Johnson & Johnson Posted October 14, 2026

Commercial Quality Specialist

Xian, China Full time
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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:

Xian, Shaanxi, China

Job Description:

Job Description

Perform product quality acceptance management to ensure its effective operation, including related SOP/WIs management, guide and monitor the acceptance process of 3PL logistic warehouses, issues handling arising during product acceptance process and review related records.

Perform market release activities in accordance with applicable regulations and internal quality requirements.

Perform returned goods management to ensure its effective operation, including related SOP/WIs management, guide and monitor the activities performed by of 3PL logistic warehouses and review related records.

Perform product destruction management including onsite supervision, records completion and archiving.

Perform temperature assessment management, including inbound transportation temperature assessment of imported products, response to customer temperature inquiries, and temperature excursions evaluation.

Perform product traceability management, including application and maintenance of product E‑code master data, uploading relationship mapping and outbound documents, and updating shipping label information.

Perform document and records management to ensure regulatory compliance and business continuity.

Perform distributor qualification administration including agreement signing and archiving, annual qualification documents updating and archiving.

Perform training management activities, including assignment of GxP and procedural training, monitoring training completion status, maintaining training records, supporting training effectiveness evaluation, and ensuring compliance with training requirements and quality metrics.

Support internal and external audits, regulatory inspections, and follow-up actions to ensure timely closure of observations.

Support product quality risk assessment, issue escalation, and mitigation activities.

Support GxP-related computerized systems and support system upgrades, validation, and process implementation activities.

Support digitalization initiatives and quality system transformation projects by participating in process optimization, system enhancement, data analysis, automation opportunities identification, and deployment of digital solutions to improve operational efficiency and compliance effectiveness.

Drive continuous improvement initiatives to enhance quality system effectiveness, operational efficiency, and regulatory compliance.

Perform other duties as assigned.

Required Qualification and Core Competencies

Licensed pharmacist is preferred.

A bachelor's degree or higher in pharmacy, medicine, biochemistry or a related field is required.

≥2 years’ experience in the Pharmaceutical or related industry is preferred, ideally with a mix of Quality and Compliance (GxP), Distribution Warehouse management. Quality and Compliance experience is essential.

Demonstrates strong written and verbal communication skills in both the local language and English.

Expert knowledge of Microsoft software and presentation.

Strategic thinking is required, with a focus on process improvement and optimization.

Demonstrates strong pharmaceutical products and project management skills, with the ability to manage multiple tasks. Understanding of pharmaceutical product development, qualification, manufacturing, packaging, validation, testing, release and distribution processes. Up-to-date knowledge of relevant pharmaceutical legislation and GxP.

Preferred Skills:

Audit Management, Business Behavior, Coaching, Compliance Management, Continuous Improvement, Data Analysis, Detail-Oriented, Goal Attainment, Internal Controls, Issue Escalation, Problem Solving, Process Oriented, Quality Control (QC), Quality Management Systems (QMS), Quality Standards, Regulatory Environment

Required Skills:

Preferred Skills:

Business Behavior, Compliance Management, Continuous Improvement, Data Analysis, Data Compilation, Detail-Oriented, Execution Focus, Goal Attainment, Internal Controls, Issue Escalation, Process Oriented, Quality Control (QC), Quality Management Systems (QMS), Quality Standards, Regulatory Environment, Report Writing

Job details

Seniority
Not listed
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 1523 comparable Quality roles across 149 biopharma companies.

1523Comparable roles tracked
1325Currently active
149Companies hiring similar roles
53Countries represented

Salary context

248 of 1523 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 · QA - Stat Sort Specialist · Lilly $18/hr – $35/hr (≈ $37,482–$72,592/yr)
Highest disclosed · VP, Quality Assurance · City Therapeutics $340,000/yr – $360,000/yr
Peer group range $55,037 – $350,000 (median $128,002)

Where these roles are based

Top locations among the 1523 comparable roles

United States608
Ireland86
France76
Germany76
China66
Belgium52

+ 47 more countries

Seniority mix

690 of 1523 peers have a known seniority level

Manager198
Senior179
Intern/Fellow/Postdoc94
Associate73
Associate Director40
Principal38
Director33
Senior Director28
Executive/VP7

Therapeutic area mix

1 of 1523 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Vaccines & Infectious Disease1

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
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

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%
Senior Director, Sterility Assurance
Novartis · Beijing (Beijing), China · Senior Director
Function Therapeutic area Seniority Country
40%
M&S - Regulatory Site Officer -IFB
Sanofi-Aventis Pharma Beijing Co Ltd · Beijing, China · Seniority not listed
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%
(Sr./Principal) Chemist-QC
Lilly · Suzhou, Shanghai, China · Principal
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.