Quality Control Microbiologist Lisboa

In the context of a laboratory to provide services for the Pharmaceutical Industry, we are looking for a Microbiologist with expertise in working in Quality Control Laboratory (GMP regulated).

QPLAB is a GMP certified laboratory with
-
- end services for the Pharmaceutical industry to approve and release medicinal products in the EU: Analytical services and EU Batch certification.

Responsibilities

• Perform microbiological testing of pharmaceutical products including identification of microorganisms, evaluation of results and elaboration of appropriate documentation.
• Perform growth promotion tests and approve all lab media.
• Support the validation activities of microbiological analysis, including the execution of tests, evaluation of results, elaboration of protocols and reports.
• Participate in investigations associated with out of specification or out of trend product testing results.
• Participate in laboratory management including managing laboratory stock and replenishing inventories.
• Support GMP inspection readiness in the laboratory. Improve lab quality systems; develop content, create and review SOPs and training as necessary.
• Communicate (verbally and in writing) proactively, be a team player and be a valuable contribution in order to provide the best service possible to each customer.

Qualifications

• University or Technical degree in Microbiology, Biochemistry, pharmaceutical sciences or similar.
• Experience in the Pharmaceutical Industry area (minimum 1 year).
• Proven experience in a GMP regulated Pharmaceutical Industry QC laboratory environment (mandatory).
• Proven experience in a GMP Microbiology/Environmental Monitoring Laboratory, associated with product testing.
• Demonstrated proficiency in microbiological laboratory techniques including, but not limited to Bioburden testing, specific microorganism detection and water analysis.
• Ability to work in a lab environment including wearing appropriate PPE and other safety related equipment or considerations.
• Deep understanding of compliance requirements and regulatory expectations.
• Knowledge of basic office tools and good knowledge of English (written and spoken).
• Additional preferences: experience in preservative effectiveness test or rapid microbiological test methods; knowledge of method validation according to ICH guidelines.

Seniorities

• Entry level

Employment type

• Full-time

Job function

• Research, Analyst, and Information Technology

Industries

• Pharmaceutical Manufacturing

We are seeking to maintain compliance and
- quality standards in all lab activities aligned with GMP requirements.