Aurobindo Pharma Hiring for Quality Control Role
- About Aurobindo Pharma
- Current Openings – Quality Control (QC)
- Department: Quality Control
- Sections: FP (Finished Products), IP (In-Process), GLP, RM (Raw Materials)
- Job Designation: Executive / Sr. Executive
- Experience Required: 2 to 8 Years
- Work Location:
- Key Responsibilities
- Eligibility Criteria
- Application Process
If you’re an experienced pharma professional aiming to make a meaningful impact in quality control, here’s your chance! Aurobindo Pharma, a globally recognized pharmaceutical company, is currently hiring for Executive and Senior Executive positions in the Quality Control department at APL Health Care Limited – Unit IV, located in Naidupeta, Tirupati District, Andhra Pradesh.
This opportunity is ideal for individuals with strong analytical skills and experience in Finished Products (FP), In-Process (IP), Good Laboratory Practices (GLP), or Raw Material (RM) testing.
About Aurobindo Pharma
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📱 Join Click HereAurobindo Pharma Limited is a renowned name in the global pharmaceutical industry, consistently recognized for its commitment to affordable and accessible healthcare. Headquartered in Hyderabad, Aurobindo manufactures a wide range of generic pharmaceuticals and active pharmaceutical ingredients (APIs) with a presence in over 150 countries.
Joining Aurobindo means being a part of a forward-thinking company with a clear focus on quality, innovation, and global reach.
Current Openings – Quality Control (QC)
Department: Quality Control
Sections: FP (Finished Products), IP (In-Process), GLP, RM (Raw Materials)
Job Designation: Executive / Sr. Executive
Experience Required: 2 to 8 Years
Work Location:
APL Health Care Limited, Unit IV
SEZ Menakur, Naidupeta,
Tirupati District, Andhra Pradesh – 524421
Key Responsibilities
Conduct quality analysis of FP, IP, GLP, and RM samples in compliance with cGMP standards.
Perform routine chemical and instrumental testing (HPLC, GC, UV, IR, etc.).
Ensure timely documentation and reporting of test results.
Collaborate with cross-functional teams to resolve quality issues.
Support audits and regulatory inspections as per USFDA, MHRA, and WHO-GMP requirements.
Eligibility Criteria
Educational Qualification:
B. Pharm / M. Pharm / M.Sc. (Chemistry or relevant specialization)
Experience:
2 to 8 years of experience in pharmaceutical QC functions, preferably in a regulated manufacturing environment.
Key Skills:
Proficiency in analytical techniques (HPLC, GC, UV, etc.)
Good documentation practices
Strong understanding of regulatory compliance
Team collaboration and time management
Application Process
Interested candidates are encouraged to share their updated CVs via email to:
📧 naidupetahr@aurobindo.com
📞 Contact Person: Zuha (HR) – 9581444337
