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

Primary Purpose of Job (Job Summary)

Responsible for producing innovative oral-solid medicine by interfacing with highly automated production systems and controls in cGMP manufacturing environment, and maintain areas in high state of inspection preparedness. Managing operates production equipment for Xeloda/Cellcept that may include process monitoring, sampling, environment monitoring and semi-manufactures transfer operations. Maintains records and clean room environment to comply with regulatory requirements utilizing current Good Manufacturing Practices (cGMP), Roche PQS,  Standard Operating Procedures (SOP). Responsible for being proficient in functional areas and applies expert knowledge of mechanical, scientific principles, processes and pharmaceutical processing equipment.

Principle Roles & Responsibilities / Accountabilities

Lead manufacturing to implement cGMP in order to guarantee the quality of products and performance according to Roche standards. By reinforcing and monitoring obedience to national and company’s regulation or policy.Working with MSAT closely to prepare solutions for the production process, and continues operational improvement.Work with coworkers and supervisor to effectively troubleshoot equipment and process issues.Understand the theory, concepts, and regulations behind pharm technology and processes. And Provide strong knowledge of manufacturing department with an understanding of E2E process impact.Anticipates potential problems and takes preventative action. Requires judgment to know when it is necessary to consult with support groups.Trouble shooting for process problems. Understands how own actions impact others and uses this information in decision-making.Review documentation and check all calculations.Comply with safety requirements, cGMP, SOP and manufacturing documentation. Exhibit detail oriented documentation skills.Cooperate with Technical support team Operate automated systems for equipment operation. Assemble and prepare equipment for production.Set up professional interpersonal team. Communicate effectively and ability to work in a team environment.Follows established safety and environmental guidelines and procedures for all work performed. Immediately reports safety and environmental incidents including injuries, illnesses, near misses, and safety suggestions.Provide coaching and training on best practices and compliance to SOPs.Participate in the respective projects.  Participate in and support the projects including but not limited to IQ, OQ, PQ, etc. with high independency and competence.Execute the projects and implement the projects.Related SAP, MES and CHRIS system operation.

Education/Qualifications

Bachelor or abovePharmaceutical technology or relevant fields

Leadership Competencies

Models IntegrityFocus on value and customerAlign for successDeliver results Learn for the future

Job Required Competencies

5 years’ experience in Pharmaceutical industry3 years’ experience in pharmaceutical manufacturing.Excellent oral and written communication skills.Capable of writing detailed reports and summaries.Must possess high level of automation and technical process knowledge as related to prep and process within area of responsibility.Familiarity of computer-based systems.Strong ability in organization and coordinationStrong sense of GMPGood team management skillLanguage skills – English & Chinese

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 China consists of the full value chain of Pharmaceuticals and Diagnostics fields, from early research, clinical development, manufacturing to commercialization. With more than 7,000 employees, Roche China is now working to develop itself into Roche's third global strategic center after Basel and San Francisco, and making sustained efforts to fulfill its long-term commitment to China, so as to meet Chinese patients’ unmet needs.

Roche is an Equal Opportunity Employer.