Assistant Manager QA – QA Validation | Granules India Limited | Hyderabad, Telangana, India
Granules India Limited is inviting applications for the role of Assistant Manager QA at its Hyderabad, Telangana pharmaceutical operations. This full-time opportunity is ideal for experienced professionals with 8 to 14 years of expertise in quality assurance validation, pharmaceutical compliance systems, documentation management, validation activities, and regulated manufacturing operations. The selected candidate will oversee QA validation activities, coordinate compliance programs, manage documentation systems, and support audit readiness initiatives across manufacturing and quality departments. Candidates with expertise in GMP compliance, validation protocols, pharmaceutical documentation, and quality system management will be preferred. This role offers leadership exposure to pharmaceutical quality operations, validation systems, and regulatory compliance activities within a professionally managed pharmaceutical manufacturing environment focused on operational excellence, product quality, and continuous improvement.
Location
Hyderabad, Telangana, IndiaEmployment Type
Full-timeExperience Required
8 to 14Compensation & Benefits
Competitive managerial compensation package with leadership exposure, pharmaceutical quality system responsibilities, and long-term career advancement opportunities.About Granules India Limited
Granules India Limited is a pharmaceutical organization engaged in regulated manufacturing operations, healthcare product development, and quality-focused industrial systems.Position Overview
The Assistant Manager QA will manage validation activities, quality assurance operations, compliance systems, and pharmaceutical documentation management.Key Responsibilities
- Manage QA validation activities and compliance programs.
- Review validation protocols and quality documentation.
- Coordinate with manufacturing and quality teams.
- Support audit readiness and inspection activities.
- Monitor compliance with GMP and regulatory standards.
- Maintain validation records and quality systems.
- Assist in investigation of quality observations and deviations.
- Prepare reports related to validation and compliance activities.
- Support implementation of quality improvement initiatives.
- Ensure adherence to pharmaceutical quality procedures.
Required Skills & Competencies
- Strong knowledge of QA validation systems.
- Understanding of GMP and pharmaceutical regulations.
- Leadership and coordination abilities.
- Strong documentation and analytical skills.
- Communication and reporting expertise.
- Problem-solving and compliance management capabilities.
- Attention to detail and quality accuracy.
- Ability to manage pharmaceutical documentation systems.
- Team collaboration and operational discipline.
- Capability to work in regulated pharmaceutical environments.