Johnson & Johnson Posted September 3, 2026

Commercial Quality Associate Manager

Xian, China Full time
Quality Manager
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Johnson & Johnson 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 Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.com .

As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.

Job Function:

Quality

Job Sub Function:

Customer/Commercial Quality

Job Category:

Professional

All Job Posting Locations:

Beijing, China, Xian, Shaanxi, China

Job Description:

We are seeking a highly motivated quality professional to join our China Commercial Quality organization as an Associate Manager, China Commercial Quality.

DESCRIPTION

This role plays a critical part in ensuring compliance, operational excellence, and business continuity through effective Quality Management System (QMS) governance, training and document management, digital transformation initiatives, and global project support.

The successful candidate will have the opportunity to work across local, regional, and global teams, driving quality excellence while supporting the organization's future transformation agenda through data-driven and digital solutions.

 

RESPONSIBILITIES

Quality Systems Management

Drive the implementation, maintenance, and continuous improvement of the China Commercial Quality Management System (QMS).

Ensure quality system processes remain compliant with applicable GxP regulations, company standards, and business requirements.

Support key quality processes including deviations, CAPA, change controls, audits, inspections, document management, and training compliance.

Monitor quality performance indicators and identify opportunities for improvement through trend analysis and risk-based decision making.

Digital Transformation & Innovation

Lead or support digital transformation initiatives aimed at improving compliance, data quality, operational efficiency, and user experience.

Partner with business, quality, and technology stakeholders to identify automation opportunities and process simplification initiatives.

Support computerized system lifecycle activities, including implementation, upgrades, validation, user acceptance testing (UAT), and change management.

Promote data-driven decision making by leveraging quality and operational data to support continuous improvement.

Training, Documentation & Data Governance & Data Integrity

Manage Commercial Quality training programs to ensure qualification and training compliance across the organization.

Oversee document lifecycle management, ensuring the creation, review, approval, retention, archival, and retrieval of quality documents and records in accordance with regulatory and company requirements.

Establish and maintain robust data governance practices to ensure data accuracy, consistency, completeness, traceability, and integrity across quality systems and business processes.

Ensure quality records and data comply with ALCOA+ principles and applicable regulatory requirements.

Support business continuity, inspection readiness, and regulatory compliance through effective management of quality documentation, master data, and critical business information.

Collaborate with global and local stakeholders to improve data standardization, data lifecycle management, reporting capabilities, and data governance processes.

Global & Regional Project Support

Participate in and lead local, regional, and global quality projects and transformation programs.

Collaborate with cross-functional and cross-regional stakeholders to ensure successful delivery of project objectives.

Support organizational initiatives related to digitalization, process excellence, simplification, and capability development.

Compliance & Inspection Readiness

Support investigations, root cause analysis, risk assessments, and CAPA implementation related to quality events and compliance issues.

Contribute to internal audits, external inspections, and health authority interactions.

Maintain a strong inspection readiness mindset and support sustainable compliance efforts.

Continuous Improvement

Identify opportunities to streamline processes, eliminate waste, and improve operational effectiveness using Lean and continuous improvement principles.

Foster a culture of quality, innovation, accountability, and continuous learning.

 

REQUIRED QUALIFICATIONS

Bachelor's degree or above in Pharmacy, Pharmaceutical Sciences, Life Sciences, Chemistry, Engineering, Quality Management, or a related discipline.

Minimum 5 years of experience in pharmaceutical, healthcare, medical device, or other regulated industries.

Strong experience in GMP, GDP, GSP, Quality Systems Management, Quality Operations, or Compliance functions within a multinational environment.

Demonstrated experience supporting audits, inspections, CAPA management, and quality system processes.

Strong project management and stakeholder management skills.

Excellent communication skills in both English and Chinese.

Strong analytical thinking, problem-solving ability, and learning agility.

Ability to work effectively in a global matrix organization.

Experience in document management, data governance, data integrity, and quality data management within a regulated GxP environment is highly desirable.

Good understanding of Data Integrity requirements and ALCOA+ principles and their application in quality systems, documentation, computerized systems, and quality records management.

 

PREFERRED QUALIFICATIONS

Licensed Pharmacist certification.

Experience in commercial quality or distribution quality operations.

Experience supporting or leading digital transformation initiatives.

Experience with computerized systems, system implementations, validation activities, or business process automation.

Experience with Lean, Continuous Improvement, Operational Excellence, or related methodologies.

Exposure to global or regional projects and cross-functional collaboration.

KEY COMPETENCIES

Quality Systems Leadership

Digital Mindset

Process Excellence

Data Analytics & Data Governance

Continuous Improvement

Project Management

Stakeholder Management

Change Management

Cross-functional Collaboration

Learning Agility

Strategic Thinking

Business Partnership

Required Skills:

Preferred Skills:

Audit Management, Business Savvy, Coaching, Communication, Compliance Management, Continuous Improvement, Fact-Based Decision Making, ISO 9001, Issue Escalation, Problem Solving, Quality Control (QC), Quality Management Systems (QMS), Quality Standards, Regulatory Environment, Standard Operating Procedure (SOP)

Job details

Seniority
Manager
Function
Quality
Therapeutic area
Not listed
Location
Xian, China
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 310 comparable Manager Quality roles across 81 biopharma companies.

310Comparable roles tracked
275Currently active
81Companies hiring similar roles
31Countries represented

Salary context

65 of 310 peers report a salary range (USD, annualized)

Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.

This roleSubject Not listed on this posting
Lowest disclosed · Associate Quality Control Analyst (Virology) · Regeneron Pharmaceuticals, Inc (USA) $22/hr – $34/hr (≈ $45,302–$70,699/yr)
Peer group range $58,001 – $201,900 (median $163,000)

Where these roles are based

Top locations among the 310 comparable roles

United States150
China21
Ireland17
India17
Netherlands14
Germany14

+ 25 more countries

Seniority mix

310 of 310 peers have a known seniority level

Manager197
Associate73
Associate Director40

Therapeutic area mix

0 of 310 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

No peers with a known therapeutic area yet.

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.

60%similar
Sanofi-Aventis Pharma Beijing Co Ltd Beijing, China Manager
Same function Same seniority Same country
60%similar
Sanofi-Aventis Pharma Beijing Co Ltd Beijing, China Manager
Same function Same seniority Same country
60%similar
Sanofi-Aventis Pharma Beijing Co Ltd Beijing, China Manager
Same function Same seniority Same country
60%similar
Roche Shanghai, Shanghai, China's Mainland Manager
Same function Same seniority Same country
60%similar
Roche Shanghai, Shanghai, China's Mainland Manager
Same function Same seniority Same country
60%similar
Boehringer Ingelheim 南昌, China Manager
Same function Same seniority 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.

60%
M&S Graduate Program- IFB Quality Assurance Manager - Beijing
Sanofi-Aventis Pharma Beijing Co Ltd · Beijing, China · Manager
Function Therapeutic area Seniority Country
60%
Associate Manager, QA Biologics
Roche · Shanghai, Shanghai, China's Mainland · Manager
Function Therapeutic area Seniority Country
60%
(Sr.) Manager, Quality & Compliance (Shanghai, China)
Boehringer Ingelheim · Shanghai, China · Manager
Function Therapeutic area Seniority Country
60%
Assistant QC Manager (Shanghai, China)
Boehringer Ingelheim · Shanghai, China · Manager
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.