QC E2E Digital Expert (temporary 1 year)

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.

The Position

Quality Control (QC) Digital Backbone is a new section within the Quality Control Basel / Kaiseraugst organization comprising approximately 30 employees, organized in 2 teams and subject matter experts. This unit focuses on Master Data Management, Application Support, as well as BPM ( Business Process Manager) /BPO (Business Process Owner) tasks within the digital QC systems. 

As a Quality Control E2E Digital Expert, you are a member of the Master Data Management team and will be responsible for the digital systems in the Quality Control Department Basel / Kaiseraugst (e.g. SingleLIMS, ASPIRE, Speca), which is crucial to ensure compliance of our products.

The Opportunity

In this role, your responsibilities will include:

• Member of the QC Master Data Management team within the section QC Digital Backbone

• Responsible for the local Master data within the area of responsibility (SingleLIMS, ASPIRE & Speca)

• Operational support of these systems incl. Incident management, documentation, and reporting

• Harmonization of local master data between Basel, Kaiseraugst, and global interfaces

• Drive improvements in the local lab systems

• Ensuring a good flow of information within and outside your own organizational area.

• Development, implementation, and execution of QC strategies and goals with local as well as global partners

• Represent the area in audits and inspections; Ensure procedures and documentation are regulatory compliant and inspection-ready.

Who You Are

To succeed in this role, you have the following:

• Following your studies in life sciences, you have 3+ years of professional experience in the pharmaceutical industry in the field of quality assurance or quality control testing.

• Preferably experience in the area of IT systems within the pharmaceutical industry

• You are familiar with LPS methodology, have extensive expertise in cGMP, as well as profound knowledge of local and international GMP regulations.

• You take on challenging tasks independently, have the analytical ability to evaluate complex issues and make decisions.

• You have a professional and results-oriented work style and are focused on continuous improvement.

• As an integrative personality with strong communication skills, you can build trusting and effective relationships with a wide range of partners at the Kaiseraugst site and in the global Roche network.

• Your excellent communication skills in fluent German and English enable you to deal with interlocutors at all levels.

This position is fixed term for 1 year.

Excited to shape the future with us? We look forward to receiving your application!

Who we are

A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.

Let’s build a healthier future, together.

Roche is an Equal Opportunity Employer.