Senior Officer QA

Job Listing

Job details

• Job Information
• Date Opened 10/14/2026
• Job Type Full time
• Work Experience 1-3 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.

Job Description

0-2 year experience in Medical Device/Pharma industry.

Job

Responsibility

• Monitoring of qualification and validation activities.
• Preparation of technical files and related documentation.
• Preparation and review of qualification & validation protocols and reports.
• Review of raw data, including analytical reports, BMRs, job cards, batch release certificates, data mapping reports, etc.
• Support validation activities across multiple manufacturing segments

Requirements

• Qualification & Validation (IQ/OQ/PQ)

• Technical Documentation & Technical File Preparation

• Protocol and Report Preparation & Review

• Data Review & Documentation Verification

• GMP Compliance & Regulatory Documentation

• Batch Manufacturing Records (BMR) & Analytical Report Review

• Cross-functional Coordination & Validation Support

• I'm interested

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