Production Support Technician I

Thermo Fisher Scientific•St. Louis, MO

1d•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. Location/Division Specific Information: (Equipment Cleaning/Assembly) St. Louis, MO/ Drug Substance Division (Biologics) Work Schedule 12-hour shift working the 2-2-3 rotating schedule Day Shift is 6:00am to 6:30pm How Will You Make an Impact? The candidate will be responsible for cleaning and sanitizing primary, secondary, and ancillary equipment using industrial washers and Clean out of Place stations. Responsibilities additionally include assembling manufacturing tanks, vessels, and line assemblies to support the manufacture of commercial and clinical biologics. Additional activities consist of, but are not limited to, the formulation of cleaning solutions, visual inspections of equipment, and the operation of autoclaves in compliance with standard cGMP practices including documentation.

Requirements

High school diploma or equivalent required.
No previous work experience required
Able to read, write, and communicate in English
Able to work in an environment of change independently and as part of a team
Be willing to wear a full gowning suit which includes bodysuit, gloves, hair & beard nets, face covers, and safety glasses. (These items are prohibited: makeup, jewelry, nail polish, cologne / perfume, scented lotions, or hair care products, etc.)
Able to adhere to clean room gowning requirements, including wearing Tyvek, Nitrile, and/or Latex gloves
Ability to lift minimum of 25 lbs. independently
Ability to stand, walk, reach, stoop, kneel and/ or crouch for 80% of the shift

Nice To Haves

Previous work experience in manufacturing, operations, production or lab setting or related field
Experience in a cGMP environment
Knowledge of cGMP practices, aseptic techniques, or chemical concepts- preferred
Attention to detail
Efficient in MS Office

Responsibilities

Able to complete all Department functions in accordance with site SOPs and policies
Documentation of all activities to meet cGMP requirements
Complete preventative maintenance tasks on time
Perform timely consumption of materials
Aid in investigations/root cause analysis, and provide input on major/critical deviations
Participate in shift exchanges, 1-1’s, meetings, and site meetings
Practices and promotes safe