Technology Transfer Lead 80-100% (m/f/d) in Raron

pThe actual location of this job is in Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed. /ppThis is a fully site‑based role. Working together in person supports close, real‑time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards. /ph3What you’ll get: /h3ulliAn agile career and a dynamic work culture /liliAn inclusive and ethical workplace /liliCompensation programs that recognize high performance /li /ulpIn addition to a competitive salary, you can expect numerous lifestyle, family, and leisure benefits. The full list of our local tailored benefits can also be found below. /pulliBenefits in Visp: /li /ulpFor Drug Product Services (DPS), our successful Contract Development and Manufacturing Organization (CDMO) branch located in Visp, we have an outstanding opportunity as Technology Transfer Lead. Become part of a group that enables its customers to meet some of the greatest challenges in patient treatment! /ph3What you will do: /h3ulliLeads technical transfer activities including setup and implementation of technical manufacturing processes for sterile GMP DP manufacturing /liliManage technical activities for drug product transfers from clinical development to first commercial launch of assigned projects /liliDefine and monitor project scope, timing and progress /liliLead setup, scale-up and implementation of the technical drug product manufacturing processes at GMP DP manufacturing site(s) and provide technical on-site support /liliResponsible for process implementation and technical transfer documentation /liliDrive GMP change management strategy of assigned projects as well as initiate and manage GMP change control in system /liliLead and support critical GMP product / process deviations and corresponding implementation of corrective/preventive actions (CAPAs) /liliEnsure all activities are performed according to current standards (Good Manufacturing Practice (cGMP), Health Safety Environment (HSE), Regulatory, etc.) /liliEnable innovation and technical strategy projects, generate IP and contribute to scientific publications and conference talks, and evaluate and implement of new methods and technologies /li /ulh3What we are looking for: /h3ulliIdeally PhD. or Bachelor/ Master Degree with equivalent experience in pharmaceutical sciences, pharmaceutical engineering, chemistry, biochemistry, or related fields or similar qualification /liliExtensive experience in biotech / pharma industry /liliKnowledge of technical issues and requirements for drug product technical transfers /liliKnow-how in aseptic product manufacture for protein drug products desirable including lyophilization process, manufacturing experience in prefilled syringes is an asset /liliExcellent communication skills with great teammate attitude /liliVery good planning and organizing skills, including project management, risk management and technical writing skills /li /ulpAt 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. /ppInnovation 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. /p #J-18808-Ljbffr