Merck

Manager responsible for overseeing and managing all engineering and maintenance activities within a facility, ensuring production operations run smoothly, managing budgets, and fostering a culture of continuous improvement. The role requires strong leadership, project management, and regulatory compliance skills, with a focus on maintaining facilities and equipment.

The Site Digital Technology Lead is responsible for coordinating IT/OT operations at a specific site, ensuring alignment with business goals and global IT/OT strategy. This role involves managing local IT teams, driving digital transformation, implementing projects, managing budgets, and ensuring compliance with regulatory, safety, and cybersecurity requirements. The position requires experience in IT/Automation leadership, digital transformation, and stakeholder management within a matrix organization.

The Medical Science Liaison (MSL) in Oncology acts as a scientific bridge between Merck and the external medical community, engaging in scientific exchange with medical leaders. The role involves providing balanced, factual scientific information about disease areas and Company products, supporting clinical trials, and gathering scientific insights. Responsibilities include non-promotional scientific exchange, responding to unsolicited requests, facilitating clinical trials and investigator-initiated studies, and supporting the generation of local data. The role requires a PhD in a health or life science field, strong scientific knowledge, excellent communication and analytical skills, and understanding of local pharmaceutical industry guidelines and regulations.

This role is responsible for regulatory affairs in Vietnam, ensuring compliance with local regulations for company products. Key activities include preparing and submitting documentation to regulatory agencies, monitoring regulations, reviewing labeling, and acting as a pharmacovigilance contact.

This role is a Production Operator in a Fill/Finish facility, responsible for executing and monitoring production processes from material loading to finished product packaging, ensuring adherence to quality standards, safety regulations, and GMP guidelines. The position requires basic understanding of GMP and safety, at least one year of industrial manufacturing experience (preferably in pharmaceuticals), and the ability to work under pressure and perform physical tasks.

This role is responsible for embedding ethical business conduct and regulatory adherence across Human Health International (HHI) within Vietnam. It ensures local operations align with global standards, regional frameworks, and country-specific laws, acting as a trusted advisor to country leadership to enable compliant business growth and foster a culture of integrity, transparency, and accountability. Key responsibilities include business practice leadership, governance and policy implementation, risk management and monitoring, training and awareness, business partnership and advisory, due diligence oversight, and reporting.