About this role
The actual location of this job is in Basel Stücki, Switzerland.
What you will get
An agile career and a dynamic work culture
An inclusive and ethical workplace
Compensation programs that recognize high performance
What you will do:
Perform analytical testing within DPS Commercial QC (cGMP) for batch release and stability studies of drug products under cGMP according to existing method SOPs
Execution/review/approval of basic operational tasks in the lab (e.g mobile phase preparations, calibration of pH meter, balance check).
Document assay performance following Good Documentation Practices (GDocP) and flag relevant observations to the supervisor for further assessment
Following applicable EHS regulations
Ensuring cleanliness and tidiness in the laboratory. This includes adherence to 6S principles and to cGMP standards for audit readiness
Contributes in investigations and troubleshooting for methods and lab equipment issues by proactively driving the investigation and proposing mitigation measures.
Option to contribute to draft general documents, e.g. method SOPs, reports
What we are looking for:
Training as lab technician (e.g. EFZ, CTA) or BSc in Analytical Chemistry, Biochemistry or related field
Proven experience working in a GMP-regulated QC laboratory, with a strong focus on compendial methods as well as biologics and advanced analytical techniques
Experience with HPLC, CE-SDS, icIEF, or ELISA is a plus
In-depth understanding of cGMP, GDocP, and Data Integrity principles
Excellent written and verbal communication skills in English
About Lonza
At 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.
Innovation 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.
Ready to shape the future of life sciences? Apply now.
Other facts
About Lonza
Lonza is a pioneer and world leader in the CDMO industry, setting the pace with cutting-edge science, smart technology, and lean manufacturing. United by a common purpose, we turn our customers’ breakthrough innovations into viable therapies and manufacture the medicines of tomorrow.
Founded in Switzerland in 1897, our company is the first and original CDMO, and today we are more dynamic, agile and forward-focused than ever before. As one of the largest Western CDMOs, we bring together a global team of around 18,500 colleagues across five continents to deliver comprehensive, integrated solutions for our customers' complex needs.
For our customers and their patients, we bring quality, safety and reliability to bring life-enhancing and life-saving treatments to market at speed and at scale. For our colleagues, we strive to create a sense of belonging and inclusion where every person can thrive and bring their best.
What you'll do
- Perform analytical testing for batch release and stability studies of drug products under cGMP. Contribute to investigations and troubleshooting for methods and lab equipment issues.
Ready to join Lonza?
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