APL walk-in QA & QC Executives

APL HealthCare QA QC Jobs | MPharm Andhra

APL HealthCare hiring QA & QC Executives with 2–8 years experience in Naidupeta, Andhra Pradesh. Eligible for M.Sc, B.Pharm, M.Pharm.

APL HealthCare Limited, a part of the Aurobindo group, has announced a walk-in interview drive for experienced pharmaceutical professionals in the Quality Assurance and Quality Control departments at its Unit IV facility located in Naidupeta, Tirupati District, Andhra Pradesh.

This latest pharma hiring notification is creating strong interest among candidates searching for pharmaceutical QA jobs, QC executive vacancies, M.Pharm jobs in Andhra Pradesh, regulatory affairs careers, USFDA pharmaceutical openings, and pharmaceutical manufacturing jobs in India.

The company is inviting applications from qualified M.Sc, B.Pharm, and M.Pharm candidates with 2 to 8 years of experience in pharmaceutical quality systems, stability studies, IPQA, validation, market complaints, analytical testing, and QMS operations.

Professionals with experience in regulated manufacturing environments and strong pharmaceutical compliance exposure are encouraged to attend the walk-in interview.

Company Overview

APL HealthCare Limited is part of the globally recognized Aurobindo Pharma group, one of India’s leading pharmaceutical manufacturing organizations with a strong presence in domestic and international regulated markets.

The company operates advanced pharmaceutical manufacturing facilities focused on:

• Oral solid dosage manufacturing
• Pharmaceutical quality systems
• Regulated market operations
• API and formulation manufacturing
• Quality assurance compliance
• Analytical testing operations
• Validation and documentation systems

APL HealthCare facilities follow strict pharmaceutical manufacturing standards aligned with:

• cGMP regulations
• USFDA compliance
• International quality systems
• Data integrity requirements
• Validation protocols
• Pharmaceutical documentation standards

The pharmaceutical industry continues to invest heavily in quality operations because global regulatory agencies demand high standards for:

• Product quality
• Documentation compliance
• Manufacturing consistency
• Validation processes
• Batch traceability
• Stability monitoring
• Market complaint handling

Professionals working in QA and QC functions remain highly valuable in regulated pharmaceutical manufacturing industries.

Job Role & Responsibilities

Departments Hiring

• Quality Control (QC)
• Quality Assurance (QA)

Designation

• Executive
• Senior Executive

Experience Required

• 2 to 8 Years

Primary Keyword

Pharmaceutical QA QC Jobs

Quality Control Department Responsibilities

The Quality Control team will handle analytical and testing operations associated with pharmaceutical manufacturing.

QC Sections

• RM (Raw Material)
• IPFP
• Stability Studies

Key Responsibilities in QC

Selected candidates will perform:

• Raw material analysis
• In-process testing
• Finished product analysis
• Stability sample evaluation
• Instrument handling
• Laboratory documentation
• Data review and reporting
• Analytical compliance activities

Candidates should possess understanding of pharmaceutical analytical procedures and laboratory quality standards.

Stability Testing Activities

Professionals will support:

• Stability studies
• Stability chamber monitoring
• Analytical sample testing
• Product shelf-life evaluation
• Documentation maintenance

Stability operations are essential for regulated pharmaceutical product approvals.

Laboratory Documentation

The role requires strong knowledge of:

• Analytical records
• Laboratory notebooks
• SOP documentation
• Data integrity practices
• Audit readiness
• Compliance documentation

Candidates with experience in regulated pharmaceutical laboratories will have an added advantage.

Quality Assurance Department Responsibilities

The Quality Assurance team will oversee manufacturing quality systems and regulatory compliance activities.

QA Sections

• IPQA
• Validation
• QMS
• Market Complaints
• AQA

Key Responsibilities in QA

Selected professionals will manage:

• In-process quality assurance activities
• Batch record review
• Validation support
• SOP compliance monitoring
• Quality systems management
• Documentation review
• Manufacturing quality checks
• Compliance verification

IPQA Operations

Candidates will perform:

• Line clearance activities
• Process monitoring
• In-process checks
• Shop-floor QA support
• Documentation review
• Manufacturing compliance verification

Validation Activities

Professionals will support:

• Process validation
• Equipment qualification
• Cleaning validation
• Validation documentation
• Compliance reporting

QMS & Market Complaint Handling

Responsibilities may include:

• Quality Management System operations
• Deviation management
• CAPA implementation
• Market complaint investigation
• Compliance review
• Risk assessment activities

Regulatory Compliance

The company expects candidates to maintain compliance with:

• cGMP standards
• Regulatory guidelines
• Pharmaceutical quality systems
• Documentation protocols
• Audit requirements

Eligibility / Qualifications

Educational Qualification

Candidates with the following qualifications are eligible:

• M.Sc
• B.Pharm
• M.Pharm

Relevant Courses

Pharmaceutical Quality Assurance, Pharmaceutical Analysis, Pharmaceutics, Industrial Pharmacy, Analytical Chemistry, Microbiology, Quality Management Systems, Regulatory Affairs, Pharmaceutical Technology, Drug Regulatory Affairs, Biochemistry

Experience Requirement

• 2 to 8 years of pharmaceutical industry experience

Preferred Skills

Candidates with expertise in the following areas will be preferred:

• Pharmaceutical QA operations
• QC analytical testing
• Stability studies
• IPQA activities
• Validation documentation
• QMS systems
• Regulatory compliance
• Data integrity
• Laboratory documentation
• GMP compliance

Preferred Industry Exposure

Candidates with experience in:

• Regulated pharmaceutical plants
• USFDA-approved facilities
• Formulation manufacturing units
• Pharmaceutical analytical laboratories
• Compliance-focused environments

will receive preference during shortlisting.

Why QA & QC Careers Are Growing in the Pharma Industry

Quality Assurance and Quality Control remain among the highest-demand functions in pharmaceutical manufacturing because companies must maintain strict compliance with international regulatory standards.

The demand for experienced QA and QC professionals continues to rise due to:

• Expansion of regulated market manufacturing
• Increased global pharmaceutical exports
• Regulatory inspections
• Stability study requirements
• Validation operations
• Data integrity expectations
• Quality documentation controls

Professionals with QA/QC expertise can build strong long-term careers in:

• Pharmaceutical Manufacturing
• Compliance Management
• Regulatory Affairs
• Validation Operations
• Analytical Development
• Corporate Quality Assurance
• Quality Systems Management

Location & Salary

Work Location

APL HealthCare Limited – Unit IV Menakur SEZ, Naidupeta, Tirupati District, Andhra Pradesh – 524421

Naidupeta and the Tirupati pharmaceutical belt are emerging as important pharmaceutical manufacturing hubs offering strong career opportunities in:

• Formulation manufacturing
• API production
• QA/QC operations
• Regulatory manufacturing
• Pharmaceutical packaging
• Stability testing laboratories

Estimated Salary Range

Based on current pharmaceutical industry standards:

• Executive Level: ₹4.5 LPA to ₹7 LPA
• Senior Executive Level: ₹7 LPA to ₹10 LPA

Compensation may vary depending on:

• Years of experience
• QA/QC specialization
• Regulatory exposure
• Validation expertise
• Stability testing experience
• Current salary structure

Candidates with strong exposure to regulated pharmaceutical environments often receive premium compensation.

Application Process

Interested candidates can attend the walk-in interview directly at the interview venue.

Walk-In Interview Details

• Date: 23 May 2026
• Day: Saturday
• Time: 10:00 AM to 02:00 PM

Interview Venue

APL HealthCare Limited – Unit IV Menakur SEZ, Naidupeta, Tirupati District, Andhra Pradesh

Email Application

Candidates unable to attend the walk-in interview can send their resumes through email.

Email ID: praveenkumar.gullipalli@aurobindo.com

Documents to Carry

Applicants should carry:

• Updated Resume
• Educational Certificates
• Experience Certificates
• Salary Slips
• Government ID Proof
• Passport-size photographs

Important Recruitment Disclaimer

APL HealthCare Limited and Aurobindo group companies follow a strict merit-based recruitment process.

The company does not:

• Charge recruitment fees
• Accept security deposits
• Authorize agents for paid recruitment

Candidates are advised to avoid fraudulent job offers requesting money in exchange for employment opportunities.

Career Growth Opportunities in Pharmaceutical QA & QC

Professionals joining pharmaceutical QA and QC departments can build long-term careers in:

• Regulatory Affairs
• Corporate QA
• Quality Systems
• Validation Management
• Analytical Development
• Compliance Audits
• Manufacturing Quality Operations
• Stability Management

With experience, professionals can progress into:

• QA Manager
• QC Manager
• Validation Lead
• Compliance Head
• Plant Quality Head
• Regulatory Affairs Specialist

FAQs

1. Which company is conducting this walk-in drive?

APL HealthCare Limited, part of the Aurobindo group, is conducting the walk-in interview.

2. Which departments are hiring?

The company is hiring for Quality Assurance and Quality Control departments.

3. What qualifications are eligible?

Candidates with M.Sc, B.Pharm, and M.Pharm qualifications can apply.

4. What experience is required?

Candidates with 2 to 8 years of pharmaceutical industry experience are eligible.

5. What is the work location?

The work location is Naidupeta, Tirupati District, Andhra Pradesh.

6. How can candidates apply?

Candidates can attend the walk-in interview or send resumes to praveenkumar.gullipalli@aurobindo.com.

Summary Table

Company	APL HealthCare Limited (Aurobindo Group)
Department Vacancies	Quality Assurance, Quality Control
Qualification	M.Sc, B.Pharm, M.Pharm
Experience	2–8 Years
Location	Naidupeta, Tirupati District, Andhra Pradesh