QMS Senior Executive – Quality Assurance | Radicon Laboratories Ltd | Greater Noida, Uttar Pradesh, India
Radicon Laboratories Ltd is inviting experienced pharmaceutical professionals for the role of QMS Senior Executive at its Greater Noida, Uttar Pradesh facility. This full-time opportunity is ideal for candidates with 6 to 10 years of experience in quality management systems, pharmaceutical compliance, audit coordination, deviation handling, and documentation control within regulated manufacturing environments. The selected candidate will support QMS implementation, coordinate quality documentation activities, manage CAPA systems, participate in internal audits, and ensure compliance with pharmaceutical quality standards. Candidates with expertise in GMP documentation, compliance systems, quality investigations, SOP management, and pharmaceutical quality operations will be preferred. This role offers valuable exposure to regulated pharmaceutical operations, quality assurance systems, audit-driven environments, and compliance-focused manufacturing operations aimed at operational excellence, product quality, regulatory adherence, and continuous quality improvement initiatives.
Location
Greater Noida, Uttar Pradesh, IndiaEmployment Type
Full-timeExperience Required
6 to 10Compensation & Benefits
Competitive compensation package with exposure to pharmaceutical quality systems and long-term career growth opportunities.About Radicon Laboratories Ltd
Radicon Laboratories Ltd operates in the pharmaceutical industry with expertise in regulated healthcare manufacturing, quality systems management, and compliance-focused pharmaceutical operations.Position Overview
The QMS Senior Executive will manage pharmaceutical quality systems, compliance documentation, audit activities, and quality process coordination.Key Responsibilities
- Maintain quality management system documentation and records.
- Coordinate internal audits and compliance activities.
- Manage CAPA, deviations, and quality investigations.
- Ensure compliance with GMP and regulatory standards.
- Review SOPs, protocols, and quality documentation.
- Coordinate with production and quality departments.
- Support training related to quality systems and compliance.
- Monitor document control and quality reporting systems.
- Participate in continuous quality improvement programs.
- Maintain operational discipline within pharmaceutical quality systems.
Required Skills & Competencies
- Strong knowledge of pharmaceutical QMS and GMP systems.
- Understanding of regulatory compliance and documentation standards.
- Analytical and problem-solving abilities.
- Communication and cross-functional coordination skills.
- Attention to detail and documentation accuracy.
- Knowledge of audit management and CAPA systems.
- Ability to manage compliance activities efficiently.
- Awareness of pharmaceutical quality standards.
- Team collaboration and reporting capabilities.
- Capability to work in regulated manufacturing environments.