Leben Life Sciences Hiring Sr. Officer – Regulatory Affairs

M.Pharm Regulatory Affairs Job Opening at EU-GMP Approved Facility in Akola, Maharashtra

M.Pharm holders with 3-4 years of experience apply for Regulatory Affairs Sr. Officer role at Leben Life Sciences, Akola, Maharashtra. EU-GMP facility.

Join Leben Life Sciences – A Trusted Name in Global Pharmaceutical Manufacturing

Leben Life Sciences Pvt. Ltd. (LLS), a well-established pharmaceutical formulation company with over four decades of industry excellence, is expanding its team. Known for its EU-GMP approved OSD and semi-solid formulation facility in Akola, Maharashtra, the company is currently hiring for a crucial role in the Regulatory Affairs Department.

Job Opening: Sr. Officer – Regulatory Affairs

Location: Akola, Maharashtra
Department: Regulatory Affairs
Experience Required: 3 to 4 years in Regulatory Affairs
Qualification: M.Pharm (Master of Pharmacy)

Key Responsibilities

• Preparation, submission, and life-cycle management of regulatory dossiers for semi-solid and solid oral dosage forms.
• Understanding global regulatory guidelines and requirements for product registration in emerging and regulated markets.
• Collaborate with R&D, Quality Assurance, and Manufacturing for timely documentation.
• Respond to queries from regulatory authorities and coordinate with third parties for submissions.
• Keep updated records and ensure regulatory compliance at all levels.

Why Join Leben Life Sciences?

• Work in a EU-GMP approved manufacturing facility.
• Contribute to a company with 40+ years of pharmaceutical innovation.
• Excellent opportunity for growth and global regulatory exposure.
• Be part of a high-performing, mission-driven team focused on responsible healthcare.

Application Process

Interested and eligible candidates may share their updated resumes to:
career@lebenlifesciences.com
Contact: +91 7498035480
Website: www.lebenlifesciences.com

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