Analyst Quality Control (Contract)

New roles land in Following.

Incheon, Korea, Republic ofPosted 2 days agocontract

Apply on Johnson & Johnson's career page

What you'd do

Comply with laboratory safety requirements and GMP/GLP regulations.
Prepare,revise,and review GMP/GLP documents and test methods.
Perform QC testing in compliance with GMP and corporate procedures.

What they want

Bachelor's degree in Chemistry,Chemical Engineering,Life Science,or Pharmaceutical Engineering.
Fluency in written English and conversational spoken English.
Interpersonal communication skills and ability to collaborate effectively.

Nice to have

At least 3 years of relevant experience in pharmaceutical industry.
Prior experience in QC department or pharmaceutical manufacturing.
Knowledge and understanding of current Good Manufacturing Practices (cGMP).

Seoulstart's read

Visa tier (likely): F-2 / F-4 / F-5 / F-6 holders welcome
Korean language: Korean preferred (conversational)
English friendliness: High: JD in English, foreign-friendly signals
Context: J&J Incheon facility is under preliminary closure review; fixed-term contract role carries heightened employment uncertainty and requires clarity on transition timeline and severance terms before accepting.

This is Seoulstart's analysis of the public job description, not the employer's stated policy. Verify visa sponsorship, language requirements, and remote allowances directly with the recruiter.

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