Job Description

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.






• Literature search, review and analysis for Clinical Evaluation of R&D projects.
• To prepare Clinical Evaluation Report and Justification of the R&D Projects for DCGI Submission.
• Communicating with the Marketing Team for conduction product evaluation/ clinical evaluation of R&D Projects that have received manufacturing Licenses for further product feedback compilation for regulatory purpose.
• Communication with Clinical Research Department for conducting of Clinical Trials of the R&D Projects and support the CR Team in documentation.
• To compile Product Feedback after Product Evaluation and keep track of actions taken against the feedback.



• To Prepare Biologic Evaluation Report.



Requirements

• Degree in B. Pharm/ M. Pharm/ Graduate - Clinical research, Post Graduate - Clinical Research
• 1-3 years of experience
• Understanding of relevant medical terminology
• Sound working knowledge and skills relating to Microsoft Office Applications
• Good oral and written communication skills; fluency in spoken and written English
• Should work under pressure and proven ability of working to tight targets and deadlines
• Excellent organizational abilities and time management skills with the ability to effectively prioritize workload
• Ability to work co-operatively and productively as a team member as well as independently
• Strong interpersonal and relationship building skills
• Willingness to travel



Benefits


New Team member will add value and quality in pre-clinical work/ testing. Furthermore, will help in completing the task on the pre-decided timelines.

Work Experience


1-3 years
Industry


Medical Device
City


Pardi
State/Province


Gujarat
Country


India
Zip/Postal Code


396191