Compensation programs that recognize high performance.
As a member of the quality assurance team (PCP Conjugates), you will be responsible to ensure production of APIs is in accordance with Good Manufacturing Practice (GMP). You will support the contract manufacturing and advise members of development, production, and analytical departments on all aspects of GMP. You will be responsible for checking manufacturing documentation for conformity, change control, and investigation of deviations and OOS-results. You will combine regulatory awareness with an entrepreneurial mindset to achieve effective quality solutions. You will support continuous improvement programs to establish effective Quality Management Systems. In addition, you will be the quality contact for our clients and will be present during their GMP audits.
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.
