(Senior) MSAT Expert Drug Product
Today, Lonza is a global leader in life sciences operating across three continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of.
For Drug Product Services (DPS), our successful Contract Development and Manufacturing Organization (CDMO) branch we have exciting opportunities. Become part of a group that enables its customers to meet some of the greatest challenges in patient treatment and join us by applying for the position as Senior MSAT Expert Drug Product.
Work as Senior MSAT expert on capital investment projects constructing and commissioning manufacturing units
Implement manufacturing processes in the plant and participate in GMP risk analysis of those
Act as Drug Product manufacturing process approver for external and internal customers as well as lead change controls and deviations
Enable success during technology transfers by applying formal processes and tools to manage transfers of information, process risks and change control
Communicate, negotiate and collaborate with customers as well as handle drop-ins from clinical facilities and clients
Lead preparation, review and approval of validation master plan and perform Qualification and Validation activities in compliance with cGMP regulations and specification requirements
Write, review, approve and execute Qualification / Validation protocols (OQ, PQ) as well as third party generated protocols and reports
Provide regular updates on qualification activities and performance
Contribute to the development and implementation of standardized MSAT procedures and processes as member / lead of cross functional teams
Responsible for continuous improvement of process performance and product quality
Act as mentor and link for scientific and production staff in different fields of expertise between Drug Product Services (DPS Basel), Quality Control and Visp Drug Product manufacturing
Take care of process monitoring and process control strategy as well as complex data analysis
University degree in Pharmaceutical Technology, Chemistry, Process Engineering or equivalent
Significant work experience and proven process understanding in Sterile Manufacturing (Pharma, regulatory aspects)
Very good communication and interaction skills with various interfaces among customers and the project organization
Experience in leading cross-functional project teams
Structured, focused and well-organized working attitude
Fluency in English and German
Green belt certification preferred
Every day, Lonza’s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.
People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.