Quality Control Assistant (M/F)

Edmond Pharma S.R.L.; Lisboa; Presencial; EUR 25 000 - 40 000; Tempo integral

Resumo da oferta

Edmond Pharma S.R.L. is seeking a QC Analyst to join the laboratory team in the QC department, reporting to the QC Laboratory Manager. The role involves executing routine analyses and supporting in-process product control under cGMP guidelines.

Requirements include a degree in Microbiology/Biology/Biotechnology or related field, 1–2 years in pharma, GMP knowledge, and good English. Flexibility for two shifts and strong teamwork are expected. Based in Lisbon, on-site position.

Qualificações

• Minimum 1-2 years of work experience in similar roles in pharmaceutical industry.
• Knowledge of Good Manufacturing Practices (GMP).
• English language knowledge is required.

Responsabilidades

• Perform physiochemical and microbiological analysis for in-process product control per cGMP procedures.
• Sample raw materials and packaging materials per established procedures.
• Perform routine environmental monitoring of manufacturing facilities and support areas.
• Sample and analyze water for injectables (WFI) per procedures.
• Support QC investigations on deviations or OOS events.
• Assist QC team in preparing protocols for new assays/methods.
• Ensure QC facilities are clean and organized and laboratories are monitored.
• Execute routine analyses to support the manufacture of the first FDA-approved oral microbiome product.

Conhecimentos

Strong organizational skills

Good team spirit

Good knowledge of English

Shift flexibility

Formação académica

Degree in Microbiology, Biology, Biotechnology or Engineering Sciences (Chemical, Biochemical,Biologicalor similar) or certification in QC Microbiology techniques

Descrição da oferta de emprego

This person will integrate the laboratory team of the QC department and will report directly to the QC Laboratory Manager. This person willbe responsible forthe execution of routine analysis.

We´re looking for people who have:

• Degree in Microbiology, Biology, Biotechnology or Engineering Sciences (Chemical, Biochemical,Biologicalor similar) or certification in vocational course in QC Microbiology techniques;
• Minimum 1-2 years of work experience in similar roles in pharmaceutical industry;
• Knowledge of Good Manufacturing Practices;
• Strong organizational skills and motivation to work in an innovative industry;
• F lexibilityto work in 2 shifts (8h-15h and 15h-01ham);
• Good team spirit;
• Good knowledge of English.

Technical/Functional Responsibilities:

• Perform the physiochemical and microbiological analysis specificallyrequiredfor in process product control, ensuring compliance with established procedures and current Good Manufacturing Practice (cGMP);
• Perform the sampling of raw materials and packaging materials, ensuring compliance with established procedures and current Good Manufacturing Practice (cGMP);
• Perform routine environmental monitoring of the manufacturing facilities and support areas according to the procedures in place;
• Perform the sampling and analysis of water for injectables (WFI), according to the procedures in place;
• Support QC investigation on deviations or OOS events;
• Support QC team in the preparation of protocols for the implementation of newassays/methods;
• Guarantee Quality Control’sfacilitiescontinuous monitoring, ensuring the laboratories are clean and organized.
• This person will execute routine analyses to support the manufacture of the first FDA-approved oral microbiome product