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
Aurobindo 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 / MSc. (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
You must sign in to apply for this position.