QMS Executive – QMS | Softgel Healthcare | Chennai, Tamil Nadu, India
Softgel Healthcare is hiring qualified professionals for the role of QMS Executive at its Chennai, Tamil Nadu pharmaceutical manufacturing facility. This full-time opportunity is suitable for candidates with 2 to 5 years of experience in quality management systems, pharmaceutical documentation, compliance monitoring, audit coordination, and regulated healthcare manufacturing operations. The selected candidate will support QMS activities, maintain quality records, coordinate internal audits, review compliance documentation, and ensure implementation of approved pharmaceutical quality procedures across manufacturing operations. Candidates with expertise in GMP documentation systems, CAPA management, deviation handling, and quality compliance practices will be preferred. This role offers valuable exposure to pharmaceutical quality systems, regulatory compliance operations, healthcare manufacturing standards, and process-driven environments focused on product quality, documentation accuracy, operational discipline, and continuous quality improvement initiatives.
Location
Chennai, Tamil Nadu, IndiaEmployment Type
Full-timeExperience Required
2 to 5Compensation & Benefits
Competitive compensation package with pharmaceutical quality systems exposure and long-term career growth opportunities.About Softgel Healthcare
Softgel Healthcare operates in the pharmaceutical manufacturing industry with expertise in healthcare production systems, quality-focused operations, and regulated pharmaceutical manufacturing processes.Position Overview
The QMS Executive will manage pharmaceutical quality management systems, compliance documentation, audit coordination, and operational quality procedures.Key Responsibilities
- Maintain quality management system documentation and records.
- Coordinate internal audits and compliance activities.
- Review deviations, CAPA, and quality reports.
- Support implementation of pharmaceutical quality procedures.
- Coordinate with production and quality departments.
- Ensure compliance with GMP and regulatory standards.
- Monitor document control and quality reporting systems.
- Support training related to QMS procedures and compliance.
- Participate in continuous quality improvement initiatives.
- Maintain operational discipline within quality systems.
Required Skills & Competencies
- Knowledge of pharmaceutical QMS and GMP systems.
- Understanding of regulatory compliance and documentation.
- Strong analytical and reporting capabilities.
- Communication and coordination skills.
- Problem-solving and process improvement expertise.
- Attention to detail and documentation discipline.
- Ability to manage quality records efficiently.
- Awareness of audit and compliance standards.
- Team collaboration and operational coordination abilities.
- Capability to work in regulated pharmaceutical facilities.