Quality Assurance – Material Management Technician

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VIVEbiotech
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Description

We are looking for a Quality Assurance – Material Management Technician to fill this key position reporting directly to the Head of Quality Assurance – Material Management.

He/she will be responsible for ensuring that the necessary activities are carried out in the Company to comply with the applicable “Regulatory Requirements” and the “Quality Management System” in the Manufacturing and Material Management activities.

He/she will also provide active support in the continuous improvement of the quality system and in the implementation of new IT systems and technologies for the overall improvement of the Quality area of the Company.

We value experience in the use of computer systems and similar roles within the pharmaceutical industry with certification in GMP Part IV (GMP Guidelines specific to Advanced Therapy Drugs), Annex I Sterile Drug Manufacturing, and experience in regulated environments under FDA requirements, as well as experience in root cause analysis and risk management.

More information and contact

 We are a Contract Development and Manufacturing Organization (CDMO) with over 40 biotech companies worldwide that have placed their trust in us. We develop and manufacture lentiviral vectors as a European leader working under both EMA and FDA standards. The lentiviral vectors produced by VIVEbiotech are used to treat a range of disorders, including haematological and solid cancers, and rare diseases.

 We are looking for you to be part of our Team!

Access our website to learn more about this offer and send us your CV.

https://www.vivebiotech.com/en/work-with-us/job-vacancies/quality-assurance-technician/