Today, Lonza is a global leader in life sciences operating across five 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.
Location: Visp (Switzerland)
Relocation assistance is available for eligible candidates and their families, if needed.
Be a part of Lonza AG's Quality Control team as a Project Leader and make a significant impact! This is a great opportunity to be in contact with many different departments such as Quality Assurance, external customers,
production, and the QC shift team, contributing to our outstanding standards of excellence. Are you looking for an opportunity to work in a team with a great team spirit? Then apply today!
What you’ll get:
An agile career and dynamic working culture
An inclusive and ethical workplace
Compensation programs that recognize high performance
Along with competitive salaries, you’ll find a wide range of lifestyle, family and leisure benefits
What you’ll do:
Consulting on the demand of the client in elaborated project plans (timing, phasing of approach, perform possible extra preliminary investigations, deliverables, organization of documentation and quality assurance)
Coordination of projects and taking care for the technical realization of project steps during method transfer and consulting on projects after method transfer
Reporting on project progress and addressing customer concerns and partner concerns when they arise. Gathering, analyzing, and sharing project status updates and other relevant data as well at own initiative as on demand
Partner with functional areas to ensure challenges or improvements are surfaced, managed, monitored/trended and escalated as required. Encourage seamless collaboration between clients, project members, and customers
Initiation and completion of necessary process change controls, deviation and laboratory investigation reports. Creation, revision and review of cGMP documentation (SOP’s, Quality Instructions, protocols, reports…) based on a standard format related to quality control activities
Responsible for providing and organizing adequate training to QC associates in order to enhance the site level compliance cGMP knowledge. Proactive follow-up on development activities within the applicable discipline as well building up and sharing of knowledge within the QC department
Participate in project related audits
What we’re looking for :
MSc or PhD in Chemistry, Biology, or equivalent experience.
Proven analytical background (preferably with knowledge in HPLC, QC, and titration).
Familiarity with GMP regulations and standards is a plus.
Experience with LIMS, Empower, and Track wise systems is an advantage.
Strong organizational skills with the ability to push back and be assertive when necessary.
Proficient in English; German language skills are a plus.
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.
Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.