Manufacturing Technician I - 10hr Monday to Thursday

Thermo Fisher Scientific•Logan, UT

6d•Onsite

About The Position

As part of Thermo Fisher Scientific’s Single Use Division in Logan, Utah, the Manufacturing Technician I manufactures, assembles, and packages Bioprocess Containers in a cleanroom environment. The role follows Standard Operating Procedures (SOPs), Work Instruction Documents (WIDs), blueprints, and drawings for assembly, material handling, equipment operation, and finished-goods packaging. Technicians participate in the site Technician Training Program. The position is fully on-site and follows a 10-hour day schedule, 6:00 AM to 4:30 PM, Monday through Thursday. Work takes place in a temperature-controlled cleanroom with restrictions on personal products and accessories, and requires use of personal protective equipment. The role involves standing and walking throughout the shift, using tools and machinery, and lifting up to 50 pounds without assistance. Work may take place in a loud, fast-paced environment, with shifts of up to 12 hours and additional overtime as required.

Requirements

High school diploma or equivalent.
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.
Adherence to Good Manufacturing Practices and safety standards.
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 comply with cleanroom restrictions and wear required personal protective equipment.

Nice To Haves

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

Responsibilities

Operate machinery, assemble tubing and connectors, and package and inspect products according to blueprints and drawings.
Use computers, calculators, measuring tools, assembly hand tools, Bioprocess Container machinery, and pallet jacks.
Follow safety standards, current Good Manufacturing Practices (cGMP), company operating procedures, and policies.
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 to meet goals individually and as part of a team.
Complete training in a timely manner and focus on personal development.
Adhere to the work schedule and support department and site goals while maintaining work quality.
Perform additional duties as assigned to support business and operational needs.