Regulatory Affairs Officer (Pharm‑D)

About the role

We are looking for a Regulatory Affairs Officer with a Pharm‑D background to join our team in Johar Town, Lahore. You will play a key role in ensuring regulatory compliance and successful product registrations for pharmaceuticals and nutraceuticals.

Key responsibilities

• Prepare, compile, and submit dossiers to DRAP.
• Ensure all submissions comply with regulatory requirements.
• Respond to DRAP queries and maintain accurate documentation.

Required profile

• Pharm‑D degree.
• 1–3 years of experience in regulatory affairs or dossier preparation.
• Strong attention to detail and excellent documentation skills.

Required skills

• Hands‑on experience with CTD/ACTD dossier compilation for pharmaceuticals and nutraceuticals.
• In‑depth knowledge of DRAP regulations and submission processes.
• Familiarity with CMC documentation, stability data, labeling, and GMP requirements.
• Proficiency in MS Word and MS Excel.