Manufacturing Engineer — Medical Device; Onsite — Arden Hills, MN Temp

Saint Paul, United States | Posted on 06/19/2026

Job Summary:

The day‑to‑day responsibilities of this role center around supporting manufacturing operations. The Manufacturing Engineer I will provide daily manufacturing support by reviewing prior‑day performance signals related to yield, labor, and throughput. The candidate will participate in daily morning meetings to review current priorities, receive action items, and execute assigned tasks throughout the day. This role will own assigned manufacturing stations, equipment, and associated processes, ensuring that equipment is functioning as intended, processes remain stable and controlled, and yields consistently meet established performance expectations.

The business sets defined yield thresholds, and the engineer will be responsible for maintaining performance at or above these thresholds while also supporting continuous improvement initiatives achieving stretch goals. A successful Manufacturing Engineer I on this team demonstrates strong communication and reliability, effectively managing daily responsibilities while keeping stakeholders informed. Under supervisory direction, the role assists in the daily support of products, processes, materials, and equipment to achieve production goals (quality, delivery, cost, productivity, safety).

• Works cooperatively with R&D, Process Development, Quality, Production, Regulatory, Equipment Engineering, Supply Chain, and Marketing to ensure project success.
• Identifies and implements improvements (e.g., yields, processes, and productivity).
• Undertakes and successfully completes simple or basic product support tasks such as verifying specifications, maintaining product/process documentation, testing processes, equipment, raw materials and product, and validating equipment processes.
• Assists in inventing/creating concepts and designs/approaches for new processes/test methods.
• Designs, procures, and fabricates basic equipment tooling and fixtures.
• Designs and coordinates rudimentary engineering tests and experiments.
• Summarizes, analyzes, and provides recommendations from test results.
• Performs troubleshooting on existing products/process problems as related to design, material, or processes.
• Prepares standard reports/documentation to communicate results to the technical community.
• Assists in identification and implementation of production goals.
• Trains operators/technicians on new processes and/or test procedures.

Build quality into all aspects of the work by maintaining compliance to all quality requirements.

• 0–1 year experience with a BS in engineering field.
• Driven / Self‑motivated – takes initiative to identify issues and pursue solutions.
• Effective communication – able to elevate issues when needed, engage the appropriate cross‑functional partners, and clearly articulate actions being taken.
• Collaboration skills – works effectively with other engineers and cross‑functional teams to develop and implement solutions.
• Execution & follow‑through – focused on completing assigned tasks, proactively communicating status and delays when timelines are impacted.
• Problem‑solving ability – capable of defining problems and working through potential working theories.

• Medical device experience/exposure (OQ, PQ, PMV).

• Schedule:
  
  08:00 AM – 04:30 PM
• Work setup:
  Onsite – Arden Hills, MN
• Contract duration: 6 months (7/20/2026 – 1/19/2027); possible temp‑to‑hire.

Pharmavise Corporation is an Equal Opportunity Employer and does not discriminate on the basis of race or ethnicity, religion, sex, national origin, age, veteran disability or genetic information or any other reason prohibited by law in employment.