Leben Life Sciences Pvt. Ltd., a trusted pharmaceutical formulation company with over 40 years of expertise, is hiring Regulatory Affairs Trainees for its EU-GMP approved OSD & Semi-Solids manufacturing facility in Akola, Maharashtra.
This is an excellent opportunity for fresh M.Pharm graduates looking to begin a career in Regulatory Affairs, gain hands-on exposure, and work in a global-standard pharma environment.
Key Responsibilities
As a Regulatory Affairs Trainee, you will be trained in and responsible for:
- Assisting in the preparation, review, and submission of regulatory documents
- Supporting regulatory compliance activities across product lifecycle
- Coordination with manufacturing, QA, QC, and documentation teams
- Maintaining regulatory databases and tracking submissions
- Ensuring adherence to global regulatory guidelines
- Preparing product dossiers for different regulatory markets
- Assisting in audit readiness activities
Eligibility Criteria
Designation: Regulatory Affairs Trainee
Qualification:
- M. Pharm (Mandatory)
Experience:
- 0–1 year (Freshers eligible)
Preferred Candidates:
- Male candidates, as mentioned by the organization
- Strong communication and documentation skills
- Interest in global regulatory systems and dossier preparation
Why Join Leben Life Sciences?
- Work in an EU-GMP approved, global-standard pharma facility
- Exposure to OSD and Semi-solid formulations
- Learn regulatory documentation aligned with international markets
- Professional career growth in a rapidly expanding organization
- Supportive learning environment for fresh graduates
Job Location
📍 Akola, Maharashtra (M.S.)
Leben Life Sciences Pvt. Ltd. – OSD & Semi-Solid Manufacturing Facility
How to Apply
Interested candidates can send their updated resume to:
📧 career@lebenlifesciences.com
📞 7498035480
