Production, QA, QMS, Audit & Complicance

Aspiro Pharma, a unit of the Hetero Group and a USFDA-approved pharmaceutical company, is conducting a walk-in recruitment drive for experienced professionals to join its Injectable Manufacturing Facility in Telangana. The company is expanding its injectable operations and is looking for candidates with experience in production and quality functions.

Company

Aspiro Pharma (A Unit of Hetero Group)

Industry

Pharmaceuticals – Injectable Manufacturing

Positions Available

1. Production – Vial Filling

Designation

• Officer

• Sr. Officer

• Operator

• Sr. Operator

Qualification

• B.Sc.

• ITI

• B.Pharm

• Diploma (Any Stream)

Experience

• 4–8 Years

Key Responsibilities

• Aseptic vial filling operations

• Machine setup and operation

• Line clearance and IPC activities

• Equipment cleaning

• cGMP compliance

• GDP documentation

• Sterile manufacturing processes

2. Quality Assurance – IPQA

Designation

• Officer

• Sr. Officer

• Executive

• Sr. Executive

Qualification

• B.Pharm

• M.Pharm

• M.Sc.

Experience

• 4–8 Years

Key Responsibilities

• In-process quality assurance of injectable products

• Line clearance and batch record review

• IPC review, environmental monitoring, and cleaning record verification

• cGMP and SOP compliance

• Documentation review and data integrity

• Coordination with Production, QC, and Engineering

• Deviation handling and CAPA follow-up

3. QA Validations

Designation

• Officer

• Sr. Officer

• Executive

• Sr. Executive

Qualification

• B.Pharm

• M.Pharm

• M.Sc.

Experience

• 4–8 Years

Key Responsibilities

• Media fill execution and review

• Equipment qualification (DQ, IQ, OQ, PQ) and requalification

• Process validation and fill simulation studies

• Cleaning validation and hold time studies

• Utility and system validation (HVAC, WFI, Steam, Water Systems)

• Validation protocol review and approval

• Documentation and data integrity

• Compliance with cGMP and regulatory guidelines

4. QA Batch Release

Designation

• Officer

• Sr. Officer

• Executive

• Sr. Executive

Qualification

• B.Pharm

• M.Pharm

• M.Sc.

Experience

• 4–8 Years

Key Responsibilities

• Review and approval of Batch Manufacturing Records (BMR)

• Review of COA, specifications, and test results

• cGMP and regulatory compliance

• Coordination with QC, Production, IPQA, and Warehouse

• Documentation review and data integrity

• Batch disposition and product release through QMS

5. Quality Management System (QMS)

Designation

• Officer

• Sr. Officer

• Executive

• Sr. Executive

Qualification

• B.Pharm

• M.Pharm

• M.Sc.

Experience

• 4–8 Years

Key Responsibilities

• QMS activities

• SOP management and document control

• Change control, CAPA, and deviation management

• Audit compliance and regulatory inspections

• Training management and effectiveness

• Data integrity and continuous improvement

• Cross-functional coordination for QMS compliance

6. Audit & Compliance

Designation

• Officer

• Sr. Officer

• Executive

• Sr. Executive

Qualification

• B.Pharm

• M.Pharm

• M.Sc.

Experience

• 4–8 Years

Key Responsibilities

• Internal audits (GMP/QMS)

• Regulatory inspection support (USFDA, WHO, etc.)

• Audit planning and execution

• Audit observation tracking and closure

• Supplier/vendor audits and qualification

• Regulatory compliance documentation

• Audit reports, trend analysis, and management review support

Walk-in Interview Details

Date

• 02 August 2026 (Sunday)

Time

• 09:00 AM – 03:00 PM

Interview Venue

Hetero Labs Ltd. – Corporate Office
7-2-A2, Sanath Nagar IE,
Sanath Nagar,
Hyderabad, Telangana – 500018

Documents to Carry

• Updated Resume

• Last 3 Months' Payslips

• Bank Statement

• Present CTC Annexure

• Latest Increment Letter

• Educational Certificates

• Experience Certificates

• Aadhaar Card and PAN Card Copies

Employee Benefits

• Aseptic Allowance

• Night Shift Allowance

• Local Stay Allowance

• Attendance Allowance

• Hostel Facility (as per company policy)

• Other benefits as per Hetero Group policy

Note: This opportunity is intended for experienced professionals with 4–8 years of relevant experience in injectable pharmaceutical manufacturing.