22 Mar, 2024

Process Engineer III

  • Thermo Fisher Scientific
  • St. Louis, MO, USA
Process Engineer Biochemicals / Pharmaceuticals

Job Description

Job Description

How will you make an impact?

We are searching for a Process Engineer with experience in biologics processing. This member of our team provides technological input in the transfer, development, and continuous of a manufacturing process and is the technical owner while running customer programs in clinical manufacturing. They also contribute more broadly to defining and shaping Thermo Fisher Scientific’s own technology programs.

This role will collaborate with customers, supervisors and technicians in the Operations department, Quality Assurance, fellow Engineers, line management, and scientists in Process Development. These activities are often carried out in projects, and involve teamwork with experts across functional groups to ensure project success.

This position's work schedule requires the applicant to work overnight in support of a 24/7 clinical and commercial operations.

What will you do?

  • Tackle technical challenges on the manufacturing floor as needed.
  • Provide scientific expertise for GMP deviations.
  • Create detailed GMP documentation including Process Flow Diagrams, Standard Operation Procedures, and Job Aids.
  • Draft and own Manufacturing Batch Records ensuring the process is technically accurate and Designed for Manufacturing
  • Work with process development to develop standardized methodologies for conducting unit operations at the manufacturing scale including cell culture, harvest, chromatography, ultrafiltration, and depth filtration.
  • Actively drive engineering initiatives to improve practices and procedures
  • Help devise and Implement Corrective and Preventative Actions.
  • Provide technical feedback on documents created by other departments, such as Tech Transfer Protocols and SOPs.
  • Contributes to Internal and Customer meetings based upon sound evidence.
  • Support our MSAT team with additional tasks to improve the site, ensure patient safety, and deliver for our customers.
  • Support changes to equipment and processes.
  • Support projects with support from supervision as needed.

How will you get here?

Education

  • Bachelor’s degree required in a scientific field, preferably an engineering field Experience
  • 4+ years of experience in GMP regulated Biologics / Pharma Industry, or equivalent experience.
  • Follow Environmental Health and Safety policies and procedures and ensure a safe and healthy workplace environment.
  • Ability to self-motivate, prioritize work and time.
  • Demonstrates a foundation in general scientific practices, principles, and concepts.
  • Writes and communicates effectively.
  • Ability to work both independently and as part of a team.
  • Knowledge of current Good Manufacturing Practices and US/EU regulations.
  • Knowledge of statistical methods used for Pharmaceutical Process Analysis
  • Proficient in Microsoft Word and Excel.
  • Ability to stand for long periods of time and gown into manufacturing areas.

Relocation Benefits

This position does not offer relocation benefits.

Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory at Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.

Apply today! http://jobs.thermofisher.com

Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

Accessibility/Disability Access

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