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Quality Control Microbiology Analyst

Ref: JN-022023-402538

Publié le 23 February 2023
Sciences de la vie

Minimum 3 months opportunity as Microbiology Quality Control Analyst for a leader in the pharmaceutical industry. 

Your Responsibilities:

  • Microbiological testing of raw materials and drug products according to incoming testing, release
  • and stability specifications.
  • Environmental monitoring of cleanrooms (microbiological and particles tests), compressed air, and
  • waters (microbiological tests, TOC, conductivity, nitrates).
  • Microbiological validation activities (writing of protocols, execution of validation, writing of reports).
  • Review of analytical raw data generated in the Microbiology Laboratory.
  • Supply management of consumables, including purchase requisitions.
  • Release of culture Media (growth promotion testing) and material used in Microbiology laboratory.
  • Identifications of microorganisms.
  • Execution and review of simple analyses such as packaging components testing, AQL, visual
  • inspection of pharmaceutical products.
  • Support to maintenance/calibration of equipment and keeps relationship with suppliers.
  • Training of other members of Quality Control or other departments.
  • General laboratory tasks (sample management, waste disposal management, cleanings).
  • Creation and update of procedures, work instructions and other QC documents.
  • Participation and presentations at team meetings .
  • Participation in projects and implementation of continuous improvement actions in the laboratory.

Your Qualifications:

  • Good knowledge of microbiology testing according to compendial harmonized methods.
  • Good knowledge of environmental and water monitoring.
  • Good knowledge of good microbiological practices and contamination control concepts.
  • Knowledge of microbiological method validation according to compendial harmonized methods.
  • Good knowledge of laboratory safety rules.
  • Good knowledge of the general organization of a quality control laboratory.
  • Good knowledge and ability to apply GDP and GMP rules.
  • General computer literacy (Windows and MS Office) and ability to use a LIMS.
  • Fluency in French and professional command of English.
  • Good collaboration and communication with QC members and other departments.
  • Able to work autonomously and collaboratively within a team.
  • Basics of the "LEAN" philosophy and 5S concept.
  • Pragmatic, structured, with good organizational skills.
  • Flexible, able to adapt to change.