Job Information

- Date Opened 09/25/2026
- Job Type Full time
- Work Experience 1-3 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.

Key Responsibilities

- Execute day-to-day manufacturing of urology medical devices.
- Prepare and maintain Batch Manufacturing Records (BMR) and production documentation.
- Ensure compliance with ISO 13485, GMP, and company Quality Management System.
- Coordinate with QA, QC, R&D;, Engineering, and Supply Chain for smooth production.
- Monitor production output, yield, rejection, and machine utilization.
- Support process validation (IQ/OQ/PQ) and manufacturing transfers from R&D.;
- Implement process improvements to enhance productivity and reduce waste.
- Ensure line clearance, traceability, and product identification throughout manufacturing.
- Participate in deviation, CAPA, NCR, and root cause investigations.




- Train operators on manufacturing procedures and valuable documentation practices.
- Maintain 5S, safety, and cleanroom discipline in production areas.

Requirements

Educational Qualification

- Bachelor's Degree in Biomedical Engineering, Mechanical Engineering, Production Engineering, or related discipline.
- Preferred: 1–5 years of experience in medical device manufacturing.

Technical Skills Required

- Medical device manufacturing processes
- ISO 13485 & GMP
- Good Documentation Practices (GDP)
- Process Validation (IQ/OQ/PQ)
- Lean Manufacturing & 5S
- Root Cause Analysis (5 Why, Fishbone)
- SAP/ERP production transactions
- Microsoft Excel & production reporting

Competencies

- Strong analytical and problem-solving ability
- Cross-functional collaboration
- Attention to detail
- Communication skills
- Ownership and accountability
- Continuous improvement mindset

Benefits

Hiring this role will provide the following benefits:

- Increase manufacturing capacity for the expanding Urology Solutions portfolio.
- Reduce production bottlenecks and improve on-time order fulfillment.
- Strengthen compliance with ISO 13485 and regulatory manufacturing requirements.
- Improve process efficiency, yield, and overall equipment utilization.
- Support successful transfer of new products from R&D; into commercial manufacturing.
- Enhance documentation accuracy and reduce deviations, NCRs, and rework.
- Enable scalable production for CE, RoW, and future global market expansion.

📌 Officer / Sr. Officer (Killa-pardi)
🏢 Meril Life Sciences
📍 Killa-pardi