Mylan is one of the world’s leading generics and specialty pharmaceutical companies, providing products to customers in more than 150 countries and territories. The company maintains one of the industry’s broadest and highest quality product portfolios, which is regularly bolstered by an innovative and robust product pipeline. With a workforce of more than 16,000, Mylan has attained leading positions in key international markets through its wide array of dosage forms and delivery systems, significant manufacturing capacity, global commercial scale and a committed focus on quality and customer service.
Post: Manager – Regulatory Affaires
Job Description:
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Developing good communication network with drug regulatory authorities and coordinating with drug authorities for the registration of drugs/ renewal of certificates
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Providing periodic updates of the interactions with the authorities
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Maintaining record of existing licenses & dates for renewal of each; applying for renewals well in time
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Preparing a framework with timelines for the registration of new products
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Reviewing and approve the artwork for label and cartons
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Prepare the prescribing information and abbreviated prescribing information for the products
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Having complete understanding of the drug laws existing in the country
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Developing & complying with local SOP
Qualifications
Make Our Values Your Values
Mylan hires only the best. People who thrive in a culture of innovation and empowerment. People who are active learners and have a positive attitude. People who are leaders and know that by working together we can run faster, reach higher and achieve more. By doing so, we will continue to set new standards in health care. Here are the qualifications for this position:
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Minimum 5-10 years Experience
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Bachelors degree in Pharmacy and Masters degree in Pharmarcy or Masters degree in Science
Additional Information:
Experience: 5-10 year
Location: Andhra Pradesh-Hyderabad
Industry Type: Pharma/Biotech/Clinical Research
Functional Area: R&D
End Date: 17th Oct, 2013
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