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 dedicated 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.
We are looking for a Scientist to join our QC HPLC Mammalian and mRNA team in Visp. Become part of our energetic and growing international team and take the opportunity to work on interesting projects in the rapidly developing field of Biologics.
Key responsibilities:
Investigation and management of deviations, as Lead Investigator
Root cause analysis (RCA) and CAPA implementation for project topics, and general lab topic.
Coaching and mentoring of junior QC colleagues.
QC analytical review and evaluation of results.
Technical writing and document review (test methods, APs, protocols, reports).
Quality oversight and audit readiness in GMP-regulated labs (participation in audits for assigned projects).
Support optimization of laboratory processes and workflows
Continuous improvement initiatives (Lean, 5S, Six Sigma, etc.)
Implementation, optimization, transfer and validation of analytical methods, with focus on HPLC, CE and icIEF.
Responsibility for all HPLC project related tasks and representation of HPLC team in the project team for the assigned projects.
Processing of investigations, change requests and deviations under cGMP.
Extraction and evaluation of analytical data, preparation of reports and presentations.
Preparation, review and approval of documents to ensure compliance with regulatory guidelines.
Expertise in analytical and technical issues for the assigned projects.
Key requirements:
Master or PhD in chemistry, biochemistry, biology or related field.
Minimum 5-10 years of proven experience in pharma industry.
Good understanding of GMP required.
Experience with HPLC, CE or icIEF desirable.
Ideally experience with IT systems like LIMS and CDS.
Proficient in English, German is 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 meaningful 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 significant difference.
Skills Required
- Master or PhD in chemistry, biochemistry, biology or related field
- 5-10 years proven experience in pharma industry
- Good understanding of GMP / cGMP
- Experience with HPLC, CE or icIEF
- Experience with LIMS and CDS
- Proficient in English (German a plus)
What We Do
At Lonza, we enable A Healthier World by supporting our healthcare customers on the path to commercialization. Our community of 16,000 talented employees work across a global network of more than 30 sites to deliver for our customers across the pharma, biotech and nutrition markets.
