QA Expert Compliance 80-100% (f/m/d) - 4 months fix-term contract

Today, Lonza is a global leader in life sciences operating across five continents. 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.

The actual location of this job is in Basel or Stein, Switzerland!

Join our DPS team in Basel or Stein, Switzerland for the QA Expert Compliance role.

What you’ll 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. The full list of our local tailored benefits can also be found below. Benefits in Basel: https://bit.ly/3HZNGv2  

What you’ll do:

Supporting establishment and maintenance of the Quality Management System at Drug Product Services (DPS) especially

Participation in transfer activities to new Document Management System:

• Support Admin and Department during Clean-up of Site documentation

• Support Site and Global Admin during the migration to a new System

Supporting during establishment of Customer Quality Agreements including: 

• Update of Customer QAA Navigator tool

• Management of DocuSign approval workflow for QAA updates  

• Ensure accurate integration of Customer Quality Agreement requirements into the Annual Product Quality Review (PQR) process

Executing GMP compliance activities e.g. status reporting and trending of changes, deviations, CAPAs, self-inspections, local implementation of corporate documents 

Drive clear, engaging internal communication and support cross-functional team collaboration 

What we’re looking for:

• Extensive experience in administrative and operational support within a regulated environment

• Sound working experience in pharmaceutical industries  

• Experience and affinity towards working with different electronic systems and exploring new ones 

• Demonstrated ability to manage and process documentation workflows (e.g., contracts, agreements, DocuSign) 

• Excellent communication skills as well as experience as a member of cross-functional team 

• Sound knowledge of written and spoken English, basic knowledge of German 

• Open minded, self driven, independent 

• Structured working attitude 

• Likes to work in an international team and intercultural environment 

• Agile to adopt to new situations and moving targets in short period of time 

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.

Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.