QC Investigator

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.

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Quality Control (QC) Basel/Kaiseraugst comprises approximately 350 employees, organized in 7 departments with subordinary structures, and is a central key point for the manufacturing of high-quality medicines. GMP Compliance is key to ensuring reliable and efficient analytics for the safety of our products and for the health of patients.

As a QC Investigator, you support the Quality Control department by taking over complex or critical deviations/investigations as well as thorough root cause analysis. You are a member of the section of QC GMP Systems and Investigation and focus on the quality KPIs and continuous improvement in that area.

In this role, you will have the chance to drive excellence in GMP compliance through the following responsibilities:

• Act as a member of the GMP Systems and Investigation section, leading and owning critical or complex deviations and investigations within the QC organization.
• Focus on quality KPIs within the QC department to ensure high standards are maintained.
• Support and lead deviation huddles, providing essential guidance for the quality control organization.
• Improve GMP compliance by proactively contributing to root cause analysis and implementing CAPA measures.
• Oversee ongoing improvement activities in the deviation and investigation area across the QC department.
• Continuously improve technical writing standards within the QC organization.
• Collaborate with diverse teams to ensure safety and reliability in all analytical processes.

You are a positive-thinking, integral, and self-reflective professional with the following qualifications:

• A degree in Life Sciences paired with 3+ years of professional experience in the pharmaceutical industry within Quality Assurance or QC testing.
• Extensive expertise in cGMP and profound knowledge of local and international GMP regulations.
• Proficiency in LPS methodology and in-depth knowledge of root cause analysis (e.g., ICP program).
• Analytical ability to evaluate complex issues independently and make results-oriented decisions.
• Excellent communication and collaboration skills in fluent German or English, with the ability to build trusting relationships across the global Roche network.

Ready for the next step? We look forward to hearing from you. Apply now to discover this exciting opportunity!

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.