MANUFACTURING TECHNICIAN I

Thermo Fisher Scientific•Lebanon, TN

3d•Onsite

About The Position

The Manufacturing Technician I works in Thermo Fisher Scientific’s Single Use Division at its Logan, Utah location. The role manufactures, assembles, and packages Bioprocess Containers in a cleanroom, following 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 and contribute to individual and team production goals while maintaining quality and safety standards. This is a fully on-site, 10-hour night-shift position, Monday through Thursday, from 6:00 p.m. to 5:00 a.m. The work includes frequent cleanroom entry, standing and walking for a full shift, and may require working up to 12 hours a day with additional overtime as needed. The cleanroom is temperature controlled and has restrictions on personal products and items such as jewelry, makeup, nail polish, perfume, piercings, lotion, and chewing gum. Required protective equipment may include safety-toed boots, high-visibility gear, safety glasses, cleanroom suit, hair or beard coverings, gloves, lab coat, and ear plugs. The position requires adherence to GMP and safety standards. Physical tasks include reaching, bending, twisting, stooping, pushing, grasping, repetitive motions, and lifting up to 50 pounds without assistance. The work environment may include loud equipment and machinery.

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.
Accurately count, sort, calculate, and measure using tools such as calculators and tape measures.
Ability to understand chemical safety, including interpreting labels and Safety Data Sheets (SDS).
Adhere to GMP and safety standards.
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.
Comply with cleanroom restrictions and wear required personal protective equipment.

Nice To Haves

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

Responsibilities

Operate equipment and perform production-related tasks, including assembling boxes and packaging and preparing finished products for shipment.
Assemble Bioprocess Containers in a cleanroom according to SOPs, WIDs, blueprints, and drawings.
Handle materials, operate equipment, and package finished goods.
Use computers, calculators, measuring tools, assembly hand tools, Bioprocess Container machinery, and pallet jacks.
Follow safety standards, cGMP requirements, company operating procedures, and policies.
Help ensure products meet quality standards and collaborate 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 training on time and focus on personal development.
Follow the work schedule to support department and site goals while maintaining quality.
Perform additional duties as assigned to support business and operational needs.