Sr. Executive

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• Job details

Job Information

• Date Opened 01/09/2025
• Job Type Full time
• Work Experience 5+ years
• Industry Manufacturing
• City Pardi
• State/Province Gujarat
• Country India
• Zip/Postal Code 396191
  About Us
• MERIL
• DELIVERING WORLD-CLASS HEALTHCARE SOLUTIONS

Founded in 2006, Meril is an India-based, global medical device company that is dedicated to the innovation, design and development of novel, clinically relevant and state-of-the-art devices. Our fundamental aim is to champion the alleviation of human suffering and improve quality of life. To enable this, we are committed to R&D, innovation in manufacturing medical technology, scientific communication, and contemporary distribution avenues.

Meril was born with the aim of improving the quality of human life through innovative and advanced healthcare solutions. As a medical device manufacturer, we exist to improve the inventiveness in healthcare so that people’s lives are enriched. We continually seek excellence in providing answers to some of medicine’s toughest questions.

Meril manufactures medical solutions in the form of vascular intervention devices, orthopaedic supplements, in-vitro diagnostics, endo-surgery and ENT products. It is our core commitment to ensure the delivery of advance healthcare solutions. Our inclination towards research and development is reflected in our diverse offerings. We ensure that we adhere to the best quality of standards in manufacturing, scientific communication and distribution to deliver path-breaking healthcare products to the world.

We collaborate with physicians and global innovators to identify unmet clinical needs and develop revolutionary therapies. We encourage research and academic collaborations and remain available to interact on exciting opportunities.

Headquartered in India with a manpower of more than 4000, Meril currently conducts business in more than 100 countries. We have 100% subsidiaries in India, USA, Germany, Brazil, Russia, South Africa, Bangladesh and Turkey. We have set up operations in China and Japan too.

• Clinical Support: Provide specialized clinical support and training to healthcare professionals on medical products and procedures.
• Collaboration: Work closely with R&D teams to ensure quality and consistency of care.
• Research: Conduct Product Evaluation and clinical research activities to improve patient care and outcomes.
• Product Demonstration: Develop and deliver product demonstrations and presentations to healthcare professionals.
• Technical Support: Provide technical support and troubleshooting for medical products.
• Documentation: Maintain accurate and detailed patient records, ensuring confidentiality.
• Documentation Creation: Develop, write, and edit a variety of medical documents, including clinical study reports, regulatory submissions, research papers, and standard operating procedures (SOPs).
• Regulatory Compliance: Ensure that all documentation adheres to relevant regulatory guidelines, industry standards, and company policies.
• Collaboration: Work closely with cross-functional teams, including clinical researchers, regulatory affairs, and medical experts, to gather and interpret data and to ensure accuracy and completeness of documentation.
• Quality Assurance: Conduct thorough reviews of documents for clarity, accuracy, and consistency. Implement feedback and revisions as necessary.
• Project Management: Manage multiple writing projects simultaneously, ensuring timely delivery while maintaining high standards of quality.
• Research and Analysis: Perform comprehensive literature reviews and research to support the development of content and ensure evidence-based writing.

• Education: A bachelor’s degree in a related field such as B. Pharmacy, M. Pharmacy, Nursing, Medical Technology, or Life sciences. Advanced degrees or certifications in a Clinical Research are advantageous.
• Experience: 2-4 years previous experience in a clinical setting or a specialized medical field.
• Technical Skills: Proficiency in using medical equipment or devices and understanding medical procedures. Strong writing and editing skills with a keen attention to detail. Proficiency in medical terminology and the ability to translate complex scientific concepts into clear, accessible language.
• Knowledge: Familiarity with regulatory requirements and guidelines (e.g., ICH, FDA, EMA). Experience with clinical trial protocols and data.
• Software Proficiency: Competency in Microsoft Office Suite (Word, Excel, PowerPoint) and familiarity with reference management tools (e.g., EndNote, Zotero) and document management systems.
• Communication: Excellent verbal and written communication skills. Ability to work effectively in a team and independently.
• Organization: Strong organizational and time-management skills with the ability to handle multiple priorities and meet deadlines.

• Improved skills and experience
• Increased productivity
• Learning perspectives.
• Improved morale
• Good Connection with different teams and knowledge transfer.

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