Aurobindo Pharma Ltd. (APL), a leading multinational pharmaceutical company, is currently seeking talented and experienced professionals to join its 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 major player in the generic pharmaceutical industry. Ranked as the second largest generic company by Rx dispensed in the USA, and among the top 10 generic players in several key European markets including France, Germany, Portugal, UK, Italy, Czech Republic, Netherlands, and Belgium, APL offers a dynamic and rewarding work environment.
Exciting Career Opportunities at a Global Pharmaceutical Leader
Aurobindo Pharma is committed to providing high-quality, affordable medications worldwide. Our success is driven by our dedicated employees, and we are actively seeking individuals with a passion for pharmaceutical innovation and a commitment to excellence. We currently have several exciting openings for experienced professionals in the following areas:
1. Regulatory Affairs (RA) – EU Regulatory Team (OSD)
Job Description: This role within our EU Regulatory Team focuses on Oral Solid Dosage (OSD) products. You will be responsible for various regulatory activities, including but not limited to, submissions, registrations, and maintenance of marketing authorizations for our products within the European Union. Strong knowledge of EU regulatory guidelines and experience in the pharmaceutical industry is essential.
Experience: 2-10 years in Regulatory Affairs
Qualifications: M.Pharmacy required.
2. Regulatory Affairs (RA) – US & Canada Team (Injectable)
Job Description: Join our North American Regulatory Affairs team, specializing in Injectable products. You will play a crucial role in ensuring regulatory compliance for our injectable portfolio in the US and Canadian markets. This involves strategic planning, execution, and management of regulatory submissions and related documentation. Strong communication and teamwork skills are vital.
Experience: 2-10 years in Regulatory Affairs, specifically in injectables.
Qualifications: M.Pharmacy required.
3. Formulation Research & Development (FR&D) – OSD Cost Improvement Projects
Job Description: We are seeking a highly motivated and results-oriented professional to join our Formulation Research & Development team. Your focus will be on identifying and implementing cost-saving initiatives for our Oral Solid Dosage (OSD) products. This role requires a deep understanding of pharmaceutical manufacturing processes and cost optimization strategies.
Experience: 2-6 years in Formulation Research & Development within the pharmaceutical industry.
Qualifications: M.Pharmacy required.
4. Regulatory Affairs and Documentation (RAD) CMC-SPD (Reviewer) – US Regulatory Affairs
Job Description: This crucial role involves reviewing Chemistry, Manufacturing, and Controls (CMC) documentation for submissions to the US regulatory authorities. The ideal candidate will possess strong analytical skills and a thorough understanding of cGMP and US FDA regulations. Experience in the review and assessment of CMC data packages is essential.
Experience: 2-6 years in US Regulatory Affairs, with a focus on CMC documentation.
Qualifications: M.Pharmacy or B.Pharmacy.
How to Apply
Are you ready to embark on a challenging and rewarding career journey with a global pharmaceutical leader? If you possess the necessary qualifications and experience, and are eager to contribute to our mission of delivering high-quality medications, we encourage you to apply.
To express your interest, please send your resume via WhatsApp to: +91-8328053327
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Note: Please ensure your resume is up-to-date and clearly highlights your relevant experience and qualifications. We look forward to hearing from you!
