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Sr Formulation Technician - DSP

Sr Formulation Technician - DSP

Thermo Fisher ScientificSt. Louis, Missouri, United States of America
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SrDownstream Processing Technician .Location / Division Specific Information.Louis, MO / Drug Substance Division (Biologics). Are you ready to take your career in manufacturing to the next level? Therm...serp_jobs.internal_linking.show_moreserp_jobs.last_updated.last_updated_variable_days
Direct Support Professional (DSP)

Direct Support Professional (DSP)

St. Louis ArcSaint Louis, Missouri, United States
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We empower people to live their best life.That is our mission—not only to those we serve, but to those we employ.This mutually shared sense of purpose drives our decisions and actions.Come as you a...serp_jobs.internal_linking.show_moreserp_jobs.last_updated.last_updated_variable_days
Sr Formulation Technician - DSP

Sr Formulation Technician - DSP

Thermo Fisher ScientificSt. Louis, Missouri, United States of America
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  • serp_jobs.job_card.full_time
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Job Title : SrDownstream Processing Technician

Dayshift : 6am – 6 : 30pm

Nightshift : 6pm – 6 : 30am

Location / Division Specific Information

St. Louis, MO / Drug Substance Division (Biologics)

Are you ready to take your career in manufacturing to the next level? Thermo Fisher Scientific Inc. is currentlyseekinga highly skilled and motivated Downstream Processing Technician III to join our world-class team in St. Louis. As a leading company in the scientific research industry, we are dedicated to enabling our customers to make the world healthier, cleaner, and safer.

In this role, you will have the opportunity to work with a team of exceptional professionals and play a vital role in the flawless execution of manufacturing batch records, work instructions, and SOPs. Your keen attention to detail and proactive approach will ensure that all tasks are completed right the first time.Additionally, you will assist in maintaining the suite, supplies, equipment, logbooks, and data to strict cGMP standards, contributing to the success of our manufacturing operations.

A day in the Life :

Execution of manufacturing batch records, workinstructionsand / or SOPs, withfocuson proactive ‘right the first time’ executions.Assistwith batch record reconciliation.

Assistin all Department functions, such asmaintainingsuite, supplies, equipment,logbooksand datain accordance withsite SOPs and policies.

Documentation of all activities to meetcGMPrequirements. 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 tofacilitatearea needs based on changes, etc. (lean activities).

Support a quality investigation by answering questions, providingfeedbackand 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 -interpretproduction schedules andcompletetasks accordingly.

Keys to Success : Education :

Required : High school diploma orequivalent

Preferred : Associates Degreew / +2 years of relevant years of experience orBachelor'sdegree

Experience :

Required : Minimum of 2years experienceinamanufacturing, operations, production, lab setting or related field

Preferred : Experience in a cGMP environment

Knowledge, Skills, Abilities

Knowledge

Knowledge of cGMP practices, aseptic techniques, or chemical concepts- preferred

Subject Matter Expert on processing steps- preferred

Skills

Critical thinking and problem solving

Strong math skills

Detail oriented

Results Driven

MS Office

Qualified to train other employees- preferred

Abilities

Able todemonstratepractical knowledge with successful outcomes

Able to recognize problems developing, not just occurring

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

Physical Requirements / Work Environment

Be willing to wear a full gowning suit whichincludes : bodysuit, gloves, hair & beard nets, face covers, and safety glasses. (These items are prohibited : makeup, jewelry, nail polish, cologne / perfume, scentedlotionsor 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 25lbsindependently

Ability to stand for 80% of shift

Join Thermo Fisher Scientific and be part of our ambitious team that strives for excellence in everything we do. We are an equal opportunity employer, committed to fostering an inclusive and diverse workforce. We value the unique perspectives and contributions of all individuals and actively encourage candidates from all backgrounds to apply.

To apply, please visit our career website at

Thermo Fisher Scientific Inc. is an EEO / Affirmative Action Employer andprovidesequal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other legally protected status.

If yourequireanyaccommodationsduring the application process due to a disability, please contact us at 1-855-471-2255

  • . We are here to support you and ensure that you have an equal opportunity to succeed.

This telephone line is reserved solely for applicants with disabilities requiring accessibilityassistanceoraccommodations. Messages left for other purposes will not receive a response.