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The Medical Advisor will be involved in fostering relationships with scientific KOLs, analysing and sharing emerging data with HCPs. The incumbent will also provide internal stakeholders with medical insights, develop local medical strategies and contribute to brand management. Additionally, they support medical event planning while ensuring compliance with industry regulations while assisting the clinical team in upholding company medical standards.
The Medical Reviewer, with a medical doctor background will be in a dynamic role that involves conducting medical case assessment expertise within the APAC region. This is done to assist the Global Consumer Safety Department in conveying the findings and conclusions regarding global adverse events or product and health inquiries. The incumbent will be the subject matter expert in ensuring data trend reviews and medical recommendations to stakeholders.
Are you passionate about Regulatory Affairs and driven to make an impact in the pharmaceutical industry? This RA Manager will work closely with the CEO and key stakeholders in Southeast Asia to ensure successful regulatory objectives. Your expertise will be crucial in overseeing regulatory projects.
The team lead will be ensuring compliance with regulatory requirements governing renal healthcare services. Responsibilities include developing and implementing regulatory strategies, policies and procedures to maintain adherence to local and international standards. This person will also oversee the preparation and submission of documents and applications including licenses and certifications while collaborating with cross functional departments.
The QA Director will represent the Quality function as a member of the Kamunting Leadership Team, keeping the patient at the center of everything we do. The purpose of this role is to ensure that we strive to improve the health and quality of people's lives. The QA Director will ensure that we have the appropriate people, systems, processes, and practices in place to enable the Quality Team to be effective and impactful.
The Pharmacovigilance Specialist will be the deputy Local Responsible Person for Pharmacovigilance (LPPV) on behalf of the company for regional country, mainly China. This includes ensuring compliance with the regulations set forth by the National Medical Products Administrations (NMPA) and the National Pharmaceutical Regulatory Agency (NPRA) and overseeing all pharmacovigilance (PV) activities.
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