Process Engineer, Medical Devices

GForce Life Sciences • cary, il, us • 1m ago

Process Engineer

12-month contract

Onsite in Cary, IL

Responsibilities:

Develop and refine process formulations, manufacturing methods, and quality controls to ensure compliance with industry regulations and company standards.
Identify, recommend, and implement process improvements, modifications, and documentation updates to enhance efficiency, consistency, and product quality.
Review product development requirements to evaluate compatibility with current processing methods, cost implications, and scheduling constraints.
Integrate equipment and material capabilities into production workflows to meet process module and technology target specifications.
Conduct root cause analysis and troubleshooting for process deviations, ensuring timely resolution and continuous improvement.
Collaborate with cross-functional teams, including R&D, quality, and manufacturing, to ensure seamless product development and commercialization.
Maintain accurate technical documentation and contribute to process validation efforts.

Qualifications & Requirements:

Bachelor’s degree in Engineering (Mechanical, Biomedical, Industrial, or related field) or equivalent practical experience.
Minimum of 2 years of experience in process engineering, preferably in a medical device or regulated manufacturing environment.
Strong understanding of process validation, quality systems, and regulatory requirements (ISO 13485, FDA, GMP, etc.).

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