Johnson & Johnson Posted September 21, 2026

Analyst Quality Control

Incheon, Korea, Republic of 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:

Quality Control

Job Category:

Professional

All Job Posting Locations:

Incheon, Korea, Republic of

Job Description:

General Laboratory Activity

Complies with laboratory safety requirements

Complies with laboratory related regulation and requirements

Preparation/Revision and review of GMP/GLP documents (Test method documents, Lab notes (Worksheet), Procedures)

Usage and Management of GMP document / Assure that GMP/GLP documents are properly maintained and/or archived

Internal and external audit/inspection Preparation and Response

Other laboratory Support activity (e.g., housekeeping)

( The responsibilities listed below may be assigned based on business needs, organizational priorities, and the individual's qualifications and competencies. )

QC Laboratory Test Activity

Perform QC testing in compliance with GMP and corporate requirements/procedures.

Review analytical data and test results.

Conduct and/or support laboratory investigations when issues occur.

Perform data integrity activities in accordance with applicable regulations and J&J requirements.

Utilize electronic systems (e.g., LIMS, MES, LES, Empower) for execution, review, and documentation of laboratory activities.

QC Laboratory Management

Laboratory system administration (LIMS. Empower, etc.)

Lab equipment management (Qualification (Instrument Decommissioning included), Calibration, Maintenance, etc.)

Coordinate/Document/Handling non-conformances, corrective actions (CAPAs) and changes (change control management)

Lab activities for creating a Safe Lab Environment

Accompany visitors and provide training to visitors

Manage and Review of GMP data in compliance with GMP and corporate requirements/Procedures

Keep supervisor informed of task status and issues

Complete corrective and preventative actions (CAPA) as assigned

Minimum Qualification

Minimum bachelor’s degree (in Chemistry, Chemical Engineering, Life Science, Pharmaceutical Engineering, or related fields)

Understanding of current Good Manufacturing Practices (cGMP) related to the QC laboratory and compendial (USP, EP, JP, etc.) requirements

Good Interpersonal communication and Collaboration skills

Demonstrated ability to organize and prioritize workload

Other Requirements (Preferred)

Experience in pharmaceutical industry

Experience in QC department

Required Skills:

Preferred Skills:

Analytical Reasoning, Business Behavior, Compliance Management, Continuous Improvement, Controls Compliance, Data Analysis, Execution Focus, ISO 9001, Persistence and Tenacity, Quality Control (QC), Quality Control Testing, Quality Standards, Quality Systems Documentation, Report Writing, Sample Testing, Technologically Savvy

Job details

Seniority
Not listed
Function
Quality
Therapeutic area
Not listed
Location
Incheon, Korea, Republic of
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 1008 comparable Quality roles across 129 biopharma companies.

1008Comparable roles tracked
931Currently active
129Companies hiring similar roles
48Countries represented

Salary context

189 of 1008 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 · Quality Control Technician 2 - Weekend Position · Merck KGaA $19/hr – $30/hr (≈ $39,520–$62,400/yr)
Highest disclosed · Vice President, Quality Assurance - GMP · Exelixis Inc $315,500/yr – $366,500/yr
Peer group range $50,960 – $341,000 (median $147,300)

Where these roles are based

Top locations among the 1008 comparable roles

United States325
China57
Germany54
Switzerland49
Ireland45
Belgium37

+ 42 more countries

Seniority mix

445 of 1008 peers have a known seniority level

Manager166
Senior120
Associate Director43
Director38
Associate22
Principal21
Senior Director19
Intern/Fellow/Postdoc9
Executive/VP7

Therapeutic area mix

1 of 1008 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
Johnson & Johnson Seoul, Korea, Republic of Manager
Same function Same country
40%similar
Johnson & Johnson Seoul, Korea, Republic of Senior
Same function Same country
40%similar
Johnson & Johnson Incheon, Korea, Republic of
Same function Same country
40%similar
GlaxoSmithKline Korea Limited Seoul Yongsan Tower, Korea, Republic of
Same function Same country
40%similar
Johnson & Johnson Incheon, Korea, Republic of
Same function Same country
25%similar
Lilly Indianapolis, Indiana, United States of America Associate
Same function

Matched on job function only -- seniority, specialty, and location weren't confirmed as aligned.

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.

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%
Associate Commercial Quality Manager
Johnson & Johnson · Seoul, Korea, Republic of · Manager
Function Therapeutic area Seniority Country
40%
QA Specialist (Product Release, Replacement of Maternity leave)
GlaxoSmithKline Korea Limited · Seoul Yongsan Tower, Korea, Republic of · Seniority not listed
Function Therapeutic area Seniority Country
25%
Director, Clinical Quality Assurance
AbbVie · North Chicago, IL · Director
Function Therapeutic area Seniority Country
25%
Associate Clinical Programmer - Clinical Study Data, Risk based Quality Management & Monitoring
Novartis · Barcelona Gran Vía, Spain · Associate
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.