Enrolled student in engineering, chemistry, toxicology, food chemistry or any related life science degree
Understand business and technical concepts.
Strong interpersonal skills and the ability to communicate effectively.
Ability to maintain a keen attention to detail and manage multiple projects or tasks concurrently.
Fluent English with good written and verbal communication skills
Good MS Office especially Word, and Excel and problem-solving skills
Independent, assertive, good project management skills, and eager to learn
Responsibilities
Support Regulatory Affairs team in managing all tasks for Medical Device Directive (MDD) and Medical Device Regulation (MDR).
Create and update documentation according to MDD and MDR • Assist in project management
Assist with project planning and documentation related to technical file compliance
Assist in data collection and data management
Participate as a regulatory affair contact person in a cross-functional compliance management team. Responsibilities may include strategic planning, product documentation, as well as working with other team members to plan and coordinate project activities.
Prepare reports of findings, illustrating data graphically and translate complex findings into graphs.
Review internal data and test reports to ensure compliance
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