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Rusan Pharma – Regulatory Affairs Officers & Executives job opening

Rusan Pharma Ltd Regulatory Affairs: Officer/ Executive Role


About the rusan pharma company; Rusan Pharma is a pharmaceutical company based in India. It was founded in 1994 and has since become a leading manufacturer and supplier of a wide range of generic and branded drugs. The company’s product portfolio includes products in the areas of anti-infectives, gastroenterology, cardiology, diabetology, pediatrics, and more. Rusan Pharma has a strong focus on research and development and has a number of research and development centers located throughout India. The company is committed to meeting the needs of patients and healthcare providers around the world and has a strong commitment to ethical business practices.

The company has a manufacturing facility in Kandivali, a suburb of Mumbai in the state of Maharashtra. The Kandivali facility is equipped with state-of-the-art machinery and technology and is capable of producing a wide range of pharmaceutical products. The facility is cGMP compliant and has been approved by various regulatory agencies, including the US FDA and the UK MHRA.

Rusan Pharma job openings information;

Rusan Pharma Ltd hiring for Officer / Executive – Regulatory Affairs (Formulation) department for ROW market at Kandivali (W), Mumbai.

Department: Regulatory Affairs

Job Description :
Rusan Pharma is pleased to announce multiple job opening in our Regulatory Affairs department for Regulated and Semi regulated market to be based at our corporate office Kandivali, Mumbai.

Job Summary: Regulatory Affairs Executive will be responsible for Dossier preparation and submissions for the below countries.

Market :

1) Australia and New Zealand.

2) Canada

3) Brazil and Mexico

4) CIS Countries

Job Profile / Desired Candidate Profile :

Experience: Candidate must have minimum of 01 – 6 years of experience in dossier preparation and submission in any of the above countries.

Should be well-versed with regulatory guidelines country-specific and ICH.

Must have experience in CTD/eCTD dossier preparation and submission.
Will be responsible for replying to queries raised by MOH.

Candidate should be well versed in Microsoft, Excel, and PowerPoint presentations.

Excellent written and verbal communication skills.

Application Process; Candidates with relevant experience please share your resume through email at and

%titl rusan pharma regulatory affairs officers executives job opening

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