MSAT Process Expert (f/m/d) - Temporary

Join a Global Leader in Life Sciences

At Lonza, we are dedicated to transforming the life sciences landscape across three continents. Our approach is rooted in collaboration and innovation, with our greatest asset being our talented workforce. Together, we explore ideas that not only advance businesses but also enhance lives. We empower our team members to take ownership of their careers and contribute to impactful projects that benefit the world.

About the Opportunity

As our site in Visp, Switzerland continues to expand, we are seeking a seasoned expert in BioConjugates processes. The Protein Conjugation Plant (PCP) has established itself as a center of excellence, notably in the manufacturing of Antibody Drug Conjugates (ADC) and other BioConjugates. With a growing demand for these services, we have developed new BioConjugation suites to enhance our capabilities.

In this one-year temporary role, you will be instrumental in overseeing, supporting, and managing the life cycle of BioConjugate processes within Lonza's cutting-edge facilities. You will facilitate vital connections among various departments, including manufacturing, development, quality assurance, and control.

Benefits of Joining Us

• An agile career path within a dynamic work culture
• A collaborative environment that values teamwork and inclusivity
• Access to professional development programs to refine your skills
• An ethical framework in which all tasks adhere to pertinent procedures
• Compensation programs that reward high performance

Your Responsibilities

• Support commercial and clinical BioConjugates GMP campaigns within our Ibex® and Protein Conjugation Plant facilities
• Plan and supervise MSAT activities to ensure process efficiency, product quality, and adherence to safety and timeline requirements
• Lead troubleshooting initiatives on the manufacturing floor as needed
• Manage change control processes effectively
• Support process validation efforts
• Represent the facility during inspections and audits as a Subject Matter Expert
• Prepare for GMP clinical re-supply and commercial campaigns within a project team setting

Qualifications

• Master's or PhD, or equivalent experience, in Bioconjugation, Biotechnology, Chemical Engineering, Organic Chemistry, or related fields
• Extensive experience in Bioconjugation, biopharma manufacturing, and/or process development, particularly with BioConjugates or DSP (Mammalian or Microbial)
• Deep understanding of cGMP and bioprocess technology
• Strong communication capabilities, enabling effective interaction with customers and project teams
• Proficiency in English, with German language skills as a plus
• A creative, agile, and open-minded attitude

Impact and Responsibility

At Lonza, we take pride in the positive influence our products and services have on millions globally. We view our achievements as a privilege and a responsibility; ethical practices are paramount to our success. We cultivate an environment that invites challenges and fosters creativity, allowing you to address complex issues in life sciences while making a meaningful difference in the world.

Diversity and Inclusion

Lonza is committed to being an equal opportunity employer. We welcome all qualified individuals without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, or any other characteristic protected by law.