Aurobindo Pharma Ltd., a leading Indian multinational pharmaceutical company, is seeking highly motivated and experienced professionals to join our growing team. With over US$2.8 billion in revenue (2018-19) and a global presence spanning more than 155 countries, Aurobindo Pharma is a dynamic and rapidly expanding force in the pharmaceutical industry. We are ranked as the 2nd largest generic company by Rx dispensed in the USA and among the top 10 generic players in key European markets including France, Germany, Portugal, the UK, Italy, Czech Republic, Netherlands, and Belgium. This is an exceptional opportunity to build your career with a global leader.
Current Openings at Aurobindo Pharma Ltd.
We are currently recruiting for several key positions within our Regulatory Affairs and Research & Development departments. These roles offer excellent growth potential and the chance to contribute to the development and delivery of vital medications worldwide.
1. Regulatory Affairs Associate (RA) – EU Regulatory Team (OSD)
- Experience: 2 to 10 years
- Qualification: M.Pharmacy (Master of Pharmacy) required
- Responsibilities: This role will involve a variety of tasks related to the regulatory submission and approval of oral solid dosage (OSD) pharmaceutical products within the European Union. Specific responsibilities may include compiling regulatory documents, interacting with regulatory agencies, and ensuring compliance with EU regulations.
2. Regulatory Affairs Associate (RA) – US & Canada Team (Injectable)
- Experience: 2 to 10 years
- Qualification: M.Pharmacy (Master of Pharmacy) required
- Responsibilities: This position focuses on the regulatory submission and approval process for injectable pharmaceutical products in the US and Canada. You will be involved in all aspects of the regulatory lifecycle, from initial application to post-market surveillance. Experience with US FDA regulations is essential.
3. Formulation Research & Development (F&R&D) – OSD Cost Improvement Projects
- Experience: 2 to 6 years
- Qualification: M.Pharmacy (Master of Pharmacy) required
- Responsibilities: This role involves contributing to cost reduction initiatives for oral solid dosage (OSD) formulations. You will work collaboratively with a team of scientists and engineers to identify and implement cost-saving measures without compromising product quality or efficacy.
4. Regulatory Affairs and Documentation CMC-SPD (Reviewer)
- Experience: 2 to 6 years (US Regulatory Affairs experience preferred)
- Qualification: M.Pharmacy or B.Pharmacy (Bachelor of Pharmacy)
- Responsibilities: This position involves reviewing Chemistry, Manufacturing, and Controls (CMC) documentation and Standard Procedures Documents (SPD) to ensure compliance with US regulatory guidelines. You will play a critical role in maintaining regulatory compliance for our products.
Key Skills and Attributes We Seek:
Across all positions, we are looking for candidates who possess:
- Strong analytical and problem-solving skills: The ability to analyze complex data and identify solutions is critical.
- Excellent communication skills: Effective communication with internal and external stakeholders is crucial.
- Teamwork and collaboration: These positions require close collaboration with other team members.
- Proficiency in relevant software: Experience with regulatory submission software and other relevant applications is a plus.
- Detail-oriented approach: Accuracy and attention to detail are essential for regulatory compliance.
How to Apply:
Interested and qualified candidates are encouraged to apply by submitting their resume via WhatsApp to: +91 8328053327. Please ensure your resume clearly highlights your relevant experience and qualifications.
We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.
