🚀Unlock Your Career in Regulatory Affairs at Leben Life Sciences

Leben Life Sciences Pvt. Ltd. (LLS) is a renowned pharmaceutical formulation company with over four decades of experience in the industry. They’re currently hiring for a Trainee position in the Regulatory Affairs department at their EU-GMP approved manufacturing facility in Akola, Maharashtra.

About the Role

As a Trainee in Regulatory Affairs, you’ll play a crucial role in ensuring compliance with regulatory requirements and guidelines. You’ll work closely with the regulatory team to gain hands-on experience in regulatory affairs and contribute to the company’s mission of providing high-quality pharmaceutical products.

Responsibilities

While the specific responsibilities for this role may vary, you can expect to:

Assist the regulatory team in preparing and submitting regulatory documents

Ensure compliance with regulatory requirements and guidelines

Collaborate with cross-functional teams to ensure regulatory compliance

Gain hands-on experience in regulatory affairs

Requirements

Qualification: M. Pharm degree

Experience: 0 to 1 year of experience

Skills: Strong knowledge of regulatory affairs and guidelines

What We Offer

Opportunity to work with a leading pharmaceutical company

Hands-on experience in regulatory affairs

Collaborative and dynamic work environment

📮 How to Apply

Interested candidates can send their resumes to:

📧 career@lebenlifesciences.com

📞 7498035480

Take your first step toward a rewarding career in Regulatory Affairs! 🌱✨

Why Choose Leben Life Sciences?

Leben Life Sciences is committed to responsible healthcare and has a strong reputation for quality and compliance. By joining their team, you’ll have the opportunity to contribute to the development of high-quality pharmaceutical products and grow your career in a dynamic and supportive environment.

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