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Morunda | Pharmaceutical | Medical Device Recruiting | Japan (JPAC) Asia (APAC)
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Work with submission managers to prepare high-quality regulatory submissions (eCTD, NeeS, Paper) that meet internal and external standards.
Ensure submissions pass validation checks required by health authorities.
Lead, train, and support publishing staff (both internal and external). ( for Experienced candidates)
Help teams prepare content that’s submission-ready and meets deadlines.
Identify and manage risks that could affect submission quality or timelines.
Monitor and report project progress, daily activities, and publishing issues.
Oversee and improve publishing processes, tools, and documentation.
Act as a subject matter expert and mentor; collaborate with external partners.
Drive process improvements by analyzing current practices and suggesting changes.
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Morunda | Pharmaceutical | Medical Device Recruiting | Japan (JPAC) Asia (APAC)

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

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