The actual location of this job is in Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed.
Join our Manufacturing Operations team in Visp, where you will play a key role in delivering life‑changing biopharmaceuticals. As a Bioprocess Engineer USP, you will drive operational excellence in Downstream Processing, ensuring safe, compliant, and on‑time execution of manufacturing campaigns in a state‑of‑the‑art biotech environment.
An agile career and a dynamic work culture.
An inclusive and ethical workplace.
Compensation programs that recognize high performance.
Benefits in Visp: https://bit.ly/3wjkoFi
Plan, execute, and oversee USP manufacturing campaigns, ensuring safety, quality standards, and on‑time‑in‑full delivery.
Evaluate process performance, interpret test results, troubleshoot USP equipment, and recommend solutions to operational issues.
Prepare and execute SHE, EM, operational, and cleaning risk assessments for assigned products.
Author, review, and maintain GMP‑relevant documents, SOPs, tech transfer documentation, recipes, and EBRs.
Prepare, review, and support quality records including deviations, change controls, CAPAs, and investigations.
Perform or support qualification activities for equipment, manufacturing suites, and automation systems (MES/DeltaV).
Lead USP operational readiness activities, including process validation, training, in‑process control, and other startup‑phase deliverables.
A BSc or MSc in a relevant scientific or engineering discipline with proven experience in USP manufacturing, or a candidate without an academic degree but with 7+ years of hands‑on experience in USP operations or a similar role
Solid expertise in GMP environments, USP workflows, troubleshooting, and bioprocess equipment.
Experience with MES/DeltaV recipe creation, execution, or review is a strong advantage.
Structured and proactive way of working with the ability to collaborate effectively with cross‑functional teams.
Strong communication skills and readiness to support customer audits.
Ability to lead tasks independently and contribute to continuous improvement and operational excellence.
Willingness to participate in on‑call duty/Pikett.
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 value diversity and are committed to creating an inclusive environment for all employees. 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.
