Location: the actual location of this job is in Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed.
Currently we are looking for several Senior QA Specialists (f/m/d), who will work on our new growth project. As a member of a CAPEX projects Quality Project team, you will manage the QA related activities in close contact with QC, Engineering and Manufacturing to ensure the quality oversight is given. You will ensure timely delivery of project, even in the face of project requirements and priorities through excellent planning and management of the project.
Join Lonza and apply for this innovative opportunity!
What you will get:
An agile career and a dynamic work culture.
An inclusive and ethical workplace.
Compensation programs that recognize high performance.
In addition to a competitive salary, you can expect numerous lifestyle, family, and leisure benefits. Our full list of tailored local benefits can be found below.
Benefits in Visp: https://bit.ly/3wjkoFi
What you will do:Responsible for project specific QA Operation work during commissioning/qualification and project tech transfer in IBEX
Assess and manage tasks that would impact Quality operation during GMP manufacturing
Plan for future activities and coordinate with other departments (e.g. QC, Engineering, Manufacturing) to complete the planned activities
Support day-to-day Quality Assurance activities in accordance with approved SOPs/Policies for a GMP manufacturing facility
Review GMP records to ensure compliance with cGMP per written procedures
Make real-time decisions on process events on the floor, based on knowledge of defined SOPs & policies
Participate in walkthroughs and audit/inspections
Academic degree in Life Sciences or a related field
Significant experience in the pharmaceutical Quality area
Work experience in a role in Quality Assurance, Production or Engineering, in pharmaceutical industries and cGMP regulated environment
QA experience in tech transfer is preferred
Excellent knowledge of computer systems (e.g. TW, SAP, etc.) and quality tools such as risk based approaches (e.g. FMEA)
Fluent English (written&verbal) is required
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.
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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.
