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Programme Coordinator | Cadila Pharmaceuticals Limited | Ahmedabad, India
Written by MiJobz 75217202     January 10, 2014    
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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 six decades, it has been developing and manufacturing pharmaceutical products and selling and distributing these in over 90 countries around the world.

Career Opportunity at Cadila Pharmaceuticals Limited

The company focuses on providing high quality, appropriately priced products to its customers and supports all these with dedicated customer service. Cadila Pharmaceuticals has a multicultural, multilingual and multinational workforce of more than seven thousand employees including over two hundred people outside India. At Cadila Pharmaceuticals your career and growth enhancement is comprehensive in a knowledge driven work environment.

Contact Details

Cadila Pharmaceuticals Limited

Services Offered

Services Offered
Provider with pharmaceutical product basket. It caters to over 45 therapeutic areas that include:
• Cardiovascular
• Gastrointestinal
• Analgesics
• Haematinics
• Anti infective
• Antibiotics
• Respiratory agents
• Anti diabetics
• Immunologicals

Salary Offered

Salary Offered
Please Inquire

Job Application Contact Details

Phone Number
+91 2718 225 001

Qualifications & Experience Required

Qualifications & Experience
• UG - Any Graduate - Any Specialization, Graduation Not Required
• PG - Any Postgraduate - Any Specialization, Post Graduation Not Required
• DOCTORATE - Any Doctorate - Any Specialization, Doctorate Not Required

Job Description:
• Specialty in manufacturing / supply chain US FDA Plant.
• Experience in product development will be helpful Not necessary
• Must have the experience of supplying the products to US
• Responsible for Product Identification / Product Development / Product Registration and Product Distribution in North America.
• Hard-core techno-commercial business development.
• To coordinate with 3rd party for supplying of ANDA products for distribution in North America.
• Provide regulatory strategy to cross functional teams of R&D, Quality and manufacturing for successful and timely filing of ANDAs in N. America.
• Provide key inputs to cross functional teams during development of ANDA products.
• Manage the registration of generic small molecule products in the N. America.
• Review drug development documents to ensure it meets regulatory requirement

Required skills set:
• Excellent Analytic Abilities
• Strong Communication
• Interpersonal Skills

• Experience : 5 - 10 Years
• Industry : Pharma / Biotech / Clinical Research
• Role : Research Scientist
• Functional Area: Medical, Healthcare, R&D, Pharmaceuticals, Biotechnology

Method of Application

Is a MiJobz Profile Required to Apply?
Not strictly, but a MiJobz profile is a significant advantage
Can Candidates Apply by Phone?
Swap Start/End

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