Full-Time

Quality Engineer 2

Manufacturing

Deadline 3/19/27
Cook Group

Cook Group

5,001-10,000 employees

Medical devices for minimally invasive care

No salary listed

No H1B Sponsorship

Bloomington, IN, USA

In Person

Occasional travel may be required.

Bachelor's

Category
Manufacturing Quality & Test (1)
Required Skills
Microsoft Office
Word/Pages/Docs
Risk Management
Excel/Numbers/Sheets
Microsoft Outlook
PowerPoint/Keynote/Slides

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Requirements
  • A bachelor's degree in engineering is required.
  • The candidate must be legally authorized to work in the United States; the employer does not intend to provide employment visa sponsorship, including H-1B or TN sponsorship.
  • Demonstrated knowledge of medical device regulations, including ISO 13485 and 21 CFR, and risk management under ISO 14971.
  • Three to five years of experience is required.
  • Proficiency in statistical, quality, and continuous improvement methods and tools is required.
  • Proficiency in Microsoft Office, including Word, Excel, PowerPoint, and Outlook, is required.
  • Strong organizational skills, critical thinking, attention to detail, verbal communication, and technical writing skills are required.
  • The candidate must adhere strictly to safety requirements.
  • The candidate must be able to work under office conditions, in manufacturing environments, and in a biohazard laboratory; perform extended sitting and close visual work with computers and equipment.
Responsibilities
  • Serve as the lead quality representative for assigned product lines across product development, manufacturing, post-market surveillance, and/or corrective and preventive action activities.
  • Perform work according to 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, including qualification, process capability, sampling plans, and validation.
  • Investigate product nonconformances and complaints; perform root cause analysis, process and product monitoring and trending, and escalation of identified issues.
  • Plan, review, and approve change requests.
  • Execute risk assessments and facilitate development and completion of risk-file documentation.
  • Apply risk-based decision-making and resolve issues effectively.
  • Lead or support corrective and preventive actions as necessary.
  • Interface with internal or third-party audits, including FDA and notified-body audits.
  • Drive continuous improvement by facilitating, leading, and collaborating with cross-functional teams in quality, engineering, production, clinical, and regulatory affairs.
  • Provide leadership in understanding medical device regulations and best practices.
  • Manage conflict resolution related to technical situations.
  • Interact effectively and professionally with people throughout various levels of the organization.
Desired Qualifications
  • Professional certification, such as ASQ or Six Sigma, is preferred.
  • Occasional travel may be required.

Cook Group develops and manufactures medical devices, focusing on minimally invasive technologies that help hospitals perform procedures without open surgery. Its products, from catheters and wire guides to a broad range of specialized devices, are designed to be used in interventional procedures across cardiology, urology, gastroenterology, and more. The company differentiates itself through long-term, family-owned leadership and a vast portfolio of over 16,000 products, with a global reach to about 135 countries and strong clinical support for clinicians. Its goal is to provide reliable technologies and services that advance minimally invasive care and improve patient outcomes.

Company Size

5,001-10,000

Company Stage

N/A

Total Funding

N/A

Headquarters

Paris, France

Founded

1963

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Simplify Jobs

Simplify's Take

What believers are saying

  • September 2, 2026 emissions target cuts scope 1 and 2 greenhouse gases 35% by 2035.
  • June 2026 launches of Volante and SureTome expanded U.S. and Canadian endoscopy revenues.
  • Canadian system modernization went live July 2, 2026, improving ordering and billing accuracy.

What critics are saying

  • FDA classified Cook's sizing catheter recall as Class I on May 5, 2026.
  • August 2026 FDA recalls show process-control failures across wire guides and liver access sets.
  • MDL 2570's 6,537 pending IVC filter cases threaten Cook's core implant franchise.

What makes Cook Group unique

  • Cook Medical's 16,000-product portfolio spans cardiology, urology, and gastroenterology across 135 countries.
  • The Cook family still owns it, enabling patient-first capital allocation over quarterly pressure.
  • Siemens partnership on SIR 2026 positions Cook in image-guided interventional MRI procedures.

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Benefits

Health Insurance

Dental Insurance

Vision Insurance

401(k) Retirement Plan

401(k) Company Match

Paid Vacation

Paid Holidays

Paid Sick Leave

Parental Leave

Hybrid Work Options

Company News

Medical Buyer
Jan 6th, 2025
Endoscopic closure devices market to grow by USD 825.7 million

For instance, Cook Group, a leading vendor, introduced the Instinct Endoscopic Hemoclip.

Cook Group
Jan 8th, 2024
Cook Group announces sale of West Lafayette's Cook Biotech to RTI Surgical

Bloomington, Ind. - In the latest of a series of strategic decisions aligned to its 5-year vision, Cook Group announced today that RTI Surgical will acquire Cook Biotech, a Cook life sciences company based in West Lafayette, Ind.

Indiana Public Media
Jan 8th, 2024
Cook Group selling off biotech company in West Lafayette

The Cook Group is selling Cook Biotech, a life sciences company based in West Lafayette, to RTI Surgical.

CFC Properties
Jan 6th, 2023
Jim Murphy retiring from CFC Properties after 35 years; Ron Walker promoted to president

Cook Group announced today that Jim Murphy will be retiring from his role as president of CFC Properties in May 2023 after 35 years of service.