Regulatory Affairs Expert – Market Authorization

Job not on LinkedIn

🕒 January 5

Apply Now
Find Similar Remote Jobs

📊 Check your resume score for this job

Improve your chances of getting an interview by checking your resume score before you apply.

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

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

11 - 50 employees

Founded 2011

💊 Pharmaceuticals

⚕️ Healthcare Insurance

🎯 Recruiter

Pharmaceuticals • Healthcare Insurance • Recruitment

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

Apply Now

Similar Jobs

🕒 December 26, 2025

Compliance Specialist ensuring adherence to regulations in healthcare sector at Santen. Supporting the compliance culture and maintaining ethical standards in medical activities.

🗣️🇯🇵 Japanese Required

🕒 December 12, 2025

Parexel

10,000+ employees

⚕️ Healthcare Insurance

🧬 Biotechnology

💊 Pharmaceuticals

Senior Regulatory Affairs Consultant managing CMC regulatory strategies and submission processes. Collaborating with clients and ensuring compliance throughout drug development in the Japanese market.

🗣️🇯🇵 Japanese Required