Apitoria Pharma Private Limited, a 100% subsidiary of Aurobindo Pharma Limited, is seeking talented Microbiology professionals for its Quality Control (QC) department in the API Division. This is an excellent opportunity for freshers and experienced candidates to join a leading pharmaceutical company.
Key Responsibilities:
- Perform microbiological testing of raw materials, in-process samples, and finished products.
- Conduct environmental monitoring (EM) in manufacturing areas.
- Perform sterility testing, microbial limit tests (MLT), endotoxin testing (LAL), and water analysis.
- Ensure compliance with GMP, GLP, and regulatory guidelines (USFDA, WHO, EU).
- Maintain documentation and assist in method validation & equipment calibration.
- Work in rotational shifts (including night shifts) as per manufacturing requirements.
Desired Skills:
- Strong knowledge of microbiological techniques & instrumentation.
- Familiarity with aseptic practices, media preparation, and microbial identification.
- Good documentation and data integrity practices.
- Ability to work in a fast-paced manufacturing environment.
About Apitoria Pharma (Aurobindo Pharma Subsidiary)
Apitoria Pharma Private Limited is a wholly-owned subsidiary of Aurobindo Pharma Limited, a globally recognized pharmaceutical company. Aurobindo Pharma is known for its high-quality APIs (Active Pharmaceutical Ingredients) and formulations, catering to regulated markets like the US, Europe, and emerging markets.
As part of the Aurobindo Group, Apitoria Pharma maintains high standards in manufacturing and quality control, ensuring compliance with international regulatory norms.
Why Join Apitoria Pharma?
✅ Career Growth in a reputed pharmaceutical company
✅ Learning Opportunities in GMP & regulatory compliance
✅ Stable Work Environment with industry-best practices
✅ Competitive Salary & Benefits
How to Apply?
Interested candidates can send their resumes to:
Email: raghavendra.kotnana@apitoria.com
Note: Preference will be given to male candidates due to rotational shift requirements in the manufacturing facility.
