Production Quality Control Maintenance Jobs at Graviti Pharma in Hyderabad FDA-approved OSD facility.
About the Company
Graviti Pharma Pvt. Ltd. is a reputed pharmaceutical manufacturing company operating a state-of-the-art, FDA-approved Oral Solid Dosage (OSD) facility in Hyderabad. The company is committed to high-quality manufacturing, regulatory compliance, and continuous improvement in pharmaceutical operations.
Graviti Pharma provides excellent career opportunities for freshers and experienced professionals across production, quality, and engineering functions.
Job Details
- Company Name: Graviti Pharma Pvt. Ltd.
- Job Location: Hyderabad, Telangana
- Departments: Production, Quality Control, Maintenance
- Experience Required: 0–8 Years
- Qualification: 10th, Intermediate, Diploma, B.Tech
- Job Type: Full-Time
- Hiring Mode: Walk-In Interview
- Job Status: Verified Job
- Walk-In Date: 13 January 2026
Job Description
Graviti Pharma is conducting a walk-in interview for multiple roles across Production, Quality Control, and Maintenance departments. This hiring drive is open to both freshers and experienced professionals who are looking to work in a regulated pharmaceutical manufacturing environment. Production Quality Control Maintenance Jobs
The roles are aligned with Oral Solid Dosage (OSD) operations and require candidates who are quality-focused, process-oriented, and compliant with cGMP and regulatory standards. Production Quality Control Maintenance Jobs
Available Positions & Departments
Production – Freshers
- Qualification: 10th / Intermediate
- Position Type: On Roll
- Work Area: Machine Cleaning Area only
- Experience: Freshers
Production – Experienced
- Experience Required: 3–6 Years
- Expertise: Compression & Coating Operations
- Roles: Machine Operators, Technicians
- Knowledge Required: cGMP and Documentation
Quality Control (QC)
- Experience Required: 3–6 Years
- Areas:
- Validations
- Raw Material & Packing Material
- In-Process & Finished Product Testing
- Stability Studies
- Instruments: HPLC, GC, UV, IR, Dissolution Apparatus
- Compliance: USFDA and regulatory standards
Maintenance
- Experience Required: 3–8 Years
- Areas: Process Maintenance, Utility Maintenance
- Qualification: Diploma / B.Tech
- Designation: Officer / Executive
Production Quality Control Maintenance Jobs
Key Responsibilities
- Production:
- Operate compression and coating machines
- Perform machine cleaning activities
- Follow cGMP guidelines and complete batch documentation
- Quality Control:
- Conduct analysis of raw materials, in-process, and finished products
- Perform validation and stability studies
- Handle analytical instruments and maintain compliance with USFDA norms
- Maintenance:
- Ensure smooth operation of process and utility equipment
- Perform preventive and breakdown maintenance
- Minimize downtime and support production continuity
- Production Quality Control Maintenance Jobs
Skills / Qualifications
- Relevant qualification as per department requirement
- Hands-on experience in OSD manufacturing (for experienced roles)
- Knowledge of cGMP, SOPs, and regulatory compliance
- Ability to work in shift-based manufacturing environments
- Attention to detail and commitment to quality and safety
- Freshers with strong discipline and willingness to learn are encouraged
Production Quality Control Maintenance Jobs
Benefits / Perks7
- Competitive salary based on qualification and experience
- Stable employment with an FDA-approved manufacturing facility
- Exposure to regulated pharmaceutical manufacturing processes
- Career growth opportunities in production, QC, and engineering
- Standard industry benefits as per company policy
Production Quality Control Maintenance Jobs
Why You Should Join
- Opportunity to work in an FDA-approved OSD facility
- Hiring open for both freshers and experienced professionals
- Hands-on exposure to pharma manufacturing and quality systems
- Long-term career prospects in a growing pharmaceutical company
- Professional work environment with compliance-driven culture
Production Quality Control Maintenance Jobs
FAQs
Is this walk-in open to freshers?
Yes, freshers are eligible for Production (Machine Cleaning Area).
Are experienced candidates required only for OSD roles?
Yes, experienced positions require hands-on OSD manufacturing experience.
Is this a full-time role?
Yes, all positions are full-time.
Is regulatory knowledge mandatory for QC roles?
Yes, experience with USFDA and regulatory standards is required.
Are there any gender restrictions?
Only male candidates are eligible for certain operational areas as specified.
How to Apply
Eligible candidates can directly attend the walk-in interview.
Walk-In Interview Details:
Date: 13 January 2026
Time: 10:00 AM to 3:00 PM
Venue:
Graviti Pharma Pvt. Ltd.
Lakadaram Gate, Beside Pennar Steel
Insnapur (Patancheru)
Hyderabad, Telangana, India
Documents Required:
- Updated Resume
- Educational Certificates
- Experience Letters (if applicable)
Contact Details:
Phone: 78425 16617 / 86888 55954 / 98498 54768
Email: rsconsultants2005@gmail.com
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