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Leben Life Sciences Pvt. Ltd. invites applications for its R&D Formulation Development team at its Akola facility in Maharashtra. The Sr.
Executive/Asst. Manager will design, develop, and optimize solid and semi-solid dosage forms while ensuring EU-GMP compliance and regulatory alignment. The role requires 6–10 years of experience in formulation development and a B.Pharm or M.Pharm degree. Collaboration with cross-functional teams and rigorous documentation are essential for successful product
Leben Life Sciences R&D Sr. Executive/Asst. Manager B Pharm/M.Pharm Akola
Leben Life Sciences hiring B Pharm/M.Pharm for R&D (Formulation Development) in Akola. 6–10 yrs experience in solid & semi-solid dosage forms.
Leben Life Sciences Pvt. Ltd., a leading pharmaceutical formulation company with over four decades of excellence, invites applications for its R&D Formulation Development team at its EU-GMP approved OSD & Semi-solids manufacturing facility in Akola, Maharashtra. This is an exceptional opportunity for experienced pharmaceutical professionals to contribute to innovative drug formulation projects and strengthen their careers in a global-standard environment.
Leben Life Sciences (LLS) is renowned for its high-quality pharmaceutical formulations, spanning oral solid dosage (OSD) and semi-solid products. With a legacy of over 40 years, LLS has established itself as a trusted name in both domestic and international pharmaceutical markets.
Key Highlights:
The R&D (Formulation Development) position as Sr. Executive/Assistant Manager involves designing, developing, and optimizing pharmaceutical formulations. Candidates will work closely with cross-functional teams to ensure successful product development and regulatory compliance.
Primary Responsibilities:
Skills & Competencies:
Relevant Courses: B Pharm, M.Pharm, Pharmaceutical Sciences, Formulation Development, Drug Product Development, Solid Dosage, Semi-Solid Dosage.
Q1: Who can apply for this position?
A1: B Pharm or M.Pharm professionals with 6–10 years of experience in solid and semi-solid formulation development.
Q2: What is the job location?
A2: Akola, Maharashtra, India.
Q3: What are the main responsibilities?
A3: Formulation development, optimization, documentation, and cross-functional collaboration to ensure EU-GMP compliance.
Q5: Is prior experience in OSD & semi-solid dosage forms mandatory?
A5: Yes, experience in these dosage forms is required.