Exciting Career Opportunities at Aurobindo Pharma Limited – Jadcherla Unit
Aurobindo Pharma Limited (APL), a growing Indian multinational pharmaceutical manufacturing firm, is looking for experienced professionals to join its Jadcherla Unit. With a strong global presence, APL offers incredible opportunities for those with expertise in Quality Control and Quality Assurance in a USFDA-approved OSD (Oral Solid Dosage) formulation environment.
Key Points:
- Company: Aurobindo Pharma Ltd.
- Location: Jadcherla Unit
- Roles Available: Quality Control (Chromatography), Quality Control (Investigator), Quality Assurance (Investigator, Documentation/QMS, BMR/BPR Issuance)
- Experience Required: 3 to 14 years, depending on the role.
- Industry: USFDA-approved OSD formulation only (API and Sterile formulation experience not considered)
- How to Apply: Interested candidates can send their resume to Manjesh.anantramnayak@aurobindo.com
About Aurobindo Pharma Limited (APL)
Aurobindo Pharma Limited is a global leader in the pharmaceutical industry with revenues exceeding $2.8 billion for the 2018-19 fiscal year. With a strong foothold in more than 34 countries and exports to 155 nations, APL is renowned for its commitment to quality and innovation. It is the second-largest generic pharmaceutical company in the USA and a top player across Europe, including France, Germany, the UK, and the Netherlands. APL manufactured over 33 billion diverse dosage forms in 2018-19, making it a key player in the pharmaceutical industry worldwide.
APL operates with a network of 27 manufacturing facilities and five R&D centers, ensuring continuous growth and innovation. Now, they are looking for professionals to fill multiple roles in their Jadcherla Unit.
Open Positions at APL Jadcherla Unit
Quality Control – Chromatography
Experience: 3 to 7 Years
If you have expertise in High-Performance Liquid Chromatography (HPLC) software such as Empower 3, and exposure to LCMS (Liquid Chromatography-Mass Spectrometry), this is the perfect opportunity for you. This role involves working with in-process, finished, and stability sections, ensuring that quality standards are met across various phases of product testing.
Quality Control – Investigator
Experience: 10 to 14 Years
This position calls for candidates with in-depth experience in handling QMS (Quality Management System) investigations related to OOS (Out of Specification) and OOT (Out of Trend) issues. You will be responsible for identifying root causes, providing corrective actions, and ensuring compliance with industry regulations.
Quality Assurance – Investigator
Experience: 7 to 9 Years
In this role, you will be managing QMS, production, and QA-related investigations. The job requires hands-on experience handling OOS and OOT investigations and interacting with USFDA auditors. Strong skills in root cause analysis and various investigation tools are critical for success in this position.
Quality Assurance – Documentation/QMS
Experience: 4 to 7 Years
This role involves managing APQR (Annual Product Quality Review) and QMS documentation. Candidates should have hands-on experience with managing deviations, CAPA (Corrective and Preventive Actions), and other essential documentation processes that ensure regulatory compliance.
Quality Assurance – BMR and BPR Issuance
Experience: 4 to 6 Years
If you have experience in issuing Batch Manufacturing Records (BMR) and Batch Packing Records (BPR), along with batch card preparation, this role offers a great opportunity to contribute to maintaining the highest quality standards in pharmaceutical production.
Why Join Aurobindo Pharma Limited?
Joining Aurobindo Pharma means being part of a global leader in the pharmaceutical sector. The company’s commitment to high-quality standards, innovation, and patient care makes it a rewarding place to build a career. As a member of the APL team, you will have the chance to contribute to life-changing medicines while growing your own professional skills in a dynamic, supportive environment.
How to Apply
If you meet the experience requirements and have worked in USFDA-approved OSD formulation, Aurobindo Pharma Ltd. invites you to apply. Please note that experience in API (Active Pharmaceutical Ingredients) and sterile formulation will not be considered. Interested candidates should send their resume to Manjesh.anantramnayak@aurobindo.com.
Take the next step in your pharmaceutical career by joining a leader in the global market. Apply today and become a part of Aurobindo Pharma’s journey to excellence!
