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Roche

China Technical Regulatory (CMC) Policy Lead 

Roche is hiring a China Technical Regulatory (CMC) Policy Lead  in Beijing, China. Level rates it ; you can apply on Roche.

Level's read on this job

  • On Level's scale, this role is Little AI ●○○○: aI is not part of the work.
  • Tools and skills the posting cites include regulatory policy, stakeholder engagement and advocacy.
  • Level classifies it as a lead role.
  • Level lists 1,200+ other open roles at Roche.

AI in this role

Leads technical regulatory policy activities and external advocacy for Roche Pharma in China.

regulatory-policystakeholder-engagementadvocacycross-functional-leadership

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.


Let’s build a healthier future, together.

Roche is an Equal Opportunity Employer.

How we rate this

China Technical Regulatory (CMC) Policy Lead  at Roche rates 0 out of 100 for how much of the daily work is AI. That makes it Little AI (AI Level 1 of 4). The level is about AI in the job, not seniority.

Classification

Little AI. AI is not part of the work.

  1. ●●●● Builds AI80 to 100
  2. ●●●○ Works on AI60 to 79
  3. ●●○○ Uses AI40 to 59
  4. ●○○○ Little AI0 to 39

Levels come from how often the tools, models and workflows of the role are named in the posting itself. Read the description and count the AI tools, models and workflows it names.

Prepare for this job

Built from this posting and from similar jobs on Level.

Skills and AI tools this role asks for

Regulatory PolicyStakeholder EngagementAdvocacyCross Functional Leadership

Questions you could be asked

  1. Tell me about a project where regulatory policy was part of your work. What did you do?
  2. Tell me about a project where stakeholder engagement was part of your work. What did you do?
  3. Tell me about a project where advocacy was part of your work. What did you do?
  4. Tell me about a project where cross functional leadership was part of your work. What did you do?

Adapt your resume

  • List these exact terms on your resume: Regulatory Policy, Stakeholder Engagement, Advocacy, and Cross Functional Leadership. An applicant tracking system matches the wording, not the idea.
  • Attach one line of real, concrete experience to at least one of them. A tool named with nothing behind it rarely survives a human read.

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