Cadila Pharmaceuticals Ltd. is one of the largest privately held pharmaceutical companies in India, headquartered at Ahmedabad, in the State of Gujarat. Over the last seven decades, the company has been developing and manufacturing pharmaceutical products in India and selling and distributing these in over hundred other countries around the world.
Vacancy details:
- Department: Research Scientist II/Research Associate
- Qualification: M.Pharma in Any Specialization
- Experience: 2-7 Years
Important Details :
- Location: Ahmedabad( Dholka )
- Selection Process: The selection will be on the basis of Interview.
- Mode of Interview: face to face
- Interview Rounds of Interview: HR
Greetings from Cadila Pharmaceuticals Ltd..!!!!
Job Title: Research Scientist II
Department: F&D (Injection)
Location: Dholka (Ahmedabad)
Salary: 7-8LPA
Experience: 4-7 Years of Injectable Dosage Development Experience
Job Description:
- To prepare BOM for new UID activities with respect to costing of NPDs.
- To develop parenteral dosage form(injection liquid, Lyophilized) in compliance to regulatory requirments of domestic and regulatory market.
- To prepare various technology transfer documents like Master Formula card, Product development report, specification etc.
- To provide Technical Support to team for development and timely execution of the projects.
- To maintain Lab note books, stability data compilation and tracking of project progress.
- To execute the various development trials to support regulatory for query response.
- Ensure compliance of SOPs, GLP, and GDP in product development group.
Interested candidate can share there cv at shardulsinh.k@cadilapharma.com
Job Title: Research Associate
Department: F&D (Injection)
Location: Dholka (Ahmedabad)
Experience: 2-5 Years of Injectable Dosage Development Experience
Job Description:
- To prepare BOM for new UID activities with respect to costing of NPDs.
- To develop parenteral dosage form(injection liquid, Lyophilized) in compliance to regulatory requirments of domestic and regulatory market.
- To prepare various technology transfer documents like Master Formula card, Product development report, specification etc.
- To provide Technical Support to team for development and timely execution of the projects.
- To maintain Lab note books, stability data compilation and tracking of project progress.
- To execute the various development trials to support regulatory for query response.
- Ensure compliance of SOPs, GLP, and GDP in product development group.
Interested candidate can share there cv at shardulsinh.k@cadilapharma.com
