Manufacturing Engineer

Katalyst Healthcares & Life Sciences; Utah; On-site; USD 60,000 - 75,000; Full time

Job summary

Katalyst Healthcares & Life Sciences is seeking an early-career engineer to join the manufacturing team supporting engineering and production activities for an active product development program. This role emphasizes hands‑on manufacturing support, documentation management, and collaboration with cross‑functional teams in a regulated medical device environment.

You will assist with change control, maintain manufacturing and engineering records, participate in builds, and help with investigations

Qualifications

• 1–4 years of experience in the medical device industry (Class II or III).
• Experience supporting manufacturing, quality, or engineering activities in a regulated environment.
• Exposure to documentation control, change control processes, manufacturing records, or related engineering documentation.

Responsibilities

• Support change control activities.
• Maintain manufacturing and engineering documentation.
• Assist with investigations and troubleshooting efforts.
• Participate in manufacturing builds.
• Execute studies designed by senior engineers.

Skills

Regulated environment

Documentation control

Change control

Manufacturing support

Medical device industry

Education

Engineering degree

Job description

Role Overview:

Our client is looking for someone to join the manufacturing team supporting engineering and production activities for an active product development program. This position is ideal for an early-career engineer who enjoys hands‑on manufacturing support, documentation management, and collaboration with cross‑functional teams. Responsibilities include supporting change control activities, maintaining manufacturing and engineering documentation, assisting with investigations and troubleshooting efforts, participating in manufacturing builds, and executing studies designed by senior engineers. The role provides strong mentorship and development opportunities while offering direct exposure to production operations and regulated medical device environments.

Required Skills:

• 1–4 years of experience within the medical device industry (Class II or Class III devices).
• Experience supporting manufacturing, quality, or engineering activities in a regulated environment.
• Exposure to documentation control, change control processes, manufacturing records, or related engineering documentation.

Nice to Have:

• Class III medical device experience.
• Experience supporting investigations, process studies, or data analysis activities.
• Hands‑on collaboration with manufacturing operators or production teams.
• Education: Engineering degree required.