Aspiro Pharma, a Unit of Hetero Group and a USFDA-approved pharmaceutical company, is conducting a Walk-In Drive for experienced professionals at its Injectable Manufacturing Facility in Karkapatla, Markook, Siddipet District, Telangana. The company is hiring candidates across Production, IPQA, QA Validations, QA Batch Release, Quality Management System (QMS), and Audit & Compliance departments. Immediate opportunities are available for professionals with 4–8 years of experience in sterile injectable manufacturing.
Company Details
| Particulars | Details |
|---|---|
| Company | Aspiro Pharma (A Unit of Hetero Group) |
| Industry | Pharmaceuticals |
| Facility | Injectable Manufacturing Facility |
| Employment Type | Full-Time |
| Work Location | Karkapatla Village, Markook Mandal, Siddipet District, Telangana |
Open Positions
| Department | Position | Qualification | Experience |
|---|---|---|---|
| Production – Vial Filling Operators | Officer / Sr. Officer / Operator / Sr. Operator | B.Sc., ITI, B.Pharm, Diploma (Any Stream) | 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 |
| Quality Management System (QMS) | Officer / Sr. Officer / Executive / Sr. Executive | B.Pharm / M.Pharm / M.Sc. | 4–8 Years |
| Audit & Compliance | Officer / Sr. Officer / Executive / Sr. Executive | B.Pharm / M.Pharm / M.Sc. | 4–8 Years |
Job Responsibilities
Production – Vial Filling Operators
- Perform aseptic vial filling machine setup and operations.
- Execute line clearance, IPC activities, and equipment cleaning.
- Maintain cGMP compliance and GDP documentation.
- Support sterile injectable manufacturing processes.
Quality Assurance – IPQA
- Conduct in-process quality assurance for injectable products.
- Perform line clearance and batch record review.
- Review IPC, environmental monitoring, and cleaning records.
- Ensure compliance with cGMP and SOPs.
- Coordinate with Production, QC, and Engineering teams.
- Handle deviations and CAPA documentation.
QA Validations
- Execute and review media fill activities.
- Perform equipment qualification (DQ, IQ, OQ, PQ) and requalification.
- Conduct process validation, cleaning validation, and hold-time studies.
- Validate utility systems including HVAC, purified water, steam, and water systems.
- Review validation protocols and reports.
- Ensure compliance with cGMP, regulatory guidelines, and data integrity.
QA Batch Release
- Review and approve Batch Manufacturing Records (BMR).
- Verify Certificates of Analysis (COA), specifications, and analytical results.
- Ensure compliance with GMP and regulatory requirements.
- Coordinate with QC, Production, IPQA, and Warehouse teams.
- Manage batch disposition and product release activities within the QMS.
Quality Management System (QMS)
- Manage QMS activities, SOPs, and document control.
- Handle change control, CAPA, and deviation management.
- Support audits and regulatory inspections.
- Conduct training management and maintain training records.
- Ensure data integrity and continuous quality improvement.
- Coordinate QMS compliance across departments.
Audit & Compliance
- Conduct internal audits covering GMP, QMS, and audit planning.
- Support regulatory inspections by USFDA, WHO, and other agencies.
- Manage audit observations, tracking, and closure.
- Participate in supplier and vendor audits.
- Ensure regulatory compliance and maintain quality documentation.
- Prepare audit reports, trend analysis, and management review inputs.
Eligibility Criteria
| Criteria | Details |
|---|---|
| Qualification | ITI, Diploma, B.Sc., B.Pharm, M.Pharm, M.Sc. (as per role) |
| Experience | 4–8 Years |
| Industry Preference | Sterile Injectable / Pharmaceutical Manufacturing |
Walk-In Interview Details
| Details | Information |
|---|---|
| Interview Date | 02 August 2026 (Sunday) |
| Interview Time | 09:00 AM – 03:00 PM |
| Interview Venue | Hetero Labs Ltd. – Corporate Office, 7-2-A2, Sanath Nagar Industrial Estate, Sanath Nagar, Hyderabad, Telangana – 500018 |
| Work Location | Karkapatla Village, Markook Mandal, Siddipet District, Telangana |
Employee Benefits
- Aseptic Allowance
- Night Shift Allowance
- Local Stay Allowance
- Attendance Allowance
- All Allowances as per Hetero Group Policy
- Hostel Facility (Accommodation provided as per company policy)
Documents to Carry
Candidates should bring:
- Updated Resume
- Last 3 Months’ Salary Slips
- Last Bank Statement
- Current CTC Annexure
- Latest Increment Letter
- Educational Certificates
- Experience Certificates
- Aadhaar Card and PAN Card Copies
Contact Details
| Details | Information |
|---|---|
| Resume Email | naresh.a@hetero.com |
| Interview Venue | Hetero Labs Ltd. – Corporate Office, Sanath Nagar, Hyderabad |
Why Join Aspiro Pharma?
- Join a USFDA-approved sterile injectable manufacturing facility.
- Work with one of the fastest-growing companies in the Hetero Group.
- Attractive allowances and company-sponsored accommodation as per policy.
- Exposure to advanced aseptic manufacturing and quality systems.
- Excellent career growth opportunities in Production and Quality Assurance.
How to Apply
Interested and eligible candidates can directly attend the Walk-In Drive on 02 August 2026 (Sunday) from 09:00 AM to 03:00 PM at Hetero Labs Ltd. – Corporate Office, Sanath Nagar, Hyderabad. Candidates should carry an updated resume, educational and experience certificates, latest increment letter, salary slips, bank statement, current CTC annexure, Aadhaar and PAN card copies. Candidates who are unable to attend the interview may send their updated resume to naresh.a@hetero.com for future consideration.
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