Sr Buffers & Media Technician

at  Thermo Fisher Scientific

DISCOVER IMPACTFUL WORK:

Thermo Fisher Scientific Inc. is seeking a highly skilled and motivated Sr Manufacturing Technician to join our world-class team in St. Louis. As a Manufacturing Technician, you will play a critical role in the production of Commercial and Clinical Biologics. This is a unique opportunity to contribute to the manufacturing process and make a significant impact on the development of life-saving products.

REQUIREMENTS:

• HS Diploma/ GED required, 0-4 years’ experience required based on education. Alternatively, an Associates Degree with +2 years of relevant experience or a Bachelor’s degree.
• Experience in a manufacturing and/or GMP environment preferred.
• Knowledge of cGMP practices, aseptic techniques, or chemical concepts preferred.
• Strong critical thinking, problem-solving, and math skills.
• Focused on attention to detail and achieving desired outcomes.
• Proficiency in MS Office.
• Ability to effectively multi-task and work independently or as part of a team.
  Thermo Fisher Scientific Inc. offers a competitive remuneration package, annual incentive plan bonus, healthcare benefits, and an exhilarating company culture. Join our team and be part of an organization dedicated to making the world healthier, cleaner, and safer.
  Thermo Fisher Scientific Inc. is an equal opportunity employer and values diversity. We are committed to providing reasonable accommodations to individuals with disabilities throughout the job application process. If you require any accommodations, please contact us at 1-855-471-2255*.

Apply today at http://jobs.thermofisher.com and start your story with Thermo Fisher Scientific Inc.

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• Follow Current Good Manufacturing Practices (cGMPs) to ensure flawless execution of Buffer and Media manufacturing tasks.
• Carry out buffer and media weighing, formulation, and in-line conditioning (ILC) skid work.
• Assist with batch record reconciliation and maintain suite, supplies, equipment, logbooks, and data in accordance with site SOPs and policies.
• Complete documentation to meet cGMP requirements, including document reviews and revisions.
• Participate in meetings and lean activities to facilitate area needs based on changes.
• Support quality investigations by providing feedback and suggestions for improvement.
• Promote and adhere to safety procedures and guidelines.