, IN

Job intelligence

The context around this role

Live data · October 15, 2026

Salary intelligence

How the pay compares

Senior & Principal roles in Indiana13 roles publishing pay

Middle half $117,000 to $119,000, median $117,000

Senior & Principal roles in the US284 roles publishing pay

Middle half $103,375 to $137,500, median $122,750
Annual base pay
Annual base payLowMedianHigh
Indiana$117,000$117,000$119,000
All US$103,375$122,750$137,500

Comparisons: the base pay employers published on open Quality Assurance roles at the same level on Regulatory Jobs, October 15, 2026. Nothing is estimated.

Career trajectory

Where this role sits in Quality Assurance

The general path across 845 open Quality Assurance roles on Regulatory Jobs, with the titles they carry most. Not Cook Medical's own promotion track.

  1. One step back

    Associate & Specialist

    Often: Quality Engineer · Quality Technician

    $79K median227 open
  2. This role

    Senior & Principal

    Often: Quality Engineer · Senior Quality Engineer

    $123K median353 open
  3. Next step

    Manager

    Often: Manager, Quality Assurance · Quality Manager

    $153K median136 open
  4. Later

    Director

    Often: Director, Quality · Associate Director, Clinical Quality Assurance

    $209K median114 open
  5. Later

    VP & Executive

    Often: Vice President, Quality Assurance · AVP

    $302K median15 open

Skills DNA

What this role leans on

How many of the posting's 8 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.

GMP and compliance: 2 linesLab testing and methods: 1 lineDocumentation and SOPs: 2 linesInvestigations and CAPA: 2 linesValidation and qualification: 1 lineQuality systems and risk: 4 linesData and digital systems: 2 linesCollaboration and leadership: 4 linesGMPLab testingDocumentationInvestigationsValidationQuality systemsData systemsTeamwork
  • Quality systems and risk4
  • Collaboration and leadership4
  • GMP and compliance2
  • Documentation and SOPs2
  • Investigations and CAPA2
  • Data and digital systems2
  • Lab testing and methods1
  • Validation and qualification1

Company hiring pulse

Cook Medical on Regulatory Jobs

7
Open roles
6
Distinct roles
4
Locations

By discipline

  • Quality6 86%
  • Regulatory1 14%

By level

  • Senior & Principal4 57%
  • Associate & Specialist3 43%
See all 7 Cook Medical roles

More roles at Cook Medical

All 7 Cook Medical roles

Similar Quality Assurance roles elsewhere

Quality Engineer 2, Manufacturing at Cook Medical

Applications close March 19.

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    Quality Engineer 2, Manufacturing at Cook Medical — Bloomington, IN | Regulatory Jobs