Work ScheduleFirst Shift (Days)Environmental ConditionsAble 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 Description2nd Shift: Rotating 4 10's - 10%Location/Division Specific InformationSt. 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 systemsIdentify 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:Education:HS Diploma/ GED required, bachelor's degree preferredExperience:2 years relevant work experience is required Experience in cGMP environment preferredKnowledge, Skills, AbilitiesKnowledgeKnowledge of cGMP practices, aseptic techniques, or chemical concepts- preferredSubject Matter Expert on downstream processing stepsSkillsStrong math skillsCritical thinking and problem-solving capabilitiesDetail OrientedResults DrivenEfficient in MS OfficeQualified to train other employees- preferredQualified to train (preferred) and guide employees.AbilitiesCritical evaluation of processes, including foresight and thinking ahead.Able to read, write, and communicate in EnglishAble to understand and carry out instructionsReliableEffectively multi-taskAble to work in an environment of changeAble to work independently and as part of a teamAble to recognize problems developing, not just occurringSeeks and welcomes feedback and responds to coaching.Physical Requirements / Work EnvironmentBe 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 glovesAbility to lift minimum of 25 lbs independentlyAbility to stand for 80% of shiftThermo Fisher Scientific Inc. is an equal opportunity employer and offers accessibility services for job seekers requiring accommodations in the application process. If you require an accommodation or assistance due to a disability, please contact us at 1-855-471-2255. We value diversity and are committed to crafting an inclusive and collaborative environment where all perspectives are valued. Join us today and start your story at Thermo Fisher Scientific!