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

Technical Job Responsibilities

● Oversee all required quality activities during the lifecycle of a GxP supplier (Source & Select,

Implement, Manage and Decommission), including but not limited to: process or method validations,

Roche audits, Health Authority inspections, complex investigations, product complaints, and

regulatory submissions, as assigned.

● Develop, negotiate and maintain Quality Agreements and Product Specific Requirements (as

appropriate) with GxP suppliers, as well as with Partners, Collaborators and External Sponsors as

applicable, and ensure compliance with agreements.

● Collaborate with GxP suppliers to address any gaps in audit responsiveness, CAPA implementation,

deviation reporting and management, complaint management, investigation closure, and change

implementation with regards to quality and timeliness with the supplier; and escalate as appropriate.

● As applicable, manage all required quality activities to support Make Assess Release (MAR) of

Roche products including approval of master process documentation, batch documentation review,

resolution of investigations, assessment of changes, and monitor and report GxP Supplier quality

performance.

● As applicable, release, reject or quarantine products (drug substance or API, bulk drug

product, and semi-finished and finished products) and medical devices produced within the area of

responsibility per applicable Roche requirements, cGMP and the schedule. Support RP and QP

Declaration and Certification requirements as applicable.

● As applicable, collaborate with GxP suppliers to maintain the manufacturing processes and the

Specifications and Analytical Methods (SAM) in a validated state and compliant with the regulatory

dossier, including stability testing programs. Also includes quality oversight for direct material

changes, certifications, supplier specifications and internal release specifications, and other

documentation.

● As applicable, develop and maintain quality risk management plans; utilize risk management tools to

identify and mitigate supplier quality and compliance risks, ensuring suppliers are in a state of

compliance.

● As applicable, manage or lead quality deliverables supporting technical transfers for manufacturing,

testing, packaging and product launches at external sites

● As applicable, engage in supplier improvement initiatives to solve complex manufacturing or quality

problems.

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.