Assembly Production Technician I - 1st shift

Thermo Fisher Scientific•Logan, UT

1d•Onsite

About The Position

The Assembly Production Technician I works in Thermo Fisher Scientific’s Single Use Division at its Logan, Utah location. The role 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. This is a fully on-site production role in a temperature-controlled cleanroom. The work requires adherence to GMP and safety standards, use of required personal protective equipment, and compliance with restrictions on personal products and accessories in the cleanroom. The role involves working in a fast-paced environment for up to 12 hours a day, with additional overtime as required. Technicians must be able to stand and walk for a full shift, perform repetitive physical tasks, and lift up to 50 pounds without assistance.

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).
Adherence to GMP and safety standards and to cleanroom restrictions.
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 to 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 wear required PPE, including safety-toed boots, high-visibility gear, safety glasses, cleanroom suit, hair or beard coverings, gloves, lab coat, and ear plugs.

Nice To Haves

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

Responsibilities

Manufacture, assemble, inspect, and package Bioprocess Containers in a cleanroom environment.
Operate machinery and assemble tubing and connectors in accordance with blueprints and drawings.
Follow SOPs, WIDs, blueprints, drawings, cGMP requirements, safety standards, company procedures, and policies.
Handle materials, operate equipment, and package finished goods as directed.
Use computers, calculators, measuring tools, assembly hand tools, Bioprocess Container machinery, and pallet jacks.
Collaborate with other stations and departments to address quality errors and ensure products meet quality standards.
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 in a timely manner and focus on personal development.
Adhere to the work schedule and support department and site goals while maintaining quality.
Perform additional duties as assigned to support business and operational needs.