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14 jobs found for Drug Regulatory Affairs Director Manager

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  • knowledge of global and Indian regulatory requirements 3 - 5 years in regulatory affairs in apharmaceutical industry in an MNC. inputs for the preparation and submission of dossiers, MAA (Marketing Authorization Applications) for new drugs ...

  • knowledge of global and Indian regulatory requirements 3 - 5 years in regulatory affairs in apharmaceutical industry in an MNC. inputs for the preparation and submission of dossiers, MAA (Marketing Authorization Applications) for new drugs ...

  • knowledge of global and Indian regulatory requirements 3 - 5 years in regulatory affairs in apharmaceutical industry in an MNC. inputs for the preparation and submission of dossiers, MAA (Marketing Authorization Applications) for new drugs ...

  • knowledge of global and Indian regulatory requirements 3 - 5 years in regulatory affairs in apharmaceutical industry in an MNC. inputs for the preparation and submission of dossiers, MAA (Marketing Authorization Applications) for new drugs ...

  • knowledge of global and Indian regulatory requirements 3 - 5 years in regulatory affairs in apharmaceutical industry in an MNC. inputs for the preparation and submission of dossiers, MAA (Marketing Authorization Applications) for new drugs ...

  • knowledge of global and Indian regulatory requirements 3 - 5 years in regulatory affairs in apharmaceutical industry in an MNC. inputs for the preparation and submission of dossiers, MAA (Marketing Authorization Applications) for new drugs ...

  • knowledge of global and Indian regulatory requirements 3 - 5 years in regulatory affairs in apharmaceutical industry in an MNC. inputs for the preparation and submission of dossiers, MAA (Marketing Authorization Applications) for new drugs ...

  • Develop/Review content and format for regulatory submissions for investigational new drugs/ clinical trial applications and related supplements / amendments for completeness and compliance Experience in Global Regulatory submissions (For NCE) e.g. India DCGI, US-IND, EU-CTA filings Detailed knowledge of ICH, EU and FDA regulations and guidance for drugs Understanding of non-clinical / clinical sections of ...

  • Develop/Review content and format for regulatory submissions for investigational new drugs/ clinical trial applications and related supplements / amendments for completeness and compliance Experience in Global Regulatory submissions (For NCE) e.g. India DCGI, US-IND, EU-CTA filings Detailed knowledge of ICH, EU and FDA regulations and guidance for drugs Understanding of non-clinical / clinical sections of ...

  • Develop/Review content and format for regulatory submissions for investigational new drugs/ clinical trial applications and related supplements / amendments for completeness and compliance Experience in Global Regulatory submissions (For NCE) e.g. India DCGI, US-IND, EU-CTA filings Detailed knowledge of ICH, EU and FDA regulations and guidance for drugs Understanding of non-clinical / clinical sections of ...

  • We have 2 openings as given below: 1. Regulatory Affairs Manager (ROW Markets) We are urgently hiring for Manager Regulatory Affairs for a fast growing Pharma co. for their HQ located at Chandivali, Mumbai . Please find the details below: Company Name: Fast Growing Pharma Co. Requirement: 1 Please refer the given job description for detailed information

  • in development of Medical Strategy, Service profile and Delivery strategies Assist MS in driving empanelled Consultant Management Ensure proper allocation of paramedical and support staff to all departments in the hospital Recommendation of specified equipment and materials, drugs / medicines that have been

  • in development of Medical Strategy, Service profile and Delivery strategies Assist MS in driving empanelled Consultant Management Ensure proper allocation of paramedical and support staff to all departments in the hospital Recommendation of specified equipment and materials, drugs / medicines that have been

  • in development of Medical Strategy, Service profile and Delivery strategies Assist MS in driving empanelled Consultant Management Ensure proper allocation of paramedical and support staff to all departments in the hospital Recommendation of specified equipment and materials, drugs / medicines that have been

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