Roche Posted October 23, 2026

Quality Assurance Expert

Shanghai, Shanghai, China's Mainland Full time
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Roche is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

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

Objectives and Scope of Position:

●       Strategy/Execution Ratio: You will operate with a balanced focus between strategy and execution (50% Strategy / 50% Execution), driving long-term goals and executing business processes.

●       Design and deliver Quality Strategies and conclusions for assigned entities/processes.

●       Contribute to the delivery of PDQ work and the development of PDQ processes.

●       Lead and participate in PDQ goals and initiatives and support regulatory authority inspections.

●       Apply a risk-based approach to Quality Assurance strategies based on the Critical to Quality (CtQ)  framework.

●       Mentor and support the development of Quality Leads within the team.

Summary of Main Responsibilities:

●       Design and Implementation of Quality Strategies

○        Establish relationships with business stakeholders and lead the development of molecule/product/process/affiliate-level approaches with appropriate measures (CtQ Factors).

○        Analyze quality data to identify trends and risks, providing insights to business partners.

●       Delivery of Activities to Assess Quality Status

○        Lead and perform complex audits and quality assessments.

○        Synthesize individual audit issues into systematic conclusions and present findings and associated risks to senior stakeholders, ensuring quality data fulfills regulatory requirements and supports organizational goals.

●       Demonstration of Implementation to Health Authorities

○        Play a lead role in inspection preparation and management.

○        Provide training to staff and ensure relevant materials are prepared for regulatory review.

●       Execution of PDQ Goals

○        Lead assigned goals and initiatives and drive the development or revision of PDQ processes.

Networking:

●       Maintain and influence partnerships with senior business stakeholders and PDQ domains.

●       Facilitate cross-functional collaboration to ensure quality standards are met globally.

Compliance:

●       Expert knowledge in GxP regulations (NMPA, ICH guidance) and internal policies.

●       Ensure all activities are conducted in compliance with regulatory and company requirements.

Qualification, knowledge and experience:

Minimum Qualification :

●       Bachelor’s degree or equivalent in a scientific or quality-related field. Advanced degree preferred.

Minimum Experience / Knowledge:

●       Significant experience in the pharmaceutical / biotech / medical device industry, including knowledge of the end to end development and operationalisation of products, and the associated GxP regulations and considerations (e.g., GCP, IVD/MD Regulations).

●       Bachelor’s degree or equivalent in a scientific or quality-related field or equivalent combination of education, training, and experience.

●       Advanced degree in referenced fields preferred.

●       Extensive experience in leading GxP audits and managing complex quality projects.

●       In-depth knowledge of drug development processes and global regulatory landscapes.

●       Good understanding of Information Systems, e.g., audit management and analysis reporting tools.

●       Understanding of business operations and strategies.

●       Fluency in written and spoken English; bi or multi-lingual skills are desirable.

Personal competencies:

●       Strong digital and data literacy

●       Skilled in using and analyzing data to drive solutions.

●       Advanced communication and presentation skills.

●       Strong stakeholder management and engagement skills.

●       Comfortable working with ambiguous and complex information and able to synthesize it into clear and concise points of view to influence decision-making and action-taking.

●       Ability to influence with and without authority, and negotiate effective solutions.

●       Proven critical thinking, analytical, problem-solving, and decision-making skills.

●       Ability to work effectively in an international, multicultural matrix organization and as part of agile project teams. Demonstrates effective teamwork and collaboration skills.

●       Agile and creative in designing analytical solutions.

●       Experienced in leading global project teams, and strong project management skills.

●       Strong organizational and execution skills, and demonstrated ability to work independently and proactively.

●       Proven leadership and mentoring abilities.

 

 

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.

Job details

Seniority
Not listed
Function
Quality
Therapeutic area
Not listed
Location
Shanghai, Shanghai, China's Mainland
Employment type
Full time

How this role compares

Computed from every other active Quality role in our database, not just this employer's listings.

We currently track 1502 comparable Quality roles across 147 biopharma companies.

1502Comparable roles tracked
1357Currently active
147Companies hiring similar roles
54Countries represented

Salary context

261 of 1502 peers report a salary range (USD, annualized)

Peers share this role's job function. This posting doesn't list a seniority level, so peers aren't narrowed by seniority either -- the range below may span more levels than usual.

This roleSubject Not listed on this posting
Lowest disclosed · QC Lab Technician (Lilly Contractor - Fixed Term) · Lilly $13/hr – $29/hr (≈ $26,998–$60,507/yr)
Highest disclosed · VP, Quality Assurance · City Therapeutics $340,000/yr – $360,000/yr
Peer group range $43,753 – $350,000 (median $123,250)

Where these roles are based

Top locations among the 1502 comparable roles

United States589
Ireland88
Germany72
China71
France67
India57

+ 48 more countries

Seniority mix

731 of 1502 peers have a known seniority level

Manager223
Senior189
Intern/Fellow/Postdoc98
Associate65
Director46
Associate Director45
Principal33
Senior Director25
Executive/VP7

Therapeutic area mix

3 of 1502 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Vaccines & Infectious Disease2
Respiratory1

Similar opportunities

The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

40%similar
Novartis Beijing (Beijing), China Senior Director
Same function Same country
40%similar
Sanofi-Aventis Pharma Beijing Co Ltd Beijing, China
Same function Same country
40%similar
Sanofi-Aventis Pharma Beijing Co Ltd Beijing, China Manager
Same function Same country
40%similar
Sanofi-Aventis Pharma Beijing Co Ltd Beijing, China Manager
Same function Same country
40%similar
Sanofi-Aventis Pharma Beijing Co Ltd Beijing, China
Same function Same country
40%similar
Sanofi-Aventis Pharma Beijing Co Ltd Beijing, China
Same function Same country

Notify me about similar jobs

Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.

Or follow a whole field: get every new Quality job in China, and choose locations and companies.

How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

40%
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Function Therapeutic area Seniority Country
40%
M&S Graduate Program- IFB Quality Assurance Manager - Beijing
Sanofi-Aventis Pharma Beijing Co Ltd · Beijing, China · Manager
Function Therapeutic area Seniority Country
40%
M&S - Quality Assurance Manager-IFB
Sanofi-Aventis Pharma Beijing Co Ltd · Beijing, China · Manager
Function Therapeutic area Seniority Country
40%
M&S - Quality Control Expert - IFB
Sanofi-Aventis Pharma Beijing Co Ltd · Beijing, China · Seniority not listed
Function Therapeutic area Seniority Country
Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.