Executive

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Job Information

• Date Opened 03/31/2025
• Job Type Full time
• Work Experience 4-5 years
• Industry Medical Device
• 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.

Coordinate and Oversee Biocompatibility & Animal Studies: Manage biocompatibility testing and animal studies for new R&D products.

• Liaison between Labs and R&D: Serve as the main communication link between labs and the R&D team to conduct biocompatibility and animal studies.
• Strategy Development: Develop and execute strategies for biological assessments of both new and existing products for regulatory submissions.
• Vendor Management: Handle vendor selection for biocompatibility, animal studies, and bioanalytical labs, including negotiations and scope definition.
• Review Compliance Documents: Review study plans, reports, and amendments to ensure adherence to regulatory requirements.
• Biological Evaluation Plans: Prepare and review biological evaluation plans and reports in line with regulatory guidelines.
• Data Compilation for Regulatory Submissions: Compile data from non-clinical studies for submissions to regulatory bodies (DCGI, CE, and USFDA).
• Non-Clinical Study Justifications: Prepare justifications and rationales for non-clinical studies of R&D products.
• Regulatory Query Compliance: Address queries raised by regulatory bodies.
• Cost Negotiation: Negotiate lab costs to ensure cost-effectiveness and justifications for study prices.
• PR Process for Non-Clinical Studies: Initiate the PR process for non-clinical studies.
• Budget Management: Manage budgeting and obtain study approval.
• Identify New Labs: Find new certified labs for non-clinical studies to ensure cost-effectiveness, quality, and timely completion.
• Team Development: Develop and train the team to execute non-clinical studies for new R&D products.
• Preclinical Research Articles: Prepare research articles detailing preclinical studies utilizing animal models.

• Experience: 2-5 yrs. of experience of toxicology, zoology, immunology or pharmaceutical industry
• Education: M.Sc. Toxicology, MSc. Biotechnology, MSc. Zoology, B.Pharma, M.Pharm or related field.
• Skills: Strong reading, writing and communication skills.
• 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., Pub Med, Elsevier) 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.

• Increased Innovation
• Stronger Team Collaboration
• Clearer Career Pathways
• Improved Decision-Making
• Enhanced Flexibility
• Fostering a Sense of Purpose
• Greater Autonomy
• Improved Employee Retention
• Effective Conflict Resolution
• Better Risk Management
• Higher Quality of Work
• Support for Continuous Improvement
• Encouragement of Leadership Development
• Strengthened Organizational Culture
• Improved Resource Allocation

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