Preparation, Review and successful submissions of CTD/e-CTD format Dossiers Module I to V of New Fixed Dose Combination dossiers in EU, USFDA, Canada, South Africa, and other regulated markets etc. as per country specific procedures & requirements.

Job Posting: 09/24/2025

Panchkula

JOB REQUIREMENTS

- Mandatory Qualifications

M.Pharma

Encouraged Qualifications

B.Pharma

- Work Experience in Relevant Field

7-12 Years

Technical Skills Required

Should have minimum seven-eight years experience in core Regulatory Affairs function with atleast three-four years RA experience in areas like, Parentral dosage forms, Recent drugs/Recent FDCs/Research products handling experience

JOB DESCRIPTION

- Who You'll Work With





Working under the direct guidance of the HOD in executing the Company Regulatory Strategy effectively & timely to meet Company Business goals and adherence to high Quality and Regulatory standards in dossiers for all the Research products.

- Soft Skills Required

Good interpretation & applicability skills for ICH Q/S/E, EU.Must have a proven ability to communicate effectively in both written and verbal format

Must have experience of ROW/ASIAN Market

- Functional Area

Research and Development

- Recruitment Status

Open

- Employment Type

Full Time

- Date of Joining

Immediate

📌 Manager- Drug Regulatory Affairs (India)
🏢 Venus Remedies
📍 India