[Freshers & Experienced] Aurobindo Pharma Hiring for QA / QC / Engineering
Aurobindo Pharma Limited (APL) is a dynamic and rapidly growing Indian multinational pharmaceutical manufacturing company, with an impressive turnover exceeding US$2.8 billion for the fiscal year 2018-19. Our extensive global presence spans more than 34 countries, with products exported to 155 nations worldwide. As the second-largest generic pharmaceutical company in the United States, based on prescriptions dispensed, APL is a formidable force in the industry. Additionally, we are proud to be among the top 10 generic players in key European markets, including France, Germany, Portugal, the UK, Italy, the Czech Republic, the Netherlands, and Belgium.
We are excited to announce that our Jadcherla Hyderabad Unit is currently seeking talented and motivated professionals to join our team. If you are passionate about making a meaningful impact in the pharmaceutical industry and are looking to advance your career, we invite you to explore the following opportunities:
1. Department: QA-IT
- Qualification: IT, BCA, MCA, B.Tech
- Experience: 0-4 years
- Job Description: In this role, you will be responsible for Document Management Systems (DMS), ensuring compliance with GXP standards, upgrading software systems, and working as a front-end developer. This is an excellent opportunity for individuals with a background in IT who are eager to contribute to quality assurance through technology.
2. Department: QA Validation (Cleaning Validation)
- Qualification: M.Pharm, B.Pharm
- Experience: 7-9 years
- Job Description: We are looking for professionals with hands-on experience in cleaning validation and equipment qualification. Exposure to a USFDA-approved Oral Solid Dosage (OSD) plant is essential. This role is crucial for ensuring that our manufacturing processes meet the highest standards of cleanliness and safety, in compliance with global regulatory requirements.
3. Department: Quality Control (QC)
- Qualification: B.Sc, M.Sc
- Experience: 8-10 years
- Job Description: As a Quality Control investigator, you will play a key role in managing Out of Specification (OOS) and Out of Trend (OOT) results, handling Quality Management Systems (QMS), and working with Empower 3 software. The ideal candidate should have experience in OSD formulation units within USFDA-approved plants, without prior exposure to API plants. This role offers a challenging environment where your expertise will directly contribute to maintaining the highest quality standards in our products.
4. Department: Engineering
- Qualification: Instrumentation, B.Tech, M.Tech
- Experience: 6-9 years
- Job Description: This role involves the upgradation of machinery and PLC systems, process maintenance, and preventive maintenance planning. The successful candidate will have experience handling compression, granulation, and packing machinery, particularly those compliant with 21 CFR regulations. Prior experience in a USFDA-approved OSD plant is required, and we are looking for multi-talented individuals who can manage complex engineering tasks with precision.
Why Join Us?
At Aurobindo Pharma, you will be part of a company that is not only the 3rd largest pharmaceutical company globally but also one that operates a SA8000 compliant plant. This means we are committed to maintaining the highest standards of social accountability, ensuring fair treatment of workers, and providing a safe and healthy working environment. We offer the best of benefits to our employees, recognizing their contributions to our continued success.
How to Apply:
If you are interested in joining our team and contributing to a company that is at the forefront of the pharmaceutical industry, we encourage you to share your resume with us. Please send your resume to [email protected].
This is your chance to be part of a leading pharmaceutical company that is making a significant impact on global health. We look forward to receiving your application and potentially welcoming you to the Aurobindo Pharma family!
