Supervisor, Buffers & Media

at  Thermo Fisher Scientific

St. Louis, MO 63134, USA -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate04 Dec, 2024Not Specified04 Sep, 20242 year(s) or aboveDisabilities,Pharmaceutical Industry,Cgmp Practices,Analytical Skills,Communication SkillsNoNo
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Description:

REQUIREMENTS:

  • Equivalent experience accepted; Bachelor’s degree in science or engineering preferred
  • 2+ years of supervisory experience in the pharmaceutical industry preferred
  • 3+ years of proven experience in a related field or industry required
  • Knowledge of cGMP practices and deviation investigations preferred
  • Strong mechanical and analytical skills
  • Proficiency in MS Office and strong math skills
  • Meticulous with strong prioritization and communication skills
  • Able to work independently and as part of a team
  • Strong problem-solving and decision-making abilities
    Thermo Fisher Scientific is an equal opportunity employer and provides reasonable accommodations for applicants with disabilities. We value diversity and inclusion in our workforce, and we are committed to creating a supportive and inclusive environment for all employees.
    Apply today to be part of our exceptional team! Visit http://jobs.thermofisher.co

Responsibilities:

  • Maintain a safe and clean work environment, ensuring compliance with established policies and procedures
  • Follow manufacturing batch records and work instructions with a focus on achieving flawless execution.
  • Complete department functions such as equipment maintenance, documentation, and data management
  • Act as an On-The-Job Trainer for various job functions
  • Document all activities to meet cGMP requirements and actively provide feedback
  • Evaluate processes critically and identify areas for improvement
  • Perform equipment testing, troubleshooting, and routine maintenance
  • Schedule and assign personnel, prioritize tasks, and supervise progress
  • Complete production plan, ensuring timely consumption of materials and quality documentation
  • Identify deviations, aid in investigations, and provide input on major deviations
  • Participate in cross-functional teams and act as a Subject Matter Expert


REQUIREMENT SUMMARY

Min:2.0Max:3.0 year(s)

Pharmaceuticals

Production / Maintenance / Quality

Clinical Pharmacy

Graduate

Science or engineering preferred

Proficient

1

St. Louis, MO 63134, USA