Assembly Production Technician I - Weekend Days

Thermo Fisher Scientific•Logan, UT

3d•Onsite

About The Position

As part of the Thermo Fisher Scientific team, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world's toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer. This role is in the Single Use Division and will be performed at our Logan, Utah location. How You Will Make an Impact: As a Production Technician I, you will manufacture, assemble, and package Bioprocess Containers in a cleanroom environment. You will safely carry out the production process by closely following the Standard Operating Procedures (SOP), Work Instruction Documents (WID), blueprints, and drawings as they relate to assembly, material handling, equipment operation, and finished goods packaging. Production Technician I’s will work through the site Technician Training Program. Day in the Life: Work in a production environment where you will operate machinery, assemble tubing and connectors, and package and inspect products in accordance with blueprints and drawings. Use various tools and equipment, including computers, calculators, measuring tools, assembly hand tools, Bioprocess Container machinery, and pallet jacks. Follow safety standards, Current Good Manufacturing Practices (cGMP) requirements, company operating procedures, and policies. Ensure products meet quality standards by collaborating with other stations and departments to address quality errors. Maintain accurate documentation as the task is being performed. Participate in Practical Process Improvements (PPI) activities. Work effectively to consistently meet goals as an individual and as part of a team. Focus on personal development through timely completion of training. Adhere to schedule to meet department and site goals while maintaining focus on quality of work. Perform additional duties as assigned to support business and operational needs.

Requirements

High school diploma or equivalent.
No previous work experience required.
Competency in using computers, Microsoft Office products, and inventory management systems.
Strong verbal and written communication skills.
Attention to detail and problem-solving abilities.
Read and understand written materials, including words, pictures, and numbers.
Accurate counting, sorting, calculating, and measuring using tools like calculators and tape measures.
Ability to understand chemical safety, including interpreting labels and Safety Data Sheets (SDS).
Ability to stand and walk for full shift, 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.
Able to lift 50 pounds without assistance.

Nice To Haves

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

Responsibilities

Manufacture, assemble, and package Bioprocess Containers in a cleanroom environment.
Safely carry out the production process by closely following the Standard Operating Procedures (SOP), Work Instruction Documents (WID), blueprints, and drawings as they relate to assembly, material handling, equipment operation, and finished goods packaging.
Operate machinery, assemble tubing and connectors, and package and inspect products in accordance with blueprints and drawings.
Use various tools and equipment, including computers, calculators, measuring tools, assembly hand tools, Bioprocess Container machinery, and pallet jacks.
Follow safety standards, Current Good Manufacturing Practices (cGMP) requirements, company operating procedures, and policies.
Ensure products meet quality standards by collaborating with other stations and departments to address quality errors.
Maintain accurate documentation as the task is being performed.
Participate in Practical Process Improvements (PPI) activities.
Work effectively to consistently meet goals as an individual and as part of a team.
Focus on personal development through timely completion of training.
Adhere to schedule to meet department and site goals while maintaining focus on quality of work.
Perform additional duties as assigned to support business and operational needs.