Join Aurobindo Pharma: Exciting Opportunities in Quality, Assurance, and Production
Summary:
Aurobindo Pharma Limited, a leading global pharmaceutical company, is seeking experienced and motivated professionals to join our state-of-the-art Unit-XII facility in Bachupally, Hyderabad. We have immediate openings in Quality Control, Quality Assurance, and Production (Packing and Injectables) for roles ranging from Executive to Deputy Manager. If you possess a strong background in pharmaceutical formulation and are driven to contribute to a dynamic and growing organization, we encourage you to apply.
About Aurobindo Pharma:
Aurobindo Pharma Limited is a renowned name in the pharmaceutical industry, recognized for our commitment to quality, innovation, and global reach. As one of India’s leading generic pharmaceutical companies and a major player in the US market, we export our products to over 155 countries. We are dedicated to fostering a collaborative and rewarding work environment where talented individuals can thrive and contribute to our mission of providing accessible and affordable healthcare solutions worldwide.
Open Positions:
We are currently hiring for the following positions at our Unit-XII facility in Bachupally, Hyderabad:
- Department: Quality Control (QC)
- Department: Quality Assurance (QA)
- Department: Production – Packing (Oral Solids)
- Department: Production – Injectable (Sterile)
Available Roles:
- Executive
- Senior Executive
- Deputy Manager
Responsibilities:
The specific responsibilities will vary depending on the department and role, but generally include:
Quality Control (QC):
- Performing analytical testing of raw materials, in-process samples, and finished products.
- Conducting stability studies and ensuring adherence to stability protocols.
- Maintaining accurate and complete documentation of all testing activities.
- Operating and maintaining laboratory equipment.
- Analyzing data and identifying trends to ensure product quality.
Quality Assurance (QA):
- Handling IPQA (In-Process Quality Assurance) activities to monitor manufacturing processes.
- Managing QMS (Quality Management System) documentation and implementation.
- Participating in validation activities, including equipment, process, and cleaning validation.
- Preparing for and participating in regulatory audits (USFDA, EU, MHRA, etc.).
- Reviewing and approving batch records, SOPs, and other quality-related documents.
Production – Packing (Oral Solids):
- Managing packing lines for blister and bottle packing of oral solid dosage forms.
- Ensuring efficient and compliant packing operations.
- Troubleshooting and resolving issues related to packing equipment and processes.
- Supervising and training packing line personnel.
- Maintaining accurate records of packing activities.
Production – Injectable (Sterile):
- Managing sterile injectable manufacturing processes for vials, ampoules, and pre-filled syringes (PFS).
- Ensuring aseptic processing techniques and adherence to strict sterile manufacturing guidelines.
- Overseeing equipment operation and maintenance in the injectable manufacturing area.
- Troubleshooting and resolving issues related to injectable manufacturing processes.
- Supervising and training injectable manufacturing personnel.
General Responsibilities (All Departments):
- Ensuring compliance with cGMP (current Good Manufacturing Practices), ICH (International Council for Harmonisation) guidelines, and global regulatory standards.
- Leading investigations into deviations, out-of-specification (OOS) results, and other quality-related issues.
- Implementing CAPA (Corrective and Preventive Action) plans to address identified issues.
- Participating in continuous improvement initiatives to enhance quality and efficiency.
Qualifications and Skills:
- B.Pharmacy or M.Sc in Microbiology/Biotechnology from a recognized university.
- Experience:
- Executive & Senior Executive: 2–6 years of relevant formulation experience.
- Deputy Manager: 10–14 years of relevant formulation experience.
- Hands-on experience in pharmaceutical formulation, preferably in regulated markets (USFDA, EU, MHRA, etc.).
- Strong knowledge of GLP (Good Laboratory Practices), GMP, data integrity principles, and 21 CFR Part 11.
- Excellent documentation and communication skills.
- For Production roles, experience in injectables (aseptic processing) is highly desirable.
- Flexibility to work in rotational shifts.
- Immediate joiners are preferred.
Why Join Aurobindo Pharma?
- Growth Opportunity: Work in a fast-growing multinational pharmaceutical company with significant market presence.
- Global Exposure: Gain experience with USFDA, EU, and other major regulatory audits.
- Competitive Compensation: Receive an attractive salary, performance incentives, and opportunities for career progression.
- Advanced Facilities: Work in a modern facility equipped with advanced technology for both injectables and oral solids manufacturing.
- Employee Benefits: Enjoy comprehensive benefits including medical insurance, transport, and canteen facilities.
How to Apply:
Interested and qualified candidates are encouraged to submit their updated resume to:
Email: [email protected]
Subject Line: Application for [Department] – [Position] – Unit XII
(Please replace [Department] and [Position] with the specific department and role you are applying for.)
We are looking forward to receiving your application!