Team Lead Quality – CSV & Lab Systems Qualification
Lonza
Visp, CH
vor 13 Std.

Today Lonza is a global leader in life sciences. We are more than 15,000 employees in more than 100 locations around the world.

While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people.

In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of.

In order to support the strategic growth investment of the company in Visp Switzerland, we are looking for an experienced quality professional who will be in charge of leading a team responsible for the quality oversight for CSV (Computerized Systems Validation) and Lab Systems Qualification of CAPEX projects, supporting both Small Molecule and Biologics businesses.

The Team Lead Quality CSV & Lab Systems Qualification will manage a team of experienced quality professionals and be responsible to implement and manage capabilities that support the success of the assigned investment projects at our site in .

Key responsibilities :

Managing a team of QA CSV / qualification managers and specialists. Provides leadership to the Team with responsibility for all aspects of human resource management such as training, development, coaching and hiring.

Be a member of the Quality SGIE Qualification & Validation Leadership team.

Review and approve qualification and compliance documents and records.

Ensure that decisions are fully supported by global and local Quality and Regulatory.

Escalating issues in an open and timely manner and taking leadership for their resolution.

Key requirements :

Academic degree (Master or higher) in Pharmaceutical Sciences, Biochemistry, Chemistry or related field

Substantial work experience in a leadership role in Quality Assurance, Production or Engineering, in pharmaceutical industries and cGMP controlled environment.

Profound knowledge in EU and US GMP regulations relevant for audit / inspections, qualification / validation, compliance systems, as well as applicable guidelines (e.g. GAMP5).

Excellent knowledge of computer systems (e.g. TW, SAP, etc), quality tools such as risk based approaches FMEA, statistical process control, design of experiments and Six Sigma.

Strong collaborative mindset, organizational skills, ability to balance multiple priorities simultaneously, ability to solve problems, understanding details and strategic picture, providing practical solutions.

Strong verbal and written communication skills (English and German).

Every day, Lonza’s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility.

How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment.

Any success we achieve is no success at all if not achieved ethically.

People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences.

In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.

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