Regulatory Affairs Specialist

Abbott · Bangkok, Thailand

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RegulatoryFull-timeCompany career page

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Role summary

Abbott seeks a regulatory affairs specialist for its Thailand diagnostics division to manage product registrations, submissions, and lifecycle compliance. The role involves directing regulatory submissions, engaging with agencies, and advising internal teams on regulatory strategy and manufacturing requirements.

Where this listing comes from

This listing was compiled by RoleLantern from the employer's publicly available posting on Workday, captured and rephrased by RoleLantern using automated (AI) tools on 2026-10-04 (originally posted 2026-10-04). It was not submitted or confirmed by the employer through RoleLantern. Details may be inaccurate, incomplete, outdated, or no longer available; please confirm with the employer's official posting before applying.

What they're looking for

Bachelor's degree in sciences, pharmacy, engineering, or equivalent work experience
2-3 years of regulatory affairs experience
Knowledge of local medical device regulations preferred
Fluent in local language and proficient in written and spoken English

What you'll be doing

Direct development and submission of product registration documents, supplements, amendments, and periodic reports
Liaise with regulatory agencies to expedite approval of pending product registrations
Serve as regulatory representative throughout product lifecycle to internal and external stakeholders
Advise development and marketing teams on manufacturing changes, labeling, and regulatory interpretations

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