Quality Engineer 1, Manufacturing
Job
Cook Group
Bloomington, IN (In Person)
Full-Time
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Job Description
Quality Engineer 1, Manufacturing
Requisition ID
2026-18159
Posting Date
2 weeks ago
(3/19/2026 8:30 PM)
Job Location(s) Bloomington IN United States Job Locations US-IN-Bloomington Position Type Full Time Company Cook Inc - Bloomington Category Quality
Overview 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. Responsibilities
- 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 Qualifications
- Bachelors degree in a scientific discipline or equivalent experience
- Demonstrates knowledge of medical device regulation (ISO 13485, 21CFR) and risk management (ISO 14971)
- 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
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