Team Leader Quality Control Laboratory

We are a Contract Development and Manufacturing Organization (CDMO) with over 20 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!

We are looking for a Team Leader Quality Control Laboratory to fill a key position reporting directly to the Quality Control Manager. You will be responsible for managing the daily operations required for the analytical characterization of the final and intermediate products generated during the manufacturing process.

Your main mission will be to ensure the proper release of analytical test results while maintaining the highest quality standards. He/she will review the documentation associated with each assay (CQMs and records) on time, ensuring the correct traceability of samples and guaranteeing full data integrity.

The Quality Control Team leader will ensure the correct coordination and integration of his team with the other areas of the department such as Environmental Control, Analytical Development and Laboratory Management Support. As part of his/her mission, he/she will report on activities and incidents to the QC and Analytical Development Manager.

The QA Team Leader will work closely with the Environmental Control, Analytical Development and Document Management areas to ensure the smooth running of the daily operations of the department. He/she will coordinate analytical assay execution activities with the USP and DSP Production and Development departments. Coordinate quality system management activities (Deviations, CAPAS and change controls) with the Quality Assurance area. You will maintain contacts with external suppliers and participate in the evaluation of DEMO equipment for the incorporation of new technologies in the department.

We value having more than 3 years of industry experience in the life sciences or pharmaceutical area. Experience working with GMP or GLP (E) standards. Demonstrable experience in leadership and team management: training, mentoring and supervision of laboratory personnel.

Thank you!