QC Supervisor, CAR-T Europe

At Johnson & Johnson,we believe health is everything.

Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.

Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.

Learn more at https://www.jnj.com/.

The Janssen Supply Chain Group, a member of the Johnson & Johnson family of companies, is recruiting a QC Supervisor for the CAR-T hub in Europe.

The position will be based in Beerse Belgium.

CAR-T (chimeric antigen receptor T-cell therapy) is an innovative approach to eliminate cancer cells, which work by harnessing the power of a patient's own immune system.

They are created from the patients' own T cells and are engineered to eliminate cancer cells expressing a specific antigen.

To support the CAR-T program in EMEA, Janssen is building two CAR-T manufacturing centers in the Ghent area (Belgium).

The QC laboratories will be operated from the existing Janssen Beerse site.

The QC Supervisor Biotech oversees day-to-day planning and Quality Control activities for the Biotech Release laboratory, ensuring GMP compliance, accuracy and timeliness of specified testing processes and managing a team of QC analysts.

The QC Supervisor Biotech carries out duties in compliance with all local, state and federal regulations and guidelines (including EMA, FDA, ...) as well as all company and site policies and procedures.

This position is responsible for carrying out supervisory responsibilities in accordance with the organization's policies and applicable laws.

Responsibilities include interviewing, hiring, performance review, rewarding and disciplining employees, addressing complaints, resolving conflict and supporting internal and external audits.

Quality Leadership:


* Lead the QC Biotech team (Flow Cytometry Lab, Molecular Assay qPCR Lab, ELISA Lab) by supporting, coaching and developing team members in reaching quality, business and personal objectives


* Establish and maintain effective working relationships with business and quality partners to ensure alignment of objectives and deliverables


* Proactively and continuously challenge the organizational performance and develop and implement improvements in organizational performance

Operational Quality performance:


* Manages a team of analysts within the QC department based on assigned work, direction, coaching and developing capabilities.


* Set testing priorities and manage work assignments


* Maintain individual training completion in a compliant state


* Evaluate performance and provides opportunities for growth.


* Communicate department objectives and metrics


* Implement methods and procedures for testing, evaluation and inspection


* ...