Head of Q&V and Digitalization Quality job opportunity at Roche.

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DatePosted 30+ Days Ago bot
Roche Head of Q&V and Digitalization Quality
Experience: 10-years
Pattern: full-time
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degreeBachelor's (B.A.)
loacation Shanghai, China
loacation Shanghai....China

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 Principle Roles & Responsibilities / Accountabilities Technical responsibilities Oversee and guide the technical strategy and direction of validation activities for PT Shanghai in the preparation and execution of validation protocols, including facility, utilities, equipment, cleaning, and computer system validation. Review and approve site Validation Master Plan (VMP)/project plans and ensure the strategy meets business and regulatory requirements.  As needed, review/approve validation protocols, engineering change orders, Standard Operation Procedures (SOP), engineering commissioning and turnover packages. Provide input and review for site-specific and corporate validation procedures and shared practices as applicable and in accordance with the requirements set forth in the governing quality standards in partnership with Global Quality. Oversee and guide execution of the validation of tech transfer oversight, new facility expansions and construction projects. Review and approve all relevant Quality Validation and other Site documentation and ensure documentation supports a compliant state. Provide expert interpretation and application of regulatory guidelines to ensure operations, facilities and documentation meet Roche standards and regulatory requirements. ensuring that the department ensures quality oversight of the qualification and validation processes. This applies across the entire lifecycle of the processes and equipment. This includes: Plant qualification of production equipment and the entire infrastructure (pharmaceutical water, HVAC, process gases).  Validation of production, cleaning and transport processes Validation of computer systems and software (CSV), including ensuring current data integrity requirements. Oversight of product and process transfers from or to other locations and partners Other activities assigned. Leadership responsibilities Establish and lead a competitive team to ensure the delivery and good performance through strong team work and shared responsibilities Create an environment of strong team spirit, timely and effective communications, sense of urgency, high motivation and inspire teams to achieve goals in the immediate and longer term.  Be an active and visible change agent, promoting flexible and open mindsets to new opportunities. As a leader within the Quality Leadership team, drive network activities and alignment, cross-functional planning, and decision making. Qualification and Experience Education/Qualifications Bachelor Degree or above (Pharmacy, Pharmaceutical, bioengineering, Chemistry or other relevant discipline is preferred). Leadership Competencies Leads by example Strong leadership, teamwork and management skills Ability to effectively communicate and influence across all levels of the organization Good accountability of problem solving Empower and trust people to make decisions Discover and develop the potential in people Job Required Competencies 10 or more years' work experience in the pharmaceutical or related industry 3 or more years' people management experience 5 or more years' experience in a commercially licensed GMP facility Knowledge/Skills/Competencies Expert knowledge of Quality System, Quality Validation and QA principles, practices and standards for the pharmaceutical industry. Strong knowledge of pharmaceutical, biotechnology or medical device related product operations including local and international quality regulations. Able to think strategically and translate strategies into actionable plans. Takes responsibility, drives results, and achieves expected outcomes. Possesses strong verbal and written communication skills in both English and Chinese, and the ability to influence at all levels. Build trustful and effective collaboration relationships. 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.

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