Quality Control Assistant (M/F)

Recipharm; Lisboa; Presencial; EUR 17 000 - 21 000; Tempo integral

Resumo da oferta

Recipharm in Lisbon is seeking a Quality Control Assistant to join the QC laboratory team and report to the QC Laboratory Manager. You will execute routine analyses to support the manufacturing process.

Responsibilities include performing physiochemical and microbiological analyses under cGMP, sampling materials, environmental monitoring, and assisting in method development. The role includes two shifts and requires English proficiency.

Qualificações

• Degree in Microbiology, Biology, Biotechnology or Engineering Sciences (Chemical, Biochemical, Biological or 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;
• Flexibility to work in 2 shifts (8h-15h and 15h-01ham);
• Good team spirit;
• Good knowledge of English.

Responsabilidades

• Perform the physiochemical and microbiological analysis specifically required for 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 new assays/methods;
• Guarantee Quality Control’s facilities continuous 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.

Conhecimentos

Strong organizational skills

Flexibility to work 2 shifts

Good team spirit

Good knowledge of English

Knowledge of GMP

Experience in pharma industry

Formação académica

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

Descrição da oferta de emprego

Quality Control Assistant ( M/F)

Lisbon

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

We´re looking for people who have

• Degree in Microbiology, Biology, Biotechnology or Engineering Sciences (Chemical, Biochemical, Biological or 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 lexibility to 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 specifically required for 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 new assays/methods;
• Guarantee Quality Control’s facilities continuous 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.

Recipharm is a leading Contract Development and Manufacturing Organisation (CDMO) employing over 4,500 employees worldwide. Recipharm provides manufacturing services of pharmaceuticals in various dosage forms, including, sterile fill & finish, oral solid dosage and biologics; clinical trial material development and manufacturing services; and, pharmaceutical product development. Its biologics segment, ReciBioPharm, works with customers to develop and commercialise advanced therapy medicinal products (ATMPs): pre-clinical to clinical and commercial development and manufacture for new biological modalities, encompassing technologies based on live viruses and viral vectors, live-microbial biopharmaceutical products, nucleic acid-based mRNA and plasmid DNA production.

Recipharm manufactures several hundred different products to customers ranging from big pharma to smaller research and development companies. It operates development and manufacturing facilities in France, Germany, India, Italy, Portugal, Spain, Sweden and the US and is headquartered in Stockholm, Sweden.