Process Controls Engineer (Manufacturing)

iMPact Business Group; Cary (IL); On-site; USD 57,859 - 63,369; Full time

Job summary

A leading technology firm in Cary, Illinois is looking for a Process Controls Engineer for a 12-month contract. The candidate must have a Bachelor's degree and at least 5 years of experience in quality processes, particularly in regulated industries such as medical devices. Responsibilities include developing process controls, integrating equipment capabilities, and vendor management. This role offers a competitive pay range and an opportunity to work in a collaborative environment.

Qualifications

• 5+ years of experience in quality process with external vendors.
• 4+ years experience in regulated environment like medical devices.
• Experience with PPAP and process validation.

Responsibilities

• Develop and modify process formulations and controls.
• Review product requirements for compatibility with methods.
• Integrate equipment capabilities to meet specifications.

Skills

Self Motivation

Task management

Knowledge of pFMEA

Risk Analysis

Process Control Plans

Project Management

Education

Bachelor's degree in science, engineering, or related subject

Master's Degree in science or engineering

Job description

Process Controls Engineer (Manufacturing)

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iMPact Business Group provided pay range

This range is provided by iMPact Business Group. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$42.00/hr - $46.00/hr

Our client, a Global Medical Device Manufacture has an immediate opening for a Process Controls Engineer for a 12 Month + Contract. Our client offers results-driven people a place where they can make a difference - every day! You will also have the opportunity to work with other like-minded, self-directed and detail oriented Top Talents in an extremely collaborative and professional environment.

Position Description (Principle Duties and Responsibilities)

• Develops and modifies process formulations, methods and controls to meet quality standards. Recommends and implements improvements, modifications or additions to document work.
• Reviews product development requirements for compatibility with processing methods to determine costs and schedules.
• Integrates equipment and material capabilities to meet process module target specifications and technology target specifications
• Job will require regulated industry experience and preferred medical device experience.
• Self Motivation and task management is expected
• Experience with PPAP, process validation, process development Program Management experience is an asset
• Project is electro-mechanical with embedded software - experience in these types of projects is required.
• Supply / Vendor Management will be a key responsibility

What you need

• Bachelor's degree in science, engineering, or related subject required.
• Master's Degree in science or engineering preferred
• Minimum of 5 years' experience in the area of quality process working closely with external vendors procuring parts and ensuring those parts meet specifications.
• Minimum of 4 years' experience in regulated environment (medical devices, automotive or aerospace) highly preferred.
• Strong knowledge and understanding of pFMEA, Risk Analysis and Process Control Plans is required.