Medopharm is a leading pharmaceutical company committed to delivering high-quality healthcare solutions across global markets. We focus on innovation, compliance, and excellence in manufacturing and marketing.
We are looking for dynamic professionals to join our growing team:
🔹 Regulatory Affairs – 5–10 yrs (Regulated Market)
Role: Author CMC sections, handle eCTD submissions, manage queries from global regulatory authorities (UK, EU, Australia), and oversee lifecycle & change control.
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