Associate Engineering Technician

GForce Life Sciences; Salt Lake City (UT); Sur place; USD 30 000 - 41 000; Plein temps

Résumé du poste

GForce Life Sciences seeks an Associate Engineering Technician for an onsite contract role in Salt Lake City, UT. You will support engineering teams with prototype assembly, testing, and process documentation within a clean room environment.

Responsibilities include assembling prototypes, testing per instructions, and coordinating with project engineers, while ensuring adherence to GLP and QS standards. Two-year technical degree or equivalent experience preferred.

Qualifications

• Experience designing fixtures and tooling for prototyping, with hands-on skills.
• Experience working with external vendors.
• Strong analytical and problem-solving skills.
• Ability to apply high-quality standards consistently.
• Ability to multi-task effectively.

Responsabilités

• Assemble prototypes and products according to design plans.
• Test prototypes per engineering instructions and document results.
• Assist engineering teams in sourcing supplies and services.
• Communicate assignment status to project engineers.
• Train team members on new product processes and procedures.
• Ensure work complies with quality requirements, including GLP & QS standards.
• Verify products are tested using validated methods and all documentation is completed.

Connaissances

Fixture design

Vendor management

Analytical thinking

Quality standards

Multitasking

Formation

Two-year technical degree

Description du poste

Our client, a medical device company, has engaged GForce Life Sciences to provide an Associate Engineering Technician. This contract role will be based onsite at their facility in Salt Lake City, UT. The position supports engineering teams in prototype assembly, testing, and process documentation within a clean room environment.

Responsibilities

• Assemble prototypes and products according to design plans.
• Test prototypes in accordance with engineering instructions and document results.
• Assist engineering teams in sourcing supplies and services.
• Communicate assignment status to project engineers.
• Train team members on new product processes and procedures.
• Ensure work is conducted in compliance with all quality requirements, including GLP & QS standards.
• Verify that products are tested using validated methods and all documentation is accurately completed.

Mandatory Requirements

• Experience designing fixtures and tooling for prototyping, with emphasis on hands‑on skills.
• Experience working with external vendors.
• Strong analytical and problem‑solving skills.
• Ability to apply high‑quality standards consistently.
• Ability to multi‑task effectively.
• Two‑year technical degree (e.g., AA, Certificate) or equivalent experience.

Nice to Have

• 2+ years of technical work experience in medical device development