Manufacturing Technician 1

Thermo Fisher Scientific • Logan, UT

1d • Onsite

About The Position

As a Production Technician I at Thermo Fisher Scientific, you will manufacture, assemble, inspect, and package Bioprocess Containers in a cleanroom environment. You will safely follow Standard Operating Procedures (SOPs), Work Instruction Documents (WIDs), blueprints, and drawings covering assembly, material handling, equipment operation, and finished-goods packaging. You will also progress through the site Technician Training Program.

The role is fully onsite in a temperature-controlled cleanroom and involves operating machinery, assembling tubing and connectors, using tools and equipment, maintaining accurate documentation, and working with other stations and departments to address quality issues. You will follow GMP and safety requirements, participate in Practical Process Improvements (PPI), work toward individual and team goals, complete training, and support business and operational needs. The position requires working in a fast-paced environment for shifts of up to 12 hours, with additional overtime as required.

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).
• Adhere to Good Manufacturing Practices and safety standards.
• Ability to work onsite in a cleanroom and comply with its restrictions on personal products and accessories.
• 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 work around loud equipment and machinery noise.

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.
• Follow SOPs, WIDs, blueprints, drawings, cGMP requirements, safety standards, company procedures, and policies.
• Operate machinery and assemble tubing and connectors.
• Handle materials and package finished goods.
• 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 training in a timely manner and focus on personal development.
• Adhere to the work schedule 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.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Education Level: High school or GED