Boehringer Ingelheim Posted October 28, 2026

Head of QC - Biopharma (Shanghai, China)

Shanghai, China Type not listed
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Boehringer Ingelheim 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

About Biopharmaceutical Contract Manufacturing

Boehringer Ingelheim aims to become China's first international provider of biopharmaceutical contract manufacturing solutions with all-round services to its clients in China and all over the world. As the leader in biopharma CMO manufacturing, Boehringer Ingelheim introduces innovative business models into China to further promote development of China's biopharma industry, boosting global competitiveness of Chinese biopharma companies, and facilitating clinical research and market launch of China's innovative medicines in a bid to accelerate growth of China's bio-technology industry. The Company's state-of-the-art production platform, management system and global biopharma network will help bio-medicines made by Chinese companies to enter the global markets.

Job Responsibilities:

As the Head of Quality Control for China Biopharmaceutical Business, lead and manage the strategic, operational performance and budget management of the Quality Control at Biopharma Shanghai, ensuring the successful delivery of business strategy, QC relevant KPIs, whilst adhering to regulatory GMP compliance.

- Develop and implement the QC strategy, to ensure it meets the business requirements and customer deliverables, as well as ensuring the QC performance against goals.

- Successfully transfer QC methods from analytical development to BI Biopharma Shanghai QC, State -of-the-art qualification and (re)-validation of analytical methods required for DS, DP, raw material, excipients and packaging materials testing.

- Review and approve certificate of analysis, test protocols and stability studies of biopharmaceutical drug substances and drug products according to global BI standards and in line with local Chinese as well as relevant international GMP standards.

- Ensure successful and efficient management of projects within Biopharma China accordingly to defined project plans and timelines (time/capacities/Cost).

- Support analytical and quality control strategies for successful clinical trail authorizations in China, in line with SFDA requirements.

- Leading the Quality Control Organization considering BI's leadership principles. Identification, hiring and development of Quality staff according to BI's talent management principles.

Job Requirements:

-More than 10 years of relevant experience if QC in pharmaceutical industry. At least 3 years experience in leading QC organization with strong scientific, regulatory and compliance background is a prerequisite.

- A good background in biological analytical testing specially in protein and Microbiological, as well as expertise in analytical method validation and method transfer. An excellent knowledge of GMP, ICH, USP and global compendia regulations and GMP guidance's, particularly as related to quality control.

- Have been engaged in sterile products quality management. Thorough understanding of applicable laws, regulations, and regulatory requirements related to pharmaceutical quality management is required.

- Strong leadership and the ability to motivate employees, forms strong and diverse teams of people with multiple perspectives and talents.

- Strategic thinking, business orientation, strong communication and negotiation skills, and fast decision-making abilities.

-Good command of both oral and written English and Chinese.

Job details

Seniority
Not listed
Function
Quality
Therapeutic area
Not listed
Location
Shanghai, China
Employment type
Not listed

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.

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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%
Senior Director, Sterility Assurance
Novartis · Beijing (Beijing), China · Senior Director
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.