QMS Officer – Quality Assurance | Radicon Laboratories Ltd | Greater Noida, Uttar Pradesh, India

Radicon Laboratories Ltd is inviting applications for the role of QMS Officer for its chemical manufacturing and quality systems operations in Greater Noida, Uttar Pradesh, India. This full-time opportunity is suitable for candidates with 2 to 3 years of experience in quality management systems, documentation control, audit coordination, SOP management, compliance monitoring, CAPA handling, deviation management, quality assurance systems, operational documentation, and regulatory support activities within chemical manufacturing environments.

The selected candidate will support Quality Management System operations and compliance activities across manufacturing and quality departments. Responsibilities include maintaining QMS documentation, preparing and reviewing SOPs, coordinating internal audits and quality reviews, monitoring deviation and CAPA records, supporting regulatory compliance activities, participating in quality inspections, maintaining operational reports and documentation systems, coordinating with production and quality teams, ensuring adherence to company quality procedures, and supporting continuous improvement initiatives related to quality assurance systems. Candidates should possess strong understanding of quality systems and operational compliance workflows.

This role provides valuable exposure to chemical manufacturing quality systems, operational compliance activities, audit management workflows, documentation systems, quality assurance coordination, and manufacturing operational standards within a reputed chemical organization. Professionals interested in quality assurance and QMS coordination can strengthen their technical and operational expertise through this opportunity.

Location

Greater Noida, Uttar Pradesh, India

Employment Type

Full-time

Experience Required

2 to 3

About Radicon Laboratories Ltd

Radicon Laboratories Ltd operates in the chemical industry specializing in manufacturing operations, quality systems, compliance management, and operational excellence activities.

Key Responsibilities

• Maintain quality management system documentation.
• Prepare and review SOPs and quality records.
• Coordinate internal audits and quality reviews.
• Monitor CAPA and deviation management systems.
• Support compliance and regulatory activities.
• Maintain operational reports and documentation.
• Coordinate with production and quality departments.
• Ensure adherence to quality procedures and standards.
• Participate in operational reviews and inspections.
• Support continuous improvement initiatives.

Required Skills

• Strong understanding of QMS and compliance systems.
• Knowledge of audit and documentation workflows.
• Awareness of CAPA and deviation management processes.
• Communication and coordination management expertise.
• Problem-solving and analytical thinking abilities.
• Documentation and reporting skills.
• Time management and workflow planning capabilities.
• Attention to operational accuracy and compliance.
• Team coordination and multitasking expertise.
• Adaptability to manufacturing environments.

Educational Qualification

MSC

Industry

Chemical

Why Join Radicon Laboratories Ltd?

Radicon Laboratories Ltd offers professionals opportunities to work on advanced quality systems and manufacturing operations within the chemical industry.

How to Apply

Interested candidates can apply through ACKJOBS and complete the application process for this quality assurance opportunity.

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