Program Manager
This role is primarily based on site. Working together in person supports close, real‑time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards. We offer flexibility to work remotely for no more than 20% of your time. Requests are considered on a case‑by‑case basis, in line with business needs.
The Program Manager is responsible for Managing projects which requires a unique set of skills that are consolidated into the role of Program Manager (PM). This crucial position sits at the center of a triangle made up between Lonza, our Customers and their Patients. You will therefore be responsible for ensuring relationships are built and that the project/program is delivered according to the expected quality, timelines and cost.
An agile career and dynamic working culture.
An inclusive and ethical workplace.
Compensation programs that recognize high performance.
Medical, dental and vision insurance.
And much more.
B e the interface between the Customer and Lonza to ensure execution and delivery according to Lonza and the Customer’s expectations
Understand the Customer’s needs and represent their interests by acting as their advocate on-site
Fully accountable for all operational aspects in leading and motivating cross-functional project teams to deliver on all scope objectives with the highest level of quality
Ensure adherence to Global Program and Project Center of Excellence (PPM CoE) Standards, including maintenance of data integrity excellence in Planview
P assionate about customer focus with a true “Customer Comes First” mindset and constantly seeks opportunities to improve performance through partnership and collaboration
A ble to translate the strategic vision for the project into actionable objectives and plans that are ambitious but achievable
E qually comfortable functioning in a scientific or technical environment as well as in a purely business-related setting
Bachelor's Degree is required, preferred to have degree in related Life Sciences or STEM discipline. PMP preferred.
Highly preferred to have 5+ years overall professional experience in Life Science/Pharmaceuticals/Biotech/Medical Device industries, or preferred to have similar experience in related manufacturing industries. Project Management or Program Management experience required.
Highly preferred to have prior experience at CDMO within Life Science/Pharmaceuticals/Biotech/Medical Device industries. Or preferred to have contract manufacturing environment experience in other industries.
Must be able to build consensus between customer and internal Lonza teams.
Must be able to "influence without authority" to achieve goals, and manage competing interests between various stakeholders in projects.
Technical understanding of mammalian cell culture manufacturing is ideal, but not required. Prior experience within Biologics and Mammalian Cell Culture projects in research or academic setting is helpful.
About Lonza
At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone’s ideas, big or small, have the potential to improve millions of lives, and that’s the kind of work we want you to be part of.
Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we offer equal employment opportunities to all qualified applicants regardless of race, religion, color, national origin, sex, sexual orientation, gender identity, age, disability, veteran status, or any other characteristic protected by law. If you’re ready to help turn our customers’ breakthrough ideas into viable therapies, we look forward to welcoming you on board.
Ready to shape the future of life sciences? Apply now.
Lonza is a pioneer and world leader in the CDMO industry, setting the pace with cutting-edge science, smart technology, and lean manufacturing. United by a common purpose, we turn our customers’ breakthrough innovations into viable therapies and manufacture the medicines of tomorrow.
Founded in Switzerland in 1897, our company is the first and original CDMO, and today we are more dynamic, agile and forward-focused than ever before. As one of the largest Western CDMOs, we bring together a global team of around 18,500 colleagues across five continents to deliver comprehensive, integrated solutions for our customers' complex needs.
For our customers and their patients, we bring quality, safety and reliability to bring life-enhancing and life-saving treatments to market at speed and at scale. For our colleagues, we strive to create a sense of belonging and inclusion where every person can thrive and bring their best.
