Granules India Limited has announced a walk-in interview opportunity for experienced pharmaceutical professionals in Quality Assurance, CQA, Operational QMS, and MSAT departments. Candidates with relevant OSD formulation experience and qualifications such as B.Pharm, M.Pharm, B.Sc, and M.Sc can attend the interview at the Hyderabad facility.
This recruitment drive offers excellent career growth opportunities for professionals looking to work with one of India’s leading pharmaceutical manufacturing companies.
Job Overview
Company Name: Granules India Limited
Job Role: Officer / Executive / Assistant Manager
Interview Date: 26 June 2026
Interview Time: 10:00 AM to 1:00 PM
Job Location: Gagillapur, Hyderabad, Telangana
Experience Required: 4 to 8 Years
Qualification: B.Pharm, M.Pharm, B.Sc, M.Sc
Department: QA (Validation), CQA, Operational QMS, MSAT
Interview Venue
Granules India Limited
Gagillapur, Hyderabad – 500043
Telangana, India
Available Positions
- QA (Validation)
Role: Executive / Assistant Manager
Qualification: B.Pharm / M.Pharm / M.Sc
Experience: 5 – 8 Years
Required Skills:
• Cleaning Validation
• Equipment Validation
- CQA
Role: Executive / Assistant Manager
Qualification: B.Pharm / M.Pharm / M.Sc
Experience: 5 – 8 Years
Required Skills:
• Internal Audits
• Gemba Audits
• Data Integrity Audits
• Vendor Qualification
• Quality Management Systems (QMS)
- Operational QMS
Role: Executive / Assistant Manager
Qualification: B.Pharm / M.Pharm / M.Sc
Experience: 5 – 8 Years
Required Skills:
• OOT and OOS Investigations
• Deviations Management
• Change Control
• CAPA Management
• BMR Review
• SOP Preparation
- MSAT
Role: Officer / Executive
Qualification: B.Sc / B.Pharm / M.Pharm / M.Sc
Experience: 4 – 6 Years
Required Skills:
• Operation and Cleaning of Manufacturing Equipment
• OSD Formulation Knowledge
• Batch Record Handling
• Manufacturing Documentation
Roles and Responsibilities
• Ensure compliance with GMP and regulatory guidelines.
• Execute validation activities and documentation.
• Conduct audits and quality system reviews.
• Manage deviations, CAPA, change controls, and investigations.
• Support manufacturing operations and process improvements.
• Maintain accurate records and regulatory documentation.
• Coordinate with cross-functional teams to ensure quality standards.
Required Qualifications
• B.Pharm
• M.Pharm
• B.Sc
• M.Sc
Candidates must possess relevant experience in pharmaceutical manufacturing and quality systems. Only candidates with OSD formulation experience are eligible to attend the interview.
Salary and Benefits
Expected Salary Range: ₹6.0 LPA – ₹14.0 LPA (Based on experience, skills, and company evaluation)
Benefits may include:
• Performance-based growth opportunities
• Health and insurance benefits as per company policy
• Learning and development programs
• Exposure to advanced pharmaceutical manufacturing systems
• Career progression within a reputed pharma organization
Documents Required
Candidates should carry photocopies of:
• Updated Resume
• Latest Increment Letter
• Last 3 Months Payslips of Current Organization
• Previous Organization Relieving and Service Certificates
• Educational Documents
• Aadhaar Card
• PAN Card
Important Instructions
• Candidates should be willing to work in shift operations.
• Spot offers may be provided to selected candidates subject to successful document verification.
• Only candidates with OSD formulation experience should attend the interview.
How to Apply
Eligible candidates can directly attend the walk-in interview on 26 June 2026 at the specified venue along with all required documents. Candidates are advised to reach the venue before the scheduled interview time for smooth registration and screening.
