Job Description

Roles and Responsibilities Responsibilities:- 1. Responsible for development of stable and robust formulations across various dosage forms 2. Formulation excipient screening, stability compatibility studies, bio-analytical characterization, pharmaceutical testing, and formulation transfer to pilot- and GMP production. 3. Conducting the trouble-shooting of formulations/products in terms of composition (formulation) and process (method of manufacturing) issues 4. Applying design of experiments (DOE) in developing formulations and processes according to FDAs Quality by Design (QBD) requirements 5. Carrying out the pre formulation and formulation development studies for the selected drug candidates to support NDA and ANDA filings topical formulations 6. Conducting formulation development projects strategic discussions Developing improved (efficacious, stable and safe) formulations of drugs using novel drug delivery technologies 7. Supervising the daily work of assigned associates and also contributing to interdisciplinary development teams 8. Preparation of formulation development protocols, clinical batch manufacturing documents and technology transfer dossier (TTD). 9. Responsible for the documentation of formulation development (PDRs) and the generation of technical reports to support technical transfers and clinical trial applications. Hands on experience on equipment\'s and planning of exhibit batches.
Desired Candidate Profile

5-8 year experience in formulation development of tablet and capsules dosage form for regulated market.

Role:Formulation Scientist Salary: 5,00,000 - 8,00,000 P.A. Industry:Pharmaceutical & Life Sciences Department:Research & Development Role Category:Pharmaceutical & Biotechnology Employment Type:Full Time, Permanent

Key Skills
Tabletsandacapsules dosageNDAcapsules
Skills highlighted with \xe2\x80\x98\xe2\x80\x98 are preferred keyskills
Education PG:M.Pharma in Pharmacy

Company Profile

Marksans Pharma
Marksans Pharma, headquartered at Mumbai (India) is a global pharmaceutical company. We are actively engaged in R&D and offer CRAMS to global pharmaceutical companies. We have established world-class manufacturing facilities by leveraging state-of-the-art technology, incorporating best practices and adhering to stringent regulatory compliances. Our plants are approved by prestigious US FDA, UK MHRA, Australian TGA and other foreign health authorities. Our R&D capabilities include dossier development, chemical synthesis, process optimization, formulation development, analytical development and conducting stability studies. We have a team of over 50 experienced scientists specializing in formulation development and analytical development. We possess end-to-end capabilities from Lab scale development to Pilot scale up and from commercializing the product for large scale manufacturing to marketing globally. The company has achieved global recognition within a very short span of time and has major global expansion plans for the near future.