
Hover or tap a row for full statistics (EUR / month on this chart).
Salary analysis
Compared with the selected benchmark ("All roles in Beijing, China"), this listing's salary midpoint is about 90% lower. The offer sits below the benchmark range (€9,260–€13,890). Range-width comparison is limited because one of the salary bands is incomplete. This benchmark is based on 3 comparable listings.
| Market | Lower bound (25th percentile) | Median | Upper bound (75th percentile) |
|---|---|---|---|
| All roles in Beijing, China | €9,260/per month | €13,890/per month | €13,890/per month |
| Pay in our data — not quoted in ad (Senior) | €1,158/per month | €1,158/per month | €1,158/per month |
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 The Opportunity - Provide Leadership, oversight and execution of technical regulatory policy activities for the Roche Pharma Group relevant to China including the development of Roche policy positions on key topics relevant to Pharma Technical, and effective advocacy of such positions externally. - Collaborate closely with the regulatory colleagues in China and globally to develop and execute the China regulatory policy roadmap - Ensure alignment and stakeholder engagement within Pharma Technical Operations, Product Development, Pharma International, governmental affairs as well as external interest groups Key Responsibilities and Tasks - Identify and enable regulatory policy activities in China such that Roche is globally recognized as an industry leader with health authority agencies and industry peer groups and that significant value is realized in facilitating pipeline development, marketing authorizations and excellence in manufacturing - Build and maintain relationships based on trust and respect with key health authority professionals, relevant academic and opinion leaders and non-profit scientific associations - Establish a strong partnership and networks with internal (i.e. Regulatory, Technical, Quality, Medical,, Gov. Affairs ) and external stakeholders - Ensure the development, execution and communication of the China regulatory policy roadmap - Lead strong cross-functional teams and regional/global regulatory communities of practice to drive policy change in China - Represent Roche technical regulatory policy views in China (and beyond) during external stakeholder engagement - Take leadership in local, regional and/or global associations (e.g. RDPAC, BIO, IFPMA…) and/or governmental organizations (e.g. APEC, ICH) in line with the Roche positions. - Provide leadership and consultancy to Roche Pharma Division leaders on regulatory policy and strategy related topics affecting China - Act as subject matter expert for key technical regulatory policy and strategy areas as assigned, lead the development of specified Global Regulatory Policy positions in close collaboration with SMEs. - Build influencing and advocacy knowledge and capacity and empowers other colleagues to shape the regulatory environment Core Competencies, Skills - Excellent collaboration skills - Recognized expert in relevant CMC technical/regulatory area with established external credibility as thought leader - Proven ability to build and maintain strong relationships with global health authorities - Strong team player and communicator - Creates an environment of strong team spirit, good communication, high motivation, inspire cross-functional project teams - Excellent advocacy, communication and presentation skills - Strategic thinking and analytical skills, ability to simplify complex topics and to pull it all together to strategic planning. - Challenges the status quo to drive innovation - Ability to operate successfully in a global matrix environment with shared accountability and responsibilities. Minimum Qualifications and Experience - Degree in relevant technical area ( Analytical, Biochemistry, Biology, Pharmacy) - At least 10 years of work experience in relevant area or advanced degree (PhD) in relevant technical area combined with a minimum of 5 yrs work experience - Previous experience in Regulatory (Industry or Agency) is preferred - In depth Knowledge of China regulatory environment - Previous participation and proven effectiveness in international regulatory/industry forums is highly preferred 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.
Job Details
Responsibilities
- Provide leadership and execution of technical regulatory policy activities for Roche Pharma Group in China
- Develop Roche policy positions on key Pharma Technical topics and advocate externally
- Collaborate with global and local regulatory colleagues to execute the China regulatory policy roadmap
- Ensure alignment and stakeholder engagement across Pharma Technical Operations, Product Development, and governmental affairs
- Build and maintain relationships with health authority professionals, academic leaders, and scientific associations
- Lead cross-functional teams and regulatory communities of practice to drive policy change in China
- Represent Roche technical regulatory policy views during external stakeholder engagement
- Take leadership in local, regional, and global associations (e.g., RDPAC, BIO, IFPMA) and governmental organizations (e.g., APEC, ICH)
- Provide consultancy to Roche Pharma Division leaders on regulatory policy and strategy affecting China
- Act as subject matter expert for key technical regulatory policy and strategy areas
Requirements
- Degree in relevant technical area (Analytical, Biochemistry, Biology, Pharmacy)
- At least 10 years of work experience in relevant area or PhD in relevant technical area with minimum 5 years work experience
- In depth Knowledge of China regulatory environment
- Recognized expert in relevant CMC technical/regulatory area
- Proven ability to build and maintain strong relationships with global health authorities
- Excellent advocacy, communication and presentation skills
- Strategic thinking and analytical skills
- Ability to operate in a global matrix environment
Skills & Technologies
Education Level
Bachelor
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