Aspiro Pharma, a leading USFDA-approved pharmaceutical company with a strong global presence, is conducting a Walk-In Drive for experienced professionals at its Injectable Manufacturing Facility in Karkapatla, Siddipet, Telangana. The company is hiring candidates for Production (Vial Filling), IPQA, QA Validations, and QA Batch Release departments. Professionals with 4–8 years of experience in injectable manufacturing are invited to attend the walk-in interview.
Company Details
| Particulars | Details |
|---|---|
| Company | Aspiro Pharma Limited |
| Industry | Pharmaceuticals |
| Employment Type | Full-Time |
| Experience Required | 4–8 Years |
| Work Location | Injectable Facility, Karkapatla (V), Markook (M), Siddipet District, Telangana |
Open Positions
| Department | Designation | Qualification | Experience |
|---|---|---|---|
| Production – Vial Filling | Operator / Sr. Operator / Supervisor | Diploma, ITI, B.Sc., B.Pharmacy | 4–8 Years |
| Quality Assurance – IPQA | Officer / Sr. Officer / Executive / Sr. Executive | B.Pharm, M.Pharm, M.Sc. | 4–8 Years |
| QA Validations | Officer / Sr. Officer / Executive / Sr. Executive | B.Pharm, M.Pharm, M.Sc. | 4–8 Years |
| QA Batch Release | Officer / Sr. Officer / Executive / Sr. Executive | B.Pharm, M.Pharm, M.Sc. | 4–8 Years |
Key Responsibilities
Production – Vial Filling
- Perform aseptic vial filling operations.
- Machine setup, operation, and monitoring.
- Carry out line clearance, IPC activities, and equipment cleaning.
- Ensure cGMP compliance and GDP documentation.
- Follow sterile manufacturing processes.
Quality Assurance – IPQA
- Conduct in-process quality assurance for injectable products.
- Perform line clearance and batch record verification.
- Review IPC, environmental monitoring, and cleaning records.
- Verify compliance with cGMP and SOPs.
- Review documentation and ensure data integrity.
- Coordinate with Production, QC, and Engineering teams.
- Handle deviation investigations and CAPA follow-up.
QA Validations
- Execute equipment qualification (DQ, IQ, OQ, PQ) and requalification.
- Perform process validation (media fills, aseptic process simulations).
- Conduct cleaning validation and hold time studies.
- Validate utility and HVAC systems, purified water, and steam systems.
- Review and approve validation protocols and reports.
- Ensure validation documentation complies with cGMP and regulatory guidelines.
QA Batch Release
- Review and approve Batch Manufacturing Records (BMR).
- Review Certificates of Analysis (COA), specifications, and test results.
- Ensure compliance with cGMP and regulatory requirements.
- Coordinate with QC, Production, IPQA, and Warehouse teams.
- Maintain documentation and data integrity.
- Manage batch disposition and product release in the QMS.
Required Skills
- Injectable Manufacturing
- Aseptic Vial Filling
- cGMP & GDP Documentation
- Sterile Manufacturing
- In-Process Quality Assurance (IPQA)
- Validation (DQ, IQ, OQ, PQ)
- Batch Manufacturing Record (BMR) Review
- Batch Release
- CAPA & Deviation Handling
- SOP Compliance
- Data Integrity
- Regulatory Compliance
Walk-In Interview Details
| Details | Information |
|---|---|
| Interview Date | 30 July 2026 (Thursday) |
| Interview Time | 09:00 AM – 03:00 PM |
| Interview Venue | Aspiro Pharma Limited Specialities, Plot No. S-1 & S-6, Survey No. 321 & 284, Biotech Park Phase 3, Karkapatla, Telangana – 502279 |
Allowances & Benefits
- Aseptic Allowance
- Night Shift Allowance
- Local Stay Allowance
- Attendance Allowance
- Hostel Facility (Accommodation as per company policy)
Documents to Carry
Candidates should carry:
- Updated Resume
- Last 3 Months’ Pay Slips
- Bank Statement
- Current CTC Annexure
- Latest Increment Letter
- Educational Certificates
- Experience Certificates
- Aadhaar Card and PAN Card Copies
Unable to Attend?
Candidates who are unable to attend the walk-in drive can share their resumes via email at:
Why Join Aspiro Pharma?
- Opportunity to work with a USFDA-approved pharmaceutical organization.
- Exposure to advanced injectable manufacturing and sterile production.
- Competitive allowances and employee benefits.
- Career growth in Production and Quality Assurance functions.
- Work in a Great Place to Work® Certified organization.
How to Apply
Interested and eligible candidates can directly attend the Walk-In Drive on 30 July 2026 between 09:00 AM and 03:00 PM at Aspiro Pharma Limited Specialities, Biotech Park Phase 3, Karkapatla, Telangana. Candidates should carry all required documents for verification. Those who are unable to attend can email their updated resume to careers@aspiro.com for future opportunities.
Join our Official WhatsApp Channel Click Here