Regulatory Affairs Manager(Immunology), Korea

Benefits

Parental leave

12 weeks From the posting source

Non-birth-parent leave

12 weeks From the posting source

Family-building benefits

• Fertility benefits: Not verified
• Adoption assistance: Not verified
• Surrogacy assistance: Not verified

Mental health support

Not verified

Relocation assistance

Not verified

Childcare support

Not verified

Learning budget

Not verified

Verification

Source-linked checked May 7, 2026

Salary

Not verified

401(k) match

Reported from DOL Form 5500 industry filing (not employer-specific)

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Role

Seniority

Senior From the posting source

Schedule

Shift type

Not verified

Weekend work

Not verified

Company

Equity

Offered Verified - SEC 10-K source

Application

Cover letter

Not verified

Assessment

Not verified

Deadline

Not stated

Where they hire

State eligibility is not yet verified.

About this role

Regulatory Affairs Manager(Immunology), Korea Seoul, Seoul, Korea, republic of Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: PRIMARY OBJECTIVE: To manage the preparation of regulatory submissions of company products in order to obtain necessary regulatory approvals To provide regulatory input on regulatory matters to company personnel. This position will report to the RA Director with people management scope. CORE JOB RESPONSIBILITIES: Develop registration strategies and implement regulatory plan in accordance with strategic company objectives. Manage registration of new/line extension products, variations to marketed products to ensure regulatory approvals are achieved in accordance with Company objectives. Oversee regulatory affairs activities within the team, including regulatory submissions, approvals, and compliance. Manage safety update reports, certified product details and import permits Maintain contact with governmental officials of Korea MFDS to facilitate evaluation processes. Liaise with operations department and others to maintain product changes and ensure these comply with regulations. Review and assess product labeling, packaging, and promotional materials for compliance with relevant regulations and codes. Collaborating with cross-functional teams to identify and address regulatory compliance gaps and develop corrective

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