Sr. Formulation Technician

Thermo Fisher Scientific•St. Louis, MO

3d•Onsite

About The Position

Thermo Fisher Scientific Inc. is seeking a highly skilled and motivated Downstream Processing Technician III to join their world-class team in St. Louis. This role involves playing a vital part in the flawless execution of manufacturing batch records, work instructions, and SOPs. The technician will assist in maintaining the suite, supplies, equipment, logbooks, and data to strict cGMP standards, contributing to the success of manufacturing operations. The position emphasizes a proactive 'right the first time' approach and requires critical evaluation of processes, foresight, and prioritization based on production schedules.

Requirements

High school diploma or equivalent with +2 years of experience OR Bachelor's Degree
Able to lift 40 lbs. without assistance
Adherence to all Good Manufacturing Practices (GMP) Safety Standards
Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed
No contact lens allowed; prescriptive glasses will be provided
Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)
Standing for full shift
Will work with hazardous/toxic materials
Knowledge of cGMP practices, aseptic techniques, or chemical concepts
Critical thinking and problem solving
Strong math skills
Detail oriented
Results Driven
MS Office
Be willing to wear a full gowning suit which includes: bodysuit, gloves, hair & beard nets, face covers, and safety glasses.
Ability 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 for 80% of shift
Able to read, write, and communicate in English
Able to understand and carry out instructions
Reliable
Effectively multi-task
Able to work in an environment of change
Able to work independently and as part of a team

Nice To Haves

Experience in a manufacturing, operations, production, lab setting or related field
Experience in a cGMP environment
Subject Matter Expert on processing steps
Qualified to train other employees

Responsibilities

Execution of manufacturing batch records, work instructions and/or SOPs, with focus on proactive ‘right the first time’ executions.
Assist with batch record reconciliation.
Assist in all Department functions, such as maintaining suite, supplies, equipment, logbooks and data in accordance with site SOPs and policies.
Documentation of all activities to meet cGMP requirements.
Complete document reviews and revisions.
Daily record review, tasks, and databases.
Actively provide feedback.
Participate/Lead in shift exchanges, 1-1’s, meetings, attend meetings as needed to facilitate area needs based on changes, etc. (lean activities).
Support a quality investigation by answering questions, providing feedback and making suggestions for improvement.
Practices and promotes safe work habits and adheres to safety procedures and guidelines.
Critical evaluation of processes, including foresight and thinking ahead.
Ensure tasks are performed with a method of prioritization - interpret production schedules and complete tasks accordingly.