68 Medical Affairs Jobs in Malaysia | Job Vacancies | July 2026 | Ricebowl
显示68个工作的结果
"medical affairs"
不要错过任何 Medical Affairs 的新工作机会
管理提醒
SGD10,000 - SGD15,000 每月
Singapore
- Regulatory Affairs - Strategize, initiate, plan and coordinate with necessary departments including corporate regulatory affairs, trademark for regulatory submission, approval, and maintenance of licenses. Ensure the units are in compliance with Regulatory and Pharmacovigilance requirements.
- Pharmacovigilance – Ensure company safety standards are followed. To ensure the units within SEA operates in compliance with Regulatory and Pharmacovigilance requirements and ensure discussions with General Manager (GMs)/ Multiple Country Manager (CMs) with SEA to allocate resources and provide means that allow employees to fulfil their duty Work according to the company values, the business ethics, and internal laws.
- Minimum of 12 years experience with 8 years of people management in senior roles in the pharmaceutical industry. Experience in randomized controlled trials (RCTs), real-world evidence (RWE) - Observational studies, Prospective studies. ...
Posted
a month ago
Medical Communications Specialist (6 months contract) - MNC Medical Communications Specialist (6 months contract) - MNC
MICHAEL PAGE (PERSONNEL) PTE. LTD.
SGD5,000 - SGD5,000 每月
Singapore
- Assist in creating, reviewing, and localizing scientific and medical materials such as presentations, publications, digital content, and training tools
- Liaise with external partners, scientific bodies, and professional associations to support collaborative initiatives
- Translate global materials into varied formats suitable for multiple channels and audiences ...
Posted
24 days ago
Undisclosed
Singapore, Singapore
- Growth Opportunities: We offer a wealth of fulfilling challenges and growth opportunities in a fast-moving, game-changing organization.
- Identify, lead, and undertake a variety of projects across the affiliates, focusing on building a best-in-class medical affairs group.
- Lead collaboration with external experts and patient groups, and generate data through liaisons with country medical directors and their teams and cross-functional teams. ...
Posted
a month ago
Undisclosed
KL City
- Ensure consistency of medical messaging across indications, sectors (public and private), and engagement formats.
- Support scientific readiness for upcoming indications.
- Scientific Exchange and KOL Engagement ...
Posted
a month ago
Undisclosed
Hong Kong
- Provides structured and ad‑hoc medical education and scientific training to relevant internal functions in a compliant, non‑promotional manner.
- Core Job Responsibilities:
- Provide scientific and medical input to launch and cross‑functional teams (Medical, Commercial, Market Access, Regulatory) to support successful oncology brand launch, ensuring scientific accuracy, balance, and compliance with medical governance standards. ...
Posted
24 days ago
PEOPLE PROFILERS PTE. LTD.
SGD9,000 - SGD9,000 每月
Singapore
- Lead communication with critical regulators to respond to non-conformances, deficiencies, and questions.
- Develop and implement processes and procedures to maintain regulatory compliance related to medical device pre- and post-market activities involving regulatory, R&D, quality and medical affairs.
- Monitor changes in the regulatory and legislative environment. ...
Posted
16 days ago
Undisclosed
Singapore
- .Document management: Maintain and organize regulatory files (electronic and paper) for reliable tracking, retrieval, and archiving of controlled documents
- .Good Regulatory Practice (GRP): Support GRP activities and routine compliance checks to align with internal SOPs and HSA expectations
- .Operations and admin: Provide operational and administrative support for assigned RA projects and meetings ...
Posted
a month ago
MYR3,000 - MYR3,982 每月
- Develop, review, and maintain Quality Manuals, SOPs, forms and related quality documentation.
- Ensure the Quality Management System (QMS) is effectively implemented, maintained, and continuously improved in compliance with GDPMD requirements.
- Coordinate and monitor QMS activities, including document control, corrective and preventive actions (CAPA), and continuous improvement initiatives. ...
Posted
a month ago
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