Switzerland, Basel
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, located in Basel, Switzerland, 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 ing for the position as Senior Technology Transfer Lead DPS. Are you ready for your next challenge? now!

KEY REQUIREMENTS:

• Ph.D. or Master in pharmaceutical sciences, pharmaceutical engineering, chemistry, biochemistry, or related fields or similar qualification
• Extensive experience in biotech / pharma industry
• Knowledge of technical issues and requirements for drug product technical transfers
• Know-how in aseptic product manufacture for protein drug products desirable including lyophilization process highly desirable; manufacturing experience in prefilled syringes is an asset
• Excellent communication skills and command of English both written and oral
• Proven ability as team player and ability to lead cross-functional teams.
• Very good planning and organizing skills, including project management, risk management and technical writing skills
  On top of being an equal opportunity employer and value diversity at our company, we offer great benefits and a comprehensive relocation package for eligible talents!
  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.
  Reference: R64062

• Manage technical activities for drug product transfers from clinical development to first commercial launch of assigned projects
• Define and monitor project scope, timing and progress
• Lead setup, scale-up and implementation of the technical drug product manufacturing processes at GMP DP manufacturing site(s) and provide technical on-site support
• Responsible for process implementation and technical transfer documentation
• Drive GMP change management strategy of assigned projects as well as initiate and manage GMP change control in system
• Lead and support critical GMP product / process deviations and corresponding implementation of corrective/preventive actions (CAPAs)
• Ensure all activities are performed according to current standards (Good Manufacturing Practice (cGMP), Health Safety Environment (HSE), Regulatory, etc.)
• Enable innovation and technical strategy projects, generate IP and contribute to scientific publications and conference talks, and evaluate and implement of new methods and technologies