Supervisor, Quality Control Microbiology

In this position, you will lead, coach, and develop a team while fostering a collaborative and supportive team culture. Oversee routine laboratory operations and ensure efficient planning and execution of activities. Coordinate cross-functional projects across QC and QA and support continuous improvement initiatives. Manage deviations, perform root cause analyses, and implement effective corrective and preventive actions (CAPAs). Support qualification activities and oversee equipment lifecycle management, including maintenance and decommissioning. Contribute to the development and optimization of laboratory systems and GMP documentation. Prepare and review GMP documentation, including trend reports and other quality-related records. Ensure compliance with cGMP, internal procedures, and external regulatory requirements (USP, EP, FDA, EU guidelines). Represent the team during regulatory inspections and customer audits and ensure strong inspection readiness. Deliver training and support knowledge sharing within the team. Contribute to budget planning and resource management.

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. As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.

• Degree in Biology, Microbiology, Food Technology, or a related scientific field (PhD is an advantage)

• Several years of experience in microbiology quality control and/or sterile (aseptic) environments

• Experience leading teams and/or coordinating projects in a regulated environment

• Familiarity with EU and FDA regulations, as well as cGMP and cGLP requirements

• Strong communication and collaboration skills, with the ability to work across functions

• A structured and solution-oriented approach to problem-solving

• Fluency in German and English (written and spoken)

• Good knowledge of MS Office tools