QC Manager Micro, CAR-T Europe

Job title:

QC Manager Micro, CAR-T Europe

Company:

Johnson & Johnson

Job description

· Flexible work practices, award-winning benefits· This position will be based in Beerse, Belgium.Change lives for the better.At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions 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 atTHE OPPORTUNITYHow you can help.The Janssen Supply Chain Group, a member of the Johnson & Johnson family of companies, is recruiting a QC Manager Micro for the CAR-T hub in Europe. The position will be based in Beerse, Belgium.At the Janssen Pharmaceutical Companies of Johnson & Johnson, we are working to create a world without disease. Transforming lives by finding new and better ways to prevent, intercept, treat and cure disease inspires us. We bring together the best minds and pursue the most promising science. We are Janssen. We collaborate with the world for the health of everyone in it. Learn more at and follow us @JanssenGlobal. Janssen Biotech, Inc. is part of the Janssen Pharmaceutical Companies.Janssen Biotech, Inc., one of the Janssen Pharmaceutical Companies of Johnson & Johnson, and Legend Biotech USA Inc., have entered a global, strategic collaboration to develop, manufacture, and commercialize a chimeric antigen receptor (CAR) T-cell therapy. This innovative strategic partnership is designed to combine the strengths and expertise of two companies to advance the promise of an immunotherapy CAR T platform and investigational treatment.The QC Manager Micro, CAR-T will oversee and lead the Micro labs in Early/Late – day and weekend shift regime. The Micro release lab is focusing on release & stability testing and supporting tests such as Environmental Monitoring testing and growth promoting testing.What you’ll do.Key activities include, but are not limited to:

• Responsible for the day-to-day oversight on all the micro related activities.
• Provide QC input for site continuous improvement and remediation efforts. Schedule and manage QC tasks associated with these efforts.
• Support and lead quality control continuous improvement projects.
• Act as liaison for the quality control team in support of site improvement projects and strategies.
• Collaborate with functional departments to resolve issues.
• Manage cross-functional projects with many stakeholders.
• Oversee timely completion of laboratory investigation of OOS/ invalid assays, CAPAs and change controls.
• Mentor, train, and supervise quality control staff.
• Evaluate performance and provides opportunities for growth.
• Require minimal direction to complete tasks, know how to get resources and information from established internal contacts; consult with supervisor for decisions outside of established processes.
• Perform tasks in a manner consistent with the safety policies, quality systems and cGMP requirements.
• Other duties will be assigned, as necessary.

QualificationsIT’S ALL ABOUT YOUTo be successful, you demonstrate the ability to communicate effectively at all levels within a virtual matrix environment. Further requirements include:· A minimum of a Master Degree in Science or equivalent experience is required.· Experience leading, coaching, or supervising direct or indirect personnel or teams.· Strong communication and interpersonal skills, a high level of organizational ability, attention to detail, and ability to work effectively in a collaborative environment globally (US and EU) is required.· Proficient knowledge of Micro technologies used in a Quality Control laboratory.· Experience working with Quality Systems.· Detailed knowledge and understanding of current Good Manufacturing Practices (cGMP) related to the QC laboratory and ability to identify/remediate gaps in processes or systems is required.· Good written and verbal communication skills.· Knowledge of Good Tissue Practice and experience with cell-based manufacturing is preferred.· Experience with LIMs and SAP or equivalent systems is preferred.· Lean Six Sigma Certification is preferred.Being part of Johnson & Johnson can change everything, including YOU
For more than 130 years, diversity, equity & inclusion (DEI) have been part of our cultural fabric at Johnson & Johnson and woven into how we do business every day. Our commitment to respect the dignity and diversity of all is embedded in our Credo.We know that the success of our business depends on having the best talent in a workforce that reflects the diverse markets we serve around the world and an inclusive culture that values different perspectives and life experiences.That is why we are working to create an inclusive environment where diverse backgrounds, perspectives and experiences are valued and each and every one of our people feels that they belong and can reach their potential. No matter who they are.Diversity, Equity & Inclusion at Johnson & Johnson means “You Belong”!Closing date: Thursday, 15 th of August 2024.

Expected salary

Location

Beerse, Anvers

Job date

Sat, 03 Aug 2024 00:33:17 GMT

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