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If you’re passionate about building a career in Regulatory Affairs within the pharmaceutical industry, Eurolife Healthcare Pvt. Ltd. offers a golden opportunity. Based in Roorkee, Uttarakhand, this full-time role is ideal for freshers and graduates (including M.Pharm) eager to gain real-world experience in regulatory documentation, dossier preparation, and product registration.
Join one of India’s trusted healthcare companies and contribute to ensuring product compliance and regulatory excellence.
Key Responsibilities
As a Regulatory Affairs Associate, you will:
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- Assist in preparing and compiling regulatory submissions such as product registration dossiers, renewals, and variations.
- Coordinate with QA, QC, Production, and R&D teams to collect technical data for filings.
- Maintain and update regulatory databases and document control systems.
- Review product labeling, artwork, and promotional materials for compliance.
- Stay updated with current CDSCO, FDA, EMA, and WHO guidelines.
- Support in addressing regulatory queries or deficiencies raised by authorities.
- Maintain organized and auditable regulatory files and archives.
Eligibility & Qualifications
- Experience: 0–2 years
- Qualification: Graduate / M.Pharm (freshers eligible)
- Location: Roorkee, Uttarakhand
- Salary: ₹25,000 per month (in-hand)
Why Join Eurolife Healthcare?
- Hands-on experience in Regulatory Affairs within a reputed pharma company
- Exposure to global regulatory frameworks (CDSCO, WHO, FDA, EMA)
- Collaborative, learning-driven environment
- Competitive entry-level salary package
How to Apply
Interested candidates can email their updated CV directly to:
📧 harishkumar@eurolifehealthcare.com
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