Manager- Drug Regulatory Affairs

Venus Remedies -
Panchkula, Haryana

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Job details

Full-time

Qualifications

B.Pharma
Research
Bachelor's degree
M.Pharma

Full job description

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, New drugs/New 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

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