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

To gain insight and experience working in Annual Product Quality Review. APQR is responsible for verifying the consistency of the existing process, the appropriateness of current specifications for both starting materials and finished product, to highlight any trends and to identify product and process improvements.

Early Talent Program Associates are expected to perform their responsibilities. They are expected to work cross-functionally and help coordinate quality-related activities across the APQR ecosystem and with other internal partners.

The Opportunity:

• You will own your professional growth by actively building foundational experience and knowledge of regulatory roles and drug development, supported by mentorship from your colleagues
• You will be responsible for key technical tasks, including compiling Annual Product Quality Review (APQR) reports by acquiring and visualizing data, and working with stakeholders to resolve product quality issues
• You will actively engage with cross-functional teams through open communication and active listening to build trust and ensure project deliverables are completed in a timely and compliant manner
• You will apply your understanding of business processes to ensure your work aligns with the Roche organization’s vision and contributes to the overall team and company goals
• You will work independently to improve your prioritization and time management skills, actively supporting the team’s objectives and ensuring high-quality, on-time project deliverables

Who You Are:

• You must hold an undergraduate degree in a life science-related field and be a recent graduate (within two years of completion) of a relevant postgraduate program
• Maximum 1 year relevant pharmaceutical experience post last degree
• You should have a strong understanding of drug manufacturing processes for both small and large molecules, as well as experience with related documentation and IT platforms like You are expected to have a deep knowledge of global pharmaceutical regulations (GMPs), Roche standards, and quality management processes within a manufacturing environment
• You must demonstrate strong critical thinking and analytical skills, including proficiency in applying statistical principles to interpret and analyze scientific data
• You must be an excellent communicator, fluent in English, with a proven ability to lead and influence cross-functional teams to resolve complex issues without formal authority
• You should be proactive in building relationships and comfortable working with diverse, global teams. Proficiency in an additional language like German is preferred
• You are expected to operate with a lean and agile mindset, drive continuous improvement, and mentor other colleagues and stakeholders on business operations and processes

This position is not eligible for relocation support. #RocheCanadaEiC 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.