Crius Life Sciences is a leading Nutraceutical Specialties Manufacturer specializing in Private Label and Contract Manufacturing. The company is renowned for its expertise in producing:
- Vegetarian Softgel Capsules
- Effervescent Tablets
- Bi-Layered Sustained-Release Tablets
Certifications: US FDA, WHO, HACCP, ISO 22000
Global Reach: Exports to multiple countries worldwide.
Job Description: DRA Executive
The DRA (Drug Regulatory Affairs) Executive will handle regulatory compliance, documentation, and liaise with authorities to ensure smooth product approvals.
Key Responsibilities:
✔ Prepare and submit regulatory documentation for product registrations.
✔ Ensure compliance with national and international regulations (US FDA, WHO, etc.).
✔ Communicate with regulatory authorities for approvals and queries.
✔ Maintain up-to-date knowledge of changing regulatory guidelines.
✔ Collaborate with cross-functional teams (R&D, Quality, Manufacturing).
Qualifications & Skills:
- Bachelor’s degree in Pharmacy, Chemistry, or Life Sciences.
- Strong knowledge of regulatory affairs and compliance.
- Experience in dossier submissions (ANDAs, DMFs, etc.) is a plus.
- Attention to detail and analytical skills.
- Excellent written and verbal communication.
Why Join Crius Life Sciences?
✅ Work with a US FDA & WHO-certified company.
✅ Opportunity to grow in the nutraceutical and pharmaceutical industry.
✅ Collaborative and professional work environment.
How to Apply?
Interested candidates can email their resume to:
📧 hroffice@criuslife.com
Subject Line: “Application for DRA Executive – Chandigarh”
