Quality Assurance / Quality Control Executive

Why This Role Matters
Quality Assurance and Quality Control are the backbone of pharmaceutical manufacturing. In regulated environments, maintaining product safety, efficacy, and compliance with global standards is critical. Professionals working in QA and QC ensure that every batch manufactured meets strict regulatory requirements, follows GMP norms, and maintains data integrity.
Aurobindo Pharma is offering a walk-in opportunity for experienced pharma professionals to join its regulated manufacturing operations. This recruitment drive provides exposure to high-standard production environments and long-term career stability within one of India’s leading pharmaceutical organizations.
For professionals with 2–6 years of experience in regulated manufacturing facilities, this role offers structured growth, technical skill enhancement, and opportunities to work within compliance-driven operations.

Job Description
Aurobindo Pharma is conducting a walk-in interview for experienced candidates in Quality Assurance (QA) and Quality Control (QC) departments at APL Health Care Limited – Unit IV, Naidupeta. Selected candidates will contribute to analytical testing, in-process quality monitoring, documentation control, validation activities, and compliance systems.
The role demands strong knowledge of GMP regulations, documentation accuracy, and regulatory readiness. Candidates should have hands-on experience in pharmaceutical manufacturing setups and a clear understanding of quality systems.

Key Features of the Role:
• Opportunity to work in a regulated manufacturing environment
• Exposure to GMP-compliant production facilities
• Hands-on experience in QA/QC systems
• Career progression within a reputed pharma company
• Learning opportunities in validation, documentation, and compliance
• Stable long-term employment prospects

Walk-In Interview Details
Date: 7th March 2026
Time: 9:00 am to 2:00 pm
Venue: APL Health Care Limited – Unit IV
Location: Menakuru SEZ, Naidupeta, Tirupati District, Andhra Pradesh, India
Candidates are advised to report early for smooth registration and carry updated resumes along with all educational and professional documents.

Available Departments & Positions
Quality Control (QC)
• IP / FP Analysis
• Stability Studies
• Nasal Formulation Testing

Quality Assurance (QA)
• IPQA Activities
• QMS Documentation
• Validation Processes
• Market Complaint Handling

Responsibilities
Quality Control
• Perform analytical testing of raw materials and finished products
• Execute stability sample analysis as per regulatory standards
• Maintain laboratory documentation and compliance records
• Ensure adherence to GMP and data integrity practices

Quality Assurance
• Monitor IPQA activities across manufacturing operations
• Handle deviation, CAPA, and change control systems
• Support validation and qualification activities
• Manage quality documentation and internal/external audits

Required Qualifications
Candidates must demonstrate hands-on industry exposure and sound knowledge of pharmaceutical quality systems. Strong documentation skills and regulatory understanding are essential.

Educational Requirements:
• B.Pharm / M.Pharm / MSc (Relevant Science Discipline)
• 2 to 6 years of pharmaceutical industry experience
• Strong understanding of GMP and regulatory compliance
• Experience in regulated manufacturing facilities preferred

Experience and Skills:
• Experience in QC analytical testing or QA documentation systems
• Knowledge of IPQA processes and validation protocols
• Familiarity with deviation, CAPA, and change control procedures
• Strong documentation accuracy and data integrity awareness
• Ability to work in a structured manufacturing environment
• Team coordination and audit readiness skills

Salary Insights
Estimated Salary Range: ₹3,00,000 – ₹7,50,000 per annum (based on experience and department).
Compensation is aligned with industry standards and may vary depending on technical expertise and role allocation. Employees benefit from structured growth pathways and learning opportunities within the organization.

Company Overview
Aurobindo Pharma is a globally recognized pharmaceutical manufacturer known for its strong regulatory compliance and manufacturing excellence. The company operates multiple USFDA, EU, and other internationally approved facilities, producing high-quality formulations across therapeutic segments.
APL Health Care Limited – Unit IV, located in Naidupeta, is one of its regulated manufacturing units supporting domestic and international markets. Working here provides professionals exposure to advanced production systems and global compliance frameworks.

FAQs

1. Is prior pharmaceutical experience mandatory?
   Yes, candidates must have 2–6 years of relevant industry experience.

2. Are freshers eligible?
   No, this walk-in drive is specifically for experienced professionals.

3. What departments are hiring?
   Quality Control and Quality Assurance departments.

4. Is experience in regulated facilities preferred?
   Yes, candidates from GMP-compliant manufacturing units are preferred.

5. What documents should candidates carry?
   Updated resume, educational certificates, experience letters, and relevant supporting documents.

Application Tips
• Revise GMP, data integrity, and regulatory compliance fundamentals
• Be prepared to discuss hands-on experience in QA/QC systems
• Carry all original and photocopy documents
• Reach the venue early for smooth registration
• Highlight validation, stability, or IPQA exposure during interviews