Senior QA Specialist, QA Operations
📍 CH - Visp
Role and responsibilities
Represent the Quality Assurance department in cross-functional project teams and ensuring and managing interfaces to different internal and external stakeholder Assess, review and approve quality records for assigned customer projects such as deviations, change controls, CAPAs, investigations, effectiveness checks, and extensions in line with valid SOPs Author, review and approve GMP-relevant documents and SOPs in the ownership of QA Support and participate in internal and customer audits and regulatory inspections
Team / description
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.
Qualifications and Skills
Academic degree in Life Sciences (e.g. Chemistry/ Biotechnology or any related field)
Significant work experience in QA in the GMP-regulated industry
Strong communication skills for effective communication with stakeholders
Agility, resilience and flexibility, growth mindset
English language skills (written and spoken) are required, German is an advantage