Senior Manufacturing Support Technician (Utah)

Hydrogen UK Ltd; Draper (UT); On-site; USD 64,472,000 - 75,823,000; Full time

Job summary

Hydrogen UK Ltd in Draper, UT is seeking a Technician for a 1-year W2 contract in a medical device manufacturing setting. The role centers on setting up feasibility studies, running tests, and following protocols to validate and improve equipment and processes.

Responsibilities include collaborating with Engineers and Technicians, updating ERP/MRP documentation, and developing training materials to share knowledge across projects while adhering to EH&S and quality guidelines.

Qualifications

• H.S. Diploma or equivalent.
• 2-4 years of experience required.

Responsibilities

• Consult with Engineers, Technicians, and Assemblers on processes to execute experiments and/or production runs.
• Review documentation and ensure information is catalogued and transferred for Engineering approval.
• Utilize manufacturing software (e.g., JDE, QMS, PLM) to update documentation in systems.
• Develop training and documentation materials with Engineering collaborations to enable knowledge transfer.
• Lead projects related to new equipment validation, investigations, testing, and rework.

Skills

MS Office

English communication

QA/QC guidelines

Documentation practices

Troubleshooting equipment

Process validation

Team collaboration

Project coordination

Education

High School Diploma

Tools

JDE

QMS

PLM

Job description

Location: Draper, UT (Onsite)

Schedule: Standard

Duration: 1-Year Contract (W2)

Pay Rate: $22.50 - $26.50/hr

Position Summary

Our client is a medical device manufacturer with clean room production operations. The main function of this technician role is to set up and execute feasibility studies, experiments, and tests - both creating and following established protocols - to develop findings for the validation and improvement of equipment and manufacturing processes/methods based on engineering principles. This role analyzes results, makes recommendations, and develops reports for Engineering review, and operates a variety of test equipment to assess characteristics of the manufacturing environment.

Essential Functions and Responsibilities

• Consult with Engineers, Technicians, and Assemblers on processes to execute experiments and/or production runs. Support related to equipment investigations, testing, objective evidence of product dispositions, and rework support work necessary.
• Review documentation and take appropriate actions to ensure that information is appropriately catalogued and follow through to validation and qualification of equipment, including transferring information to appropriate locations (e.g., ECRs, SOPs, drawings, and tooling) for Engineering approval.
• Utilize manufacturing software (e.g., JDE, QMS, PLM) to update documentation in systems.
• Follow through with development of training and documentation materials, based on collaboration with Engineering, including identifying opportunities for modification and making recommendations, enabling the seamless knowledge transfer of project and manufacturing processes; applying knowledge of processes to devise process changes in collaboration with Engineering.
• May lead projects related to new equipment validation, equipment investigations, testing, objective evidence of product dispositions, and rework.
• Identify potential improvement opportunities and propose solutions to optimize process and/or equipment (e.g., re-design/design of basic equipment, tools, fixtures, etc.) to improve manufacturing processes, for Engineering review.
• Provide coaching and guidance to technicians.

Education/Experience

• H.S. Diploma or equivalent
• 2-4 years of experience required

Knowledge/Skills

• Excellent computer skills required, including experience with MS Office Suite; ERP/MRP systems experience preferred
• Ability to read, comprehend, write and speak English, and good communication skills required
• Knowledge of and adherence to the client's Environmental Health and Safety and Quality guidelines as they relate to department clean room medical device manufacturing
• Knowledge of Good Manufacturing and Good Documentation Practices supporting a medical device environment
• Strict attention to detail
• Ability to provide feedback in a professional, direct, and tactful manner
• Must be able to work in a team environment and with minimum supervision
• Proven success adhering to project schedules and managing small projects
• Substantial knowledge of validation and improvement of automated equipment
• Ability to troubleshoot manufacturing equipment
• Knowledge of material compatibility in the proposed use environment