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Job Information
- Date Opened 04/06/2026
- 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.
Job Description
Experience: Typically 8–15 years
The QC Manager is responsible for overseeing all quality control activities related to raw materials, in-process materials, and finished medical devices to ensure compliance with regulatory standards, GMP, and internal quality systems.
Key Responsibilities
Quality Control Operations
- Manage QC testing of raw materials, in-process samples, and finished products.
- Ensure compliance with GMP, GLP, ISO standards, and regulatory guidelines.
- Review and approve QC test results and batch release documentation.
- Maintain and improve laboratory systems and testing procedures.
Documentation & Compliance
- Ensure QC documentation, SOPs, and records are properly maintained and updated.
- Review and approve change control, deviation reports, and investigation reports.
- Maintain laboratory compliance with regulatory audits and inspections.
Quality Systems
- Monitor calibration, validation, testing, and inspection activities.
- Ensure quality requirements are met during production and process control.
- Support CAPA (Corrective and Preventive Action) implementation.
Investigation & Troubleshooting
- Investigate OOS (Out of Specification) and OOT (Out of Trend) results.
- Identify root causes and implement corrective actions.
- Ensure product quality is maintained throughout manufacturing.
Team Management
- Lead and supervise QC analysts and officers.
- Provide training on SOPs, testing methods, and compliance procedures.
- Coordinate with QA, Production, and Regulatory teams.
Key Skills
- Quality systems management
- Laboratory operations
- CAPA & deviation management
- Regulatory compliance
- Documentation & audit readiness
- Team leadership
Good laboratory practices, sample panel preparation, QC lab process set up, method validations, training, performance studies
Requirements
ISO 13485, GLP, IVDR, WHO
Required Qualifications
- B.Sc / M.Sc / B.Pharm / M.Pharm or related science field
- 8–15 years experience in QC in pharma or medical devices
- Knowledge of
- GMP / GLP
- ISO 13485
- Regulatory compliance (CDSCO / FDA / CE)
- Analytical instruments and lab systems
Please fill in the following Form
https://forms.zohopublic.in/merillifesciencespvtltd688/form/QualityControlManagerCandidateApplication/formperma/zm_7oaQR_GN7VmlgGH4xsU1Tsi_cAOU-sI4NhYTkxn0
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