Manufacturing Technician I - 10hr Monday to Thursday

Thermo Fisher Scientific•Logan, UT
•Onsite

About The Position

As part of Thermo Fisher Scientific’s Single Use Division in Logan, Utah, the Manufacturing Technician I manufactures, assembles, inspects, and packages Bioprocess Containers in a cleanroom environment. The technician follows Standard Operating Procedures (SOPs), Work Instruction Documents (WIDs), blueprints, and drawings for assembly, material handling, equipment operation, and finished-goods packaging, and participates in the site Technician Training Program. The role is fully on-site and follows a 10-hour first-shift schedule, 6:00 AM to 4:30 PM, Monday through Thursday. The work takes place in a temperature-controlled cleanroom and production environment, with required GMP and safety compliance, personal protective equipment, and strict cleanroom restrictions.

Requirements

  • High school diploma or equivalent.
  • No previous work experience required.
  • Competency using computers, Microsoft Office products, and inventory management systems.
  • Strong verbal and written communication skills.
  • Attention to detail and problem-solving abilities.
  • Ability to read and understand written materials, including words, pictures, and numbers.
  • Ability to count, sort, calculate, and measure accurately using tools such as calculators and tape measures.
  • Ability to understand chemical safety, including interpreting labels and Safety Data Sheets (SDS).
  • Ability to work in a fast-paced environment for up to 12 hours a day, with additional overtime as required.
  • Ability to stand and walk for a full shift and reach, bend, twist, stoop, push, and grasp while performing tasks.
  • Ability to use hand tools and equipment, including forceful gripping, grasping, pushing, pulling, and repetitive motion.
  • Ability to lift 50 pounds without assistance.
  • Ability to adhere to GMP and safety standards and comply with cleanroom restrictions and required PPE.

Nice To Haves

  • Previous work experience in a cGMP environment, manufacturing, operations, production, or warehouse.

Responsibilities

  • Manufacture, assemble, inspect, and package Bioprocess Containers according to SOPs, WIDs, blueprints, and drawings.
  • Operate production machinery and assemble tubing and connectors.
  • Handle materials and package finished goods.
  • Follow safety standards, current Good Manufacturing Practices (cGMP), company operating procedures, and policies.
  • Help ensure products meet quality standards by collaborating with other stations and departments to address quality errors.
  • Maintain accurate documentation while performing tasks.
  • Participate in Practical Process Improvements (PPI) activities.
  • Work effectively toward goals individually and as part of a team.
  • Complete required training on time and support personal development.
  • Follow the work schedule and meet department and site goals while maintaining quality.
  • Perform additional duties as assigned to support business and operational needs.

Benefits

  • Competitive pay.
  • Performance-related bonus where eligible.
  • Annual merit performance-based increase.
  • Medical, dental, and vision benefits effective Day 1.
  • Paid time off/annual leave.
  • Tuition reimbursement.
  • Employee referral bonus.
  • Career advancement opportunities.
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