Sr. Formulation Technician - 2nd Shift

Work Schedule First Shift (Days) Environmental Conditions 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, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.) Job Description 2nd Shift: Rotating 4 10's - 10% Location/Division Specific Information St. Louis, MO/ Drug Substance Division (Biologics) Are you ready to take your career to the next level? Thermo Fisher Scientific Inc. is seeking an individual with outstanding work behaviors to join our team as a Downstream Processing Technician III in St. Louis. This is a manufacturing role where you will have the opportunity to contribute to the production of world-class products that make a difference in people's lives. As a Downstream Processing Technician III, you will play a meaningful role in our ambitious mission to enable our customers to make the world healthier, cleaner, and safer. You will work closely with a team of proven professionals to compete in a fast-paced environment, ensuring flawless execution of downstream manufacturing processes. Your responsibilities will include: A day in the Life: Execution of manufacturing batch records, work instructions and/or SOPs, with minimal instruction on a day-to-day basis and a focus on proactive ‘right the first time’ executions. Assist with batch record reconciliation. Able to complete 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. Daily record review, tasks, and databases. Complete preventative maintenance and work notifications tasks on time. Perform equipment testing and routine trouble-shooting. Oversee and perform timely consumption of materials and completion of quality documentation in appropriate systems Identify deviations, aid in investigations/root cause analysis, and provide input on major/critical deviations. Complete validation protocols with minimal supervision or direction. Schedule activities and coordinate the shift huddle in absence of the supervisor. Act as liaison with other groups within the manufacturing organization and a Subject Matter Expert on a variety of downstream processing steps techniques. Participate in shift exchanges, 1-1’s, meetings, attend meetings as necessary to facilitate area needs based on changes, etc. (lean activities). Practices and promotes safe work habits and adheres to safety procedures and guidelines. Provides feedback on document revisions and/or document management including batch production records and manufacturing procedures. Keys to Success:

HS Diploma/ GED required, bachelor's degree preferred Experience: 2 years relevant work experience is required   Experience in cGMP environment preferred Knowledge, Skills, Abilities Knowledge Knowledge of cGMP practices, aseptic techniques, or chemical concepts- preferred Subject Matter Expert on downstream processing steps Skills Strong math skills Critical thinking and problem-solving capabilities Detail Oriented Results Driven Efficient in MS Office Qualified to train other employees- preferred Qualified to train (preferred) and guide employees. Abilities Critical evaluation of processes, including foresight and thinking ahead. 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 Able to recognize problems developing, not just occurring Seeks and welcomes feedback and responds to coaching. Physical Requirements / Work Environment Be willing to wear a full gowning suit which includes: bodysuit, gloves, hair & beard nets, face covers, and safety glasses. (These