Introduction

Polymed (Poly Medicure Limited), one of India’s leading medical device manufacturers, has announced a hiring drive in Ahmedabad for talented professionals looking to build a career in the healthcare and medical device industry. With over 30 years of excellence in healthcare innovation, Polymed is inviting qualified candidates for positions in the Research & Development (R&D) and Quality – Regulatory Affairs departments.

This recruitment drive offers opportunities for experienced professionals who are passionate about product innovation, regulatory compliance, and healthcare technology advancement.

Company Overview

Poly Medicure Limited (Polymed) is a globally recognized medical device manufacturer specializing in the development and production of high-quality healthcare products. The company operates with a strong focus on innovation, regulatory compliance, patient safety, and international quality standards.

Official Website: www.polymedicure.com

Available Departments and Positions

1. Research & Development (R&D) – Design Role

Experience Required

1 to 6 Years

Educational Qualification

B.Tech / B.E. in Mechanical Engineering

Post Graduate Diploma in Plastic Technology

Key Responsibilities

Conduct feasibility studies, simulations, and testing activities.

Design and develop innovative medical device prototypes.

Participate in new product design and development projects.

Collaborate with cross-functional teams for product commercialization.

Support product transition from concept to manufacturing.

Technical Skills Required

Product Design & Development

Feasibility Analysis

Engineering Simulations

Prototype Development

Manufacturing Support

CAD Software Knowledge:

Creo

SolidWorks

2. Quality Department – Regulatory Affairs Role

Experience Required

5 to 10 Years

Educational Qualification

B.Pharm

M.Pharm

Key Responsibilities

Regulatory affairs documentation and compliance management.

Preparation and maintenance of technical files.

Coordination with global regulatory agencies.

Support product registration and approval processes.

Technical Skills Required

Regulatory Affairs Documentation

ISO 13485 Compliance

EU MDR (Medical Device Regulation)

US FDA Regulatory Requirements

Medical Device Industry Experience

Why Join Polymed?

Opportunity to work with a reputed medical device manufacturer.

Exposure to global healthcare regulations and standards.

Innovative work environment focused on research and development.

Career growth opportunities in medical technology.

Collaborative and technology-driven workplace.

Application Process

Interested candidates can share their updated CV with the recruitment team.

Email ID: hrd11@polymedicure.com

Candidates are advised to mention their department and current experience in the email subject line while applying.

Technical FAQs

FAQ 1: What is ISO 13485 and why is it important for Regulatory Affairs professionals?

ISO 13485 is an internationally recognized Quality Management System (QMS) standard specifically designed for medical device manufacturers. It ensures that organizations consistently meet customer and regulatory requirements while maintaining product safety and effectiveness.

FAQ 2: What is EU MDR and how does it impact medical device companies?

EU MDR (Medical Device Regulation 2017/745) is the European Union regulation governing medical devices. It imposes stricter requirements for clinical evaluation, risk management, traceability, and post-market surveillance to ensure patient safety and product effectiveness.

FAQ 3: Why are Creo and SolidWorks important for R&D engineers?

Creo and SolidWorks are industry-leading CAD software platforms used for:

3D Product Design

Engineering Simulations

Prototype Development

Manufacturing Drawings

Product Validation

These tools help engineers reduce development time and improve product quality.

FAQ 4: What role does feasibility analysis play in medical device design?

Feasibility analysis evaluates whether a product concept can be successfully developed, manufactured, and commercialized. It includes technical, economic, regulatory, and manufacturing assessments before full-scale product development begins.

FAQ 5: What are the key regulatory requirements for medical device approvals?

Medical device approvals generally require:

Risk Management Documentation

Clinical Evaluation Reports

Design Verification & Validation

Quality Management Compliance (ISO 13485)

Technical Documentation

Regulatory Submissions to agencies such as FDA and EU MDR authorities

Proper compliance ensures market approval and patient safety.

Conclusion

The Polymed Hiring Drive in Ahmedabad presents an excellent opportunity for professionals in R&D and Regulatory Affairs to join a fast-growing medical device organization. Candidates with expertise in mechanical design, product development, regulatory compliance, ISO 13485, EU MDR, and FDA requirements can significantly benefit from this career opportunity. Interested applicants should submit their updated resumes to hrd11@polymedicure.com and take the next step toward a rewarding healthcare industry career.