QC Technician I (Microbiology)
When you join us at Thermo Fisher Scientific, you’ll be part of a smart, driven team that shares your passion for exploration and discovery. With revenues of $22 billion and the largest investment in R&D in the industry, we give our people the resources and opportunities to make significant contributions to the world.
Location/Division Specific Information
St. Louis, MO
How will you make an impact?
Provide support in microbiology by following standard practices. Perform sample management (receipt/disposal) of in-process samples, raw materials, buffers, media, etc. Perform inventory and stocking of QC microbiology supplies. Support internal development and/or manufacturing operations. Support the microbiology lab to produce efficient results.
What will you do?
· Perform receipt, storage and disposal of samples submitted to the microbiology lab.
· Perform raw material disposal following appropriate safety and quality procedures.
· Recognize and report events clearly and accurately.
· Perform inventory and expiration checks of materials in the laboratory. Dispose or order materials as needed.
· Perform growth promotion testing
· Perform support for bioburden and endotoxin testing.
· Contribute to writing of SOPs if needed.
· Perform daily lab cleaning, preventative maintenance of equipment, ordering of supplies, and autoclaving of equipment.
· Perform all duties in strict compliance with Standard Operating Procedures, Good Manufacturing
· Practices, Good Laboratory Practices, and Safety guidelines.
· Maintain the necessary compliance status required by company and facility standards.
- Perform testing supply support for EM group with transporting materials to production
- Support environmental monitoring testing when needed, specifically assist with non-routine
How will you get here?
Education
Associates' degree in Science; preferably Microbiology or Biology
Experience
· 0 to 2 years of previous lab experience
· Equivalent experience working in a cGMP environment
Knowledge, Skills, Abilities
· Knowledge of GMP regulations in cGMP manufacturing environment.
· Excellent problem solving and critical thinking skills
· Excellent organization and planning skills.
· Strong attention to detail and ability to adhere to standard procedures.
· Ability to function in a rapidly changing environment
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