At Lonza, we are a global leader in life sciences operating across three continents. Our success is driven by talented people working together to devise ideas that help businesses improve people's lives.
We are seeking several Senior QA Specialists who will manage projects and support our growing business in BioConjugates.
Key Responsibilities:
* Ensure production of APIs adheres to Good Manufacturing Practice (GMP) as a member of the quality assurance team (PCP Conjugates).
* Support contract manufacturing and advise members of development, production, and analytical departments on all aspects of GMP.
* Verify manufacturing documentation for conformity, change control, and investigation of deviations and out-of-specification results.
* Promote continuous improvements programs to establish effective Quality Management Systems.
* Serve as the quality contact for clients and participate in their GMP audits.
Key Requirements:
* Bachelor or Master degree in Life Sciences (e.g., microbiology, biotechnology, chemistry, or related field).
* Significant experience in the biopharmaceutical industry, preferably in a GMP area.
* Experience in customer-focused environments, managing stakeholders and their needs independently.
* First experience in project management is preferred.
* Excellent English skills for customer interaction and a good basis in German (B1 level) for daily communication with colleagues.
Our products and services have a positive impact on millions of people every day. At Lonza, we respect and protect our people and environment. Ethical achievement is essential to our success. We offer the satisfaction that comes with improving lives worldwide and making a meaningful difference.