Regulatory Affairs Expert – Market Authorization

Job not on LinkedIn

🕒 January 5

🇯🇵 Japan – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

🚔 Compliance

👻 Ghost score 76%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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Morunda | Pharmaceutical | Medical Device Recruiting | Japan (JPAC) Asia (APAC)

WebsiteLinkedInAll Job Openings

11 - 50 employees

Founded 2011

💼 Consulting

🏥 Healthcare

📣 Marketing

Consulting • Healthcare • Marketing

Morunda is a recruitment firm specializing in connecting multinational companies within the pharmaceutical and medical device industries with top talent in Japan and Asia-Pacific. With over 75 years of combined experience, Morunda focuses on placing senior-level professionals and aiding in market entry strategies, ensuring that organizations find the right candidates to drive success in the healthcare sector.

📋 Description

• Act as the General Marketing Supervisor (GMS), overseeing Quality Assurance and Pharmacovigilance functions • Manage both pre- and post-approval GMS responsibilities with effectiveness and accountability • Develop and implement regulatory strategies for assigned pharmaceutical products • Lead the preparation and submission of regulatory documentation, including Module 1 and Application Forms for Marketing (AFM)

🎯 Requirements

• Extensive experience in regulatory affairs • Strong written and verbal communication skills • Broad understanding of related disciplines such as pharmaceutical manufacturing, pharmacovigilance, and quality assurance • Ability to evaluate complex scientific and technical data

🏖️ Benefits

• Health insurance • Flexible work arrangements