Quality Control Officer – Quality Control | Granules India Limited | Hyderabad, Telangana, India
Granules India Limited is conducting a walk-in hiring drive for the role of Quality Control Officer at its pharmaceutical manufacturing operations located in Hyderabad, Telangana, India. This full-time opportunity is suitable for candidates with 2 to 6 years of experience in pharmaceutical quality control, OSD formulation testing, laboratory operations, analytical testing systems, GMP compliance, and formulation manufacturing environments. The selected candidate will perform quality control testing activities, monitor laboratory operations, maintain analytical documentation systems, support OSD formulation quality processes, and ensure adherence to pharmaceutical quality standards and operational procedures. Candidates having expertise in OSD formulation quality control, laboratory instrumentation, analytical testing procedures, GMP documentation, and pharmaceutical manufacturing quality systems will be preferred. This role offers valuable exposure to modern pharmaceutical laboratory operations, analytical quality systems, formulation manufacturing environments, and quality-focused operational practices aimed at product safety, compliance excellence, laboratory efficiency, and pharmaceutical manufacturing reliability.
Location
Hyderabad, Telangana, IndiaEmployment Type
Full-timeWalk-in Information
Walk-in drive scheduled on 2026-05-17Experience Required
2 to 6Compensation & Benefits
Competitive salary package with pharmaceutical quality control exposure, laboratory operations experience, and professional career growth opportunities.About Granules India Limited
Granules India Limited operates in the pharmaceutical industry specializing in formulation manufacturing, healthcare product development, and pharmaceutical quality systems.Position Overview
The Quality Control Officer will manage laboratory testing systems, OSD formulation quality operations, and pharmaceutical analytical support activities.Key Responsibilities
- Perform pharmaceutical quality control and analytical testing activities.
- Support OSD formulation laboratory operations.
- Maintain analytical records and GMP documentation systems.
- Coordinate with production and quality assurance departments.
- Ensure compliance with pharmaceutical quality standards.
- Monitor laboratory equipment and operational efficiency.
- Support sample analysis and product quality monitoring.
- Participate in audit preparation and compliance activities.
- Maintain safety and discipline within laboratory operations.
- Support continuous improvement in quality control systems.
Required Skills & Competencies
- Strong understanding of pharmaceutical quality control systems.
- Knowledge of OSD formulation analytical operations.
- Communication and laboratory coordination abilities.
- Problem-solving and analytical thinking capabilities.
- Awareness of GMP and pharmaceutical compliance standards.
- Ability to manage laboratory workflows efficiently.
- Attention to product quality and documentation accuracy.
- Time management and multitasking capabilities.
- Team coordination and operational support skills.
- Adaptability to pharmaceutical manufacturing environments.