About Aurobindo Pharma Limited:
Aurobindo Pharma Limited is an Indian pharmaceutical manufacturing company headquartered in HITEC City, Hyderabad, India. The company manufactures generic pharmaceuticals and active pharmaceutical ingredients. The company’s area of activity includes six major therapeutic/product areas: antibiotics, antiretrovirals, cardiovascular products, central nervous system products, gastroenterological, and anti-allergics. The company markets these products in over 125 countries Its marketing partners include AstraZeneca and Pfizer.
Aurobindo Pharma plans to expand its product portfolio with high-value products in oncology, hormones, biosimilars, and novel drug delivery solutions like depot injections, inhalers, patches, and films. It has also set its sights on geographic expansion in new territories like Poland, Italy, Spain, the Czech Republic, Portugal, and France, as the generic drug market in these countries is relatively small.
In 2017, Aurobindo Pharma inked a pact to acquire Portugal’s Generis Farmaceutica SA from Magnum Capital Partners for a consideration of €135 million. It also acquired four biosimilar products from Swiss firm TL Biopharmaceutical AG.
Aurobindo Pharma Ltd. signed a definitive agreement to purchase the Apotex businesses in Poland, the Czech Republic, the Netherlands, Spain, and Belgium. The agreement is conditional on the receipt of competition clearances for the transaction by the Dutch and Polish authorities. As part of the proposed sale, Apotex will enter into a transitional manufacturing and supply arrangement with Aurobindo to support the ongoing growth plans of these businesses.
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About Aurobindo Pharma Limited Job Vacancy:
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🌍 We’re Hiring – Regulatory Affairs Professionals (Formulation R&D) | EU Markets 🚀
An exciting opportunity awaits you at Aurobindo Pharma! We are on the lookout for passionate Regulatory Affairs professionals to join our Formulation R&D team supporting EU markets.
If you hold an M.Pharm in Pharmaceutics/Pharmaceutical Analysis and bring 8–10 years of relevant experience in oral solid and liquid dosage submissions, this role could be your next big leap!
📩 Please share your resume at Pooja.Uppalapati@aurobindo.com or hrrc1@aurobindo.com with the subject line: “Application for EU Market”
🔄 Referrals are welcome too!
📋 Job Details Table
| Category | Details |
|---|---|
| Position | Regulatory Affairs Professional – Formulation R&D (EU Markets) |
| Department | Regulatory Affairs – Research & Development |
| Qualification | M. Pharm in Pharmaceutics / Pharmaceutical Analysis |
| Experience | 8–10 years in Regulatory Affairs (Formulation, Oral Solid Dosage) |
| Job Location | Hyderabad |
| Openings | EU Market – Hands-on experience required |
| Key Responsibilities | 1. Post-approval lifecycle management for oral solid & liquid dosage in EU2. Maintenance of status: Customer status, DCP-MRP & Renewal timetables, Variations, Batch sizes, shelf life, CEP & Audit status3. Compilation of updated dossier & responding to agency comments (MRP/DCP/National) |
| Required Skills | Regulatory submission handling, EU regulatory frameworks, dossier compilation, agency communication |
| Contact Details | Email: Pooja.Uppalapati@aurobindo.com / hrrc1@aurobindo.comSubject: “Application for EU market” |
