Executive

Responsibilities

• Develop and write clinical evaluation reports (CER) for pre- and post-market medical devices.
• Organize and evaluate large amounts of scientific, clinical, and medical data to create coherent and convincing CERs.
• Manage the CER writing process by planning, identifying, appraising, and analyzing clinical data.
• Ensure quality compliance by following internal and external SOPs, Work Instructions, and templates.
• Acquire, interpret, and analyze clinical data from trials, literature, and clinical experiences.
• Communicate scientific content in a clear and concise manner.
• Assist with other clinical, regulatory, quality, and engineering projects as assigned.

Requirements

• Bachelor's, Master's, or PhD in a scientific discipline.
• At least 3+ years of CER writing experience with solid knowledge of Med Dev 2.7/1, rev 4.
• At least 3+ years of experience in clinical, regulatory, quality, or engineering roles.
• Strong written and oral communication skills.
• Advanced proficiency in Microsoft Office (Word, Excel, PowerPoint).
• Demonstrated ability to manage projects, multitask, and prioritize tasks to meet deadlines.
• Ability to read, analyze, and implement complex regulations, standards, and guidance.
• Ability to work independently and interact productively with corporate executives and research sites.

Benefits

• Enhanced skills and expertise through professional development.
• Opportunities for knowledge transfer and a broadened professional network.
• A diverse and inclusive work environment.
• Improved morale and increased productivity.

About the Company

Founded in 2006, Meril is a global medical device company dedicated to the innovation, design, and development of state-of-the-art healthcare solutions. We aim to alleviate human suffering and improve quality of life through advanced R&D and manufacturing. Meril operates in over 100 countries, providing solutions in vascular intervention, orthopaedics, in-vitro diagnostics, endo-surgery, and ENT products.