Aspiro Pharma Limited – Specialities, a part of the renowned Hetero Group, has announced a Walk-In Drive for experienced and aspiring professionals in Quality Assurance (QA) and Environment, Health & Safety (EHS) departments. The recruitment drive is for its Injectable Manufacturing Facility located at Karkapatla, Markook, Siddipet District, Telangana.

This is an excellent opportunity for candidates seeking a career in sterile pharmaceutical manufacturing with one of India’s leading pharmaceutical organizations.

Company Overview

Aspiro Pharma Limited is a Hetero Group company known for its advanced pharmaceutical manufacturing facilities and commitment to quality, safety, and innovation. The company specializes in injectable and sterile pharmaceutical products and follows global regulatory standards.

Job Details

1. Quality Assurance (IPQA)

Position: Executive / Senior Executive
Experience: 5–10 Years
Qualification: B.Pharm / M.Pharm

Key Responsibilities:

• Shop floor IPQA monitoring and line clearance.
• BMR/BPR review.
• In-process quality monitoring.
• Qualification and validation activities.
• Compliance with GMP requirements.

2. Quality Assurance (Validation)

Position: Executive / Senior Executive
Experience: 5–10 Years
Qualification: B.Pharm / M.Pharm

Key Responsibilities:

• Equipment qualification activities.
• Utility and process validation.
• Validation protocol preparation and review.
• HVAC, water system, and cleaning validation.
• Documentation and regulatory compliance.

3. Training & Documentation

Position: Officer / Senior Officer
Experience: 3–5 Years
Qualification: B.Pharm / M.Pharm

Key Responsibilities:

• SOP preparation and documentation control.
• QA documentation management.
• Training record maintenance.
• Internal audit support.
• QMS documentation management.

4. EHS (Environment, Health & Safety)

Position: Safety Officer
Experience: 0–5 Years
Qualification: B.Tech (Chemical Engineering) / Diploma in Safety

Key Responsibilities:

• Safety inspections and audits.
• PPE compliance monitoring.
• Permit-to-Work and LOTO implementation.
• Risk assessment and hazard identification.
• Fire and emergency preparedness.
• GMP and EHS compliance.

Preferred Experience

Candidates having experience in:

• Injectable Manufacturing
• Sterile Pharmaceutical Manufacturing
• Quality Assurance Systems
• Validation Activities
• EHS Compliance

will be preferred.

Walk-In Interview Details

Company: Aspiro Pharma Limited – Specialities (Hetero Group)

Interview Date: 08 October 2026 (Thursday)

Time: 09:00 AM – 03:00 PM

Venue: Aspiro Pharma Limited – Specialities
Plot No. 5-1 & 5-6 & 5-28, Survey No. 321 & 284,
Biotech Park Phase-3, Karkapatla Village,
Markook Mandal, Siddipet, Telangana – 502281

Documents Required

Candidates should carry:

• Updated Resume
• Last 3 Months Payslips
• Experience Letter
• CTC Annexure
• Aadhaar Card
• PAN Card

Additional Benefits

• Attendance Bonus
• Production Bonus
• Night Shift Allowance
• Local Stay Allowance
• Accommodation Facility

Candidates willing to work in rotational shifts will have an added advantage during the selection process.

Unable to Attend Walk-In?

Candidates who cannot attend the interview may share their updated resumes to:

Recruitment@aspiropharma.com

Technical FAQs

1. What is IPQA in pharmaceutical manufacturing?

IPQA (In-Process Quality Assurance) ensures manufacturing activities comply with GMP standards through line clearance, process monitoring, and batch documentation review.

2. What is process validation in sterile manufacturing?

Process validation is a documented procedure that confirms a manufacturing process consistently produces products meeting predetermined quality specifications.

3. Why is HVAC validation important in injectable plants?

HVAC validation ensures controlled environmental conditions, minimizing contamination risks and maintaining sterile manufacturing standards.

4. What is LOTO in EHS?

LOTO (Lockout/Tagout) is a safety procedure used to isolate hazardous energy sources during equipment maintenance to prevent accidental startup and injuries.

5. Why is GMP compliance critical in pharmaceutical industries?

Good Manufacturing Practices (GMP) ensure product quality, patient safety, regulatory compliance, and consistency throughout the manufacturing process.