VI Operator/目检操作工

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. 

• Participate in new facility design and construction, including but not limited to SAT, IOPQ etc. to contribute to project delivery.
• Support VI AM for the VI kits lifecycle management.
• Participated in the implementation of VI operation readiness.
• Support the initial development and optimization of VI processes.
• Perform other duties as assigned.

• Ensure routine operation in compliance with Roche’s GMP/SHE and regulation requirements.
• Performing the following operations: e.g. Vial Visual Inspection and VI kits handling.    
• Diagnose and resolve equipment malfunctions promptly with the support of maintenance engineers to minimize downtime.
• Execute regular manufacturing operations and GMP records filling.
• Execute regular qualification activities: e.g. APS
• Ensure data accuracy, integrity, and traceability in all VI actvities.
• Implement cold chain management in the VI process.
• Related IT system operations, such as SAP, MES.
• Perform other duties as assigned.

• Senior high school and technical School (Pharmaceutical / Biological is preferred) and above.

• 3 or more years’ operation experience in the injection pharmaceutical industry, MNC Bio-pharma preferred.
• Experienced in strategic project of Visual Inspection including design, commissioning & qualification is preferred.
• Strong knowledge of cGMP and regulations relevant to the pharmaceutical industry, especially in biological industry. 
• Fluent communications skills in English is preferred and the ability to effectively communicate, collaborate, and foster positive interactions with team members and stakeholders.

#2026rochegreenfield

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.