Executive - Production QMS – Production | Curefox Healthcare Pvt Ltd | Ahmedabad, Gujarat, India
Curefox Healthcare Pvt Ltd is inviting applications for the position of Executive - Production QMS at its pharmaceutical operations located in Ahmedabad, Gujarat, India. This full-time opportunity is suitable for candidates with 2 to 4 years of experience in pharmaceutical production systems, quality management systems, GMP compliance, documentation control, batch manufacturing coordination, and regulated production operations. The selected candidate will support production quality systems, maintain manufacturing documentation, coordinate with quality assurance teams, monitor compliance procedures, and ensure adherence to pharmaceutical operational standards. Candidates having expertise in QMS documentation, deviation handling, SOP management, pharmaceutical compliance systems, and production coordination activities will be preferred. This role offers valuable exposure to pharmaceutical manufacturing technologies, quality-driven operational systems, GMP-regulated environments, and continuous improvement practices focused on documentation accuracy, production efficiency, compliance management, and operational excellence.
Location
Ahmedabad, Gujarat, IndiaEmployment Type
Full-timeExperience Required
2 to 4Compensation & Benefits
Competitive salary package with pharmaceutical QMS exposure, production coordination opportunities, and long-term career growth.About Curefox Healthcare Pvt Ltd
Curefox Healthcare Pvt Ltd operates in the pharmaceutical industry specializing in healthcare manufacturing, regulated production systems, and quality-focused pharmaceutical operations.Position Overview
The Executive - Production QMS will manage production quality systems, documentation activities, and pharmaceutical compliance operations.Key Responsibilities
- Maintain pharmaceutical production QMS documentation.
- Coordinate with production and quality assurance teams.
- Monitor GMP compliance and operational procedures.
- Support SOP preparation and document management activities.
- Handle deviation reporting and corrective action processes.
- Maintain batch manufacturing and operational records.
- Participate in audit preparation and compliance inspections.
- Monitor production quality systems and reporting activities.
- Support continuous improvement in production operations.
- Ensure adherence to pharmaceutical quality standards.
Required Skills & Competencies
- Strong understanding of pharmaceutical production systems.
- Knowledge of QMS documentation and GMP procedures.
- Communication and coordination abilities.
- Problem-solving and analytical thinking capabilities.
- Awareness of pharmaceutical compliance standards.
- Ability to manage documentation accurately.
- Attention to operational quality and process discipline.
- Time management and multitasking capabilities.
- Team coordination and reporting management skills.
- Adaptability to regulated pharmaceutical environments.