Medical Device Process Development Engineer (R&D)

Actalent; Minnetonka (MN); On-site; USD 51,000 - 52,000; Full time

Benefits offered by this job

Medical, dental & vision

401(k) plan

Life Insurance

Disability insurance

Health Savings Account

Transportation benefits

Employee Assistance Program

PTO & vacation

Job summary

Actalent in Minnetonka, MN is hiring a Process Development Engineer (R&D - Medical Device) to advance manufacturing processes. You will author validations (TMV, IMV, IQ, OQ, PQ, PPQ), define development equipment specs, and drive continuous improvement with data-driven experiments.

The role requires 1–3 years in process development or related engineering within medical devices, hands-on manufacturing experience, and strong documentation and teamwork skills.

Qualifications

• 1–3 years in process development or related engineering in medical devices.
• Hands-on experience in medical device manufacturing or development.
• Proficient in authoring and executing process validations (TMV/IMV/IQ/OQ/PQ/PPQ).
• Strong engineering fundamentals and data-driven problem solving.
• Experience designing experiments and analyzing validation data.

Responsibilities

• Author and execute process validations (TMV/IMV/IQ/OQ/PQ/PPQ).
• Define specs for development equipment and lead new equipment acquisition.
• Apply engineering principles to solve process-related problems in medical devices.
• Design experiments, run validation tests, and analyze data for improvement.
• Prepare data and recommendations for equipment teams and stakeholders.
• Collaborate with engineers/technicians for solutions and cross-functional support.
• Train teams on process development and validation activities.

Skills

1–3 years process development

Hands-on medical device

Process validations (TMV/IMV/IQ/OQ/PQ/

Education

Bachelor's degree in engineering

Tools

Validation frameworks

Job description

Actalent in Minnetonka, MN is hiring a Process Development Engineer (R&D - Medical Device) to advance manufacturing processes. You will author validations (TMV, IMV, IQ, OQ, PQ, PPQ), define development equipment specs, and drive continuous improvement with data-driven experiments.

The role requires 1–3 years in process development or related engineering within medical devices, hands-on manufacturing experience, and strong documentation and teamwork skills.