Associate Quality Lead

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.

A healthier future. It's what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the
people we love. That's what makes us Roche.

In Pharma Development Quality (PDQ) we strive for confidence in the integrity of our data and our processes and unrivaled transparency with health authorities, patients and society. Our work provides quality  leadership, know-how and partnering across Molecules (GCP), Products (Drug and/or Medical Devices), Pharma affiliates and global regulated processes.

The Associate Quality Lead role in PDQ is responsible for supporting the work of PDQ and the wider Roche/Genentech organization. 

This role contributes to the planning, delivery, and reporting of quality-focused work for the business as well as fulfills regulatory needs for the provision of quality data internally and externally.

The Opportunity

• Develop and implement quality strategies across Pharmaceutical Development and Quality (PDQ), including adopting a One Roche approach for medical compliance.

• Execute activities to assess and report on quality assurance status, ensuring effective quality governance and risk management.

• Present quality strategies and conclusions to Health Authorities, demonstrating compliance and confidence in the Quality Management System (QMS).

• Design and implement risk-based quality management approaches while delivering data-driven quality solutions to meet regulatory requirements.

• Enhance data collection, perform analysis, and provide quality insights for regulatory compliance and continuous improvement.

• Foster a culture of quality and innovation within Roche, encouraging the adoption of advanced tools and technology to optimize processes.

• Contribute to PDQ goals, partake in cross-functional compliance initiatives, oversee inclusive work environments, and complete additional tasks as required.

Who you are

• Bachelor's degree or equivalent in a scientific or quality-related field, or equivalent education, training, and experience.

• 3+ years of experience in the pharmaceutical, biotech, or medical device industry, with knowledge of product development, operationalization, and GxP regulations being advantageous.

• Proficiency in communication, presentation, digital tools, and data literacy.

• Strong organizational, execution, and independent problem-solving skills, with an understanding of critical quality factors and functional group operations.

• Demonstrated skills in analytical thinking, decision-making, and problem-solving.

• Ability to effectively engage and manage stakeholders.

Relocation benefits are not available for this posting.

We use artificial intelligence to screen, assess or select applicants for this role.

This posting is for an existing vacancy at Hoffmann-La Roche Ltd.

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.