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Added 3 mins ago
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Quality Process Engineer
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- $85,000 to $115,000 USD / year
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GPAC

Quality Process Engineer

Colebrook, CT, United States

$85,000 to $115,000 USD / year

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Job details

Pay: $85,000 to $115,000 USD / year
Apply by: Jan 28, 2027
Posting language: English
Posted: Oct 30, 2026

Original job description

Process Engineer – Quality Focus

Position Summary

The Process Engineer – Quality Focus is responsible for developing, validating, controlling, and continuously improving manufacturing processes, with an emphasis on process capability, product quality, and long-term process robustness within a regulated medical device manufacturing environment.

This role serves as the technical owner of injection molding and secondary manufacturing processes, ensuring processes are capable, compliant, sustainable, and aligned with internal quality standards, customer requirements, and regulatory expectations. The Process Engineer partners closely with Quality, Production, Tooling, Maintenance, Engineering, and Program Management teams to support daily manufacturing operations, new product introductions, and continuous improvement initiatives.

Essential Duties and Responsibilities

Process Ownership & Control

• Develop, establish, optimize, and maintain robust manufacturing processes for plastic injection molding and secondary operations.

• Serve as the process owner for assigned manufacturing cells and production lines.

• Define and maintain critical process parameters, validated process windows, and process control strategies to ensure consistent product quality and process stability.

• Monitor process performance utilizing SPC, capability analysis, and other statistical tools; respond appropriately to trends, variation, and out-of-control conditions.

• Troubleshoot molding and manufacturing process issues to improve efficiency, reduce variation, and minimize downtime.

• Support the establishment of standard process settings, setup instructions, and manufacturing best practices.

Process Validation & Technical Documentation

• Lead and execute process validations, including IQ, OQ, and PQ activities, for new and existing products in compliance with applicable medical device regulations and internal procedures.

•

Develop, review, and maintain technical manufacturing documentation, including:

• Process Flow Diagrams

• Process FMEAs (pFMEAs)

• Control Plans

• Work Instructions and Setup Standards

• Validation Protocols and Reports

• Ensure validation activities support long-term process capability and sustained manufacturing performance.

• Support change control activities related to materials, tooling, equipment, and process changes.

For immediate consideration, resumes can be sent to Thane Meiners with gpac. Email: thane.meiners@gogpac.com

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More about this job

Skills

Manufacturing processes
Program management
Process improvement
Control engineering
SPC
Troubleshoot
Documentation
SAP IQ
Regulatory compliance
Medical device regulations

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