Head (m/f/d) Manufacturing Unit BioII/III

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.

The Position

A healthier future. It’s what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come.

Creating a world where we all have more time with the people we love. That’s what makes us Roche.

Purpose

As a member of the Site Leadership Team, the Head (m/f/d) of Manufacturing Unit BioII/III is accountable for overseeing the entire process of turning raw material into drug substance (make-assess-release) of established commercial products. The role focuses on ensuring operational excellence, continuous improvement, and the resilience of the supply chain, while maintaining the highest levels of safety and quality compliance.

This area of manufacturing is characterized by: mono products, low number of deviations, optimized product costs, routine work, high degree of automation and little production process changes.

Key Responsibilities

Strategic Leadership & Manufacturing Execution:

• As Head of Manufacturing, you will have full accountability for the entire drug substance production process in the EPO & CERA space, ensuring delivery, quality, and cost-effectiveness. You will build and maintain a robust supply chain, collaborating with other departments to ensure material availability. Additionally, you will provide strategic consulting to the site head, formulate vision, and lead key projects to develop long-term business strategies.

Operational Excellence & Continuous Improvement:

• Drive continuous improvement, implement Lean practices, and optimize manufacturing processes for efficiency and robustness.

Compliance & Quality Assurance:

• Ensure adherence to cGMP and quality standards, manage deviations, and maintain inspection readiness.

Team Leadership & Development:

• Lead and develop a high-performing, multi-disciplinary team, fostering innovation and growth

Cross-Functional Collaboration & Network Integration:

• Partner with stakeholders and the global network to align on operational goals and initiatives.

Safety, Cost, and Financial Performance:

• Ensure safety, manage budget, and optimize cost per gram as a key productivity metric

• Responsibility for a 70 million capex invest in order to refurbish the aged facility to higher standards

Overall Accountability:

• Take full ownership of drug substance production, including quality, delivery, and cost, managing a large team and budget.The role is has a FTE responsibility of roughly 140 FTE in two different manufacturing buildings and a budget accountability of around 20 millions

Qualifications

Education:

• BS/BA degree in life sciences, physical sciences, engineering, or an equivalent combination of education and experience

• Master and/ or PhD with 10-15years leadership experience

• Post-graduate education or management training (e.g., MBA) is highly desirable

Experience:

• Experience in biotechnology within the diagnostics or pharmaceutical sectors is essential

• Extensive experience in biopharmaceutical manufacturing, including cross-functional leadership and proven success in end-to-end pharmaceutical business execution

• Deep understanding of cGMP, quality systems, and regulatory standards

• Expertise in LEAN manufacturing and process optimization under stringent regulatory conditions

Skills:

• Strong leadership in the Visionary, Architect, Coach, Catalyst (VACC) model, with the ability to remove barriers and foster collaboration across Manufacturing Units

• Demonstrated capability to apply Lean Manufacturing principles, enhance operational efficiency, and drive continuous improvement

• Proven track record of building high-performing, cross-functional teams in complex, regulated environments

• Change management expertise with the ability to create a bold shared vision and lead teams through periods of uncertainty

• Strong communication skills, including experience presenting to regulatory authorities and managing inspections

• We require proficiency in both English and German. Candidates with an intermediate level of German are encouraged to apply, as we value commitment to language improvement. Roche supports continuous learning and offers resources to assist employees in enhancing their language skills.

Candidate documents

PleasesendusacurrentandmeaningfulCV.Otherdocuments,e.g.acoverletter,arewelcometobeaddedoptionally.Pleasenotebeforesendingyourapplicationthatnofurtherdocumentscanbeaddedafterwards.

Your contact to us! With people. For people.

Do you need further support?

Please have a look at our FAQs, you will find them via https://careers.roche.com/global/en/faq.

Who we are

A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.

Let’s build a healthier future, together.