Aurobindo Pharma Ltd (APL) is a leading multinational pharmaceutical company with a global presence and a strong commitment to innovation. With over US$2.8 billion in revenue (2018-19 figures), APL is a prominent player in the global pharmaceutical market, exporting products to 155 countries and holding a significant position in numerous key markets. Notably, APL ranks as the second largest generic pharmaceutical company in the USA based on prescriptions dispensed and is among the top 10 generic players in France, Germany, Portugal, the UK, Italy, the Czech Republic, the Netherlands, and Belgium. This rapid growth and global reach create exciting opportunities for talented professionals seeking rewarding careers.
Current Job Openings at Aurobindo Pharma
Aurobindo Pharma currently has several key openings within its Regulatory Affairs and Research & Development departments, offering excellent career progression opportunities for experienced and skilled professionals. Below are details of the current vacancies:
1. Regulatory Affairs Specialist (EU Regulatory Team, OSD)
- Position: Regulatory Affairs Specialist
- Team: EU Regulatory team (Oral Solid Dosage forms – OSD)
- Experience: 2 to 10 years of experience in regulatory affairs within the pharmaceutical industry.
- Qualification: M.Pharmacy is required.
- Responsibilities: This role will involve a broad range of responsibilities encompassing regulatory submissions, compliance, and lifecycle management for OSD products within the European Union. Strong knowledge of EU regulatory guidelines and procedures is essential.
2. Regulatory Affairs Specialist (US & Canada Team, Injectable)
- Position: Regulatory Affairs Specialist
- Team: US & Canada Regulatory team (Injectable products)
- Experience: 2 to 10 years of experience in regulatory affairs within the pharmaceutical industry, with a focus on injectable products.
- Qualification: M.Pharmacy is required.
- Responsibilities: The successful candidate will be responsible for regulatory submissions, compliance, and lifecycle management for injectable products within the US and Canadian markets. Expertise in US FDA regulations and Canadian regulatory requirements is crucial.
3. Research & Development (R&D) – Cost Improvement Projects (OSD)
- Position: R&D Specialist – Cost Improvement Projects
- Area: Oral Solid Dosage forms (OSD)
- Experience: 2 to 6 years of experience in pharmaceutical R&D with a focus on cost optimization and process improvements within OSD manufacturing.
- Qualification: M.Pharmacy is required.
- Responsibilities: This position requires a strong understanding of pharmaceutical manufacturing processes and a proven ability to identify and implement cost-saving initiatives while maintaining high quality standards.
4. Regulatory Affairs Document Controller – CMC-SPD (Reviewer)
- Position: Regulatory Affairs Document Controller – CMC-SPD (Reviewer)
- Experience: 2 to 6 years of experience in US regulatory affairs, with a focus on CMC (Chemistry, Manufacturing, and Controls) and SPD (Stability and Product Development) documentation.
- Qualification: M.Pharmacy or B.Pharmacy.
- Responsibilities: This role involves reviewing and managing CMC and SPD documentation for regulatory submissions. A strong understanding of US FDA guidelines and excellent attention to detail are essential.
Why Choose a Career at Aurobindo Pharma?
Aurobindo Pharma offers a dynamic and challenging work environment with opportunities for professional growth and development. We are committed to fostering a culture of innovation and collaboration, providing our employees with the tools and resources they need to succeed. As a global leader in the pharmaceutical industry, we offer competitive compensation and benefits packages.
How to Apply
Interested and qualified candidates are encouraged to apply by sending their resume to the following WhatsApp number: +91 8328053327 (Please note country code added for clarity).
