Process Engineer III

Riverpoint Medical; Portland (OR); On-site; USD 80,000 - 110,000; Full time

Job summary

Riverpoint Medical is seeking a Process Engineer III to enhance internal systems and processes in the medical device industry. The role involves collaboration with various teams, project management, and ensuring compliance with quality standards. Ideal candidates will have a relevant engineering degree and substantial experience in medical device development, including familiarity with FDA regulations.

Benefits

Medical Insurance

Dental Insurance

Vision Insurance

Life Insurance

401(k) with company match

Paid Time Off

Holidays

Qualifications

• 4-10 years of experience in medical device development.
• Experience with FDA regulations and equipment validation.
• Background in LEAN manufacturing or GMP.

Responsibilities

• Drive improvements to internal systems and equipment validations.
• Collaborate with teams to develop process solutions.
• Manage projects supporting strategic goals.

Skills

Project Management

Collaboration

Process Improvement

Quality Compliance

Education

Bachelor’s degree in Engineering

Graduate degree preferred

Job description

Join to apply for the Process Engineer III role at Riverpoint Medical.

Riverpoint Medical, located in Portland, Oregon, is seeking a Process Engineer III. Our company specializes in designing and manufacturing premium medical devices for Medical, Dental, and Veterinary markets, including suture technologies, sports medicine fibers and anchors, surgical lighting, and needle technologies.

Responsibilities include:

1. Driving proactive improvements to internal systems, processes, and equipment validations.
2. Collaborating with Operations, NPD, Quality, and Regulatory teams to develop robust process solutions.
3. Managing projects supporting the company's strategic goals and implementing ECO processes.
4. Organizing project elements, coordinating teams, and ensuring compliance with quality standards.
5. Supporting documentation, labeling, and ERP functions for new product transfers.
6. Supporting company initiatives related to QMS, EMS, and regulatory requirements.

Qualifications:

1. Bachelor’s degree or equivalent in Mechanical, Materials Science, Chemical, Electrical, or Biomedical Engineering; graduate degree preferred.
2. 4-10 years of experience in medical device development, manufacturing, or reprocessing.
3. Experience with FDA regulations, including 510(k) submissions, and equipment/process validation (IQ/OQ/PQ).
4. Background in LEAN manufacturing, GMP, or NPD. Experience in sterilization, sealing, or packaging is a plus.

We offer excellent benefits, including Medical, Dental, Vision, Life Insurance, 401(k) with company match, Paid Time Off, and holidays.

Riverpoint Medical is an equal opportunity employer committed to diversity and inclusion.