DRA

Postgraduate degree in life sciences, pharmacy, biotechnology, clinical research, regulatory affairs or other relevant discipline from a recognized university, with at least 5 years of relevant experience in project or program management

Plan, track, and deliver submissions aligned with timelines and regulatory requirements. Manage risks, dependencies, and complexities in global regulatory environments.

Full-time B-Pharma & M-Pharma -Batch of 2024 & 2025 from a recognized university / college. Should be open to work in any shifts

Regulatory Affairs (Pharmaceuticals & Medical Devices) Quality Management System (QMS)Medical Device Licensing and Compliance 

Experienced Shift In Charge to Manage daily manufacturing Operations, ensuring strict cGMP, Safety and regulatory Compliance. Key duties include production planning & ensuring execution as per plan, preparing batch records and qualification documents.

PhD in any branch of Life Sciences / Agricultural Biotechnology / Food and Nutrition Sciences/ Food Technology or equivalent

Strong organizational and negotiation skills, detail-oriented, ability to adapt to a fast-paced and changing environment

Leben Life Sciences Pvt. Ltd. is an established pharmaceutical formulation company for more than four decades. M.Pharm freshers can apply for Apprentice

Seeking a highly experienced Regulatory Affairs professional to manage regulatory activities for parenteral (injectable) products across the LATAM region.