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41 jobs found for Drug Regulatory Affairs Director Manager

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  • w.r.t regulatory point of view. Experience in Japan accreditation by providing required documents to the PMDA through agent. Supporting the regulatory / customer audits. Knowledge on eCTD guide lines and update with the current guide lines ...

  • w.r.t regulatory point of view. Experience in Japan accreditation by providing required documents to the PMDA through agent. Supporting the regulatory / customer audits. Knowledge on eCTD guide lines and update with the current guide lines ...

  • w.r.t regulatory point of view. Experience in Japan accreditation by providing required documents to the PMDA through agent. Supporting the regulatory / customer audits. Knowledge on eCTD guide lines and update with the current guide lines ...

  • w.r.t regulatory point of view. Experience in Japan accreditation by providing required documents to the PMDA through agent. Supporting the regulatory / customer audits. Knowledge on eCTD guide lines and update with the current guide lines ...

  • w.r.t regulatory point of view. Experience in Japan accreditation by providing required documents to the PMDA through agent. Supporting the regulatory / customer audits. Knowledge on eCTD guide lines and update with the current guide lines ...

  • w.r.t regulatory point of view. Experience in Japan accreditation by providing required documents to the PMDA through agent. Supporting the regulatory / customer audits. Knowledge on eCTD guide lines and update with the current guide lines ...

  • 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

  • the key product differentiating factors based on the evidence generated in its development for promotional messaging, marketing insights and others. Maximize the value proposition of the asset/late stage portfolio through life cycle management. Provide continuous support to the cross functional teams

  • the key product differentiating factors based on the evidence generated in its development for promotional messaging, marketing insights and others. Maximize the value proposition of the asset/late stage portfolio through life cycle management. Provide continuous support to the cross functional teams

  • the key product differentiating factors based on the evidence generated in its development for promotional messaging, marketing insights and others. Maximize the value proposition of the asset/late stage portfolio through life cycle management. Provide continuous support to the cross functional teams

  • the key product differentiating factors based on the evidence generated in its development for promotional messaging, marketing insights and others. Maximize the value proposition of the asset/late stage portfolio through life cycle management. Provide continuous support to the cross functional teams

  • the key product differentiating factors based on the evidence generated in its development for promotional messaging, marketing insights and others. Maximize the value proposition of the asset/late stage portfolio through life cycle management. Provide continuous support to the cross functional teams

  • Clinnovo Provides training,internships,diploma and hands of experience in Clinical research,SAS,CDM. Clinnovo offers above aspects in Clinical Research Clinical Data Management SAS Pharmacovigilance Clinical trial management,drug regulatory affairs Needed to be passion about science. 1. Bsc, Msc,B.E bio,M tech Bio,Phd 2. Good % aggregate in school and university 3. Excellent verbal and written ...

  • Clinnovo Provides training,internships,diploma and hands of experience in Clinical research,SAS,CDM. Clinnovo offers above aspects in Clinical Research Clinical Data Management SAS Pharmacovigilance Clinical trial management,drug regulatory affairs Needed to be passion about science. 1. Bsc, Msc,B.E bio,M tech Bio,Phd 2. Good % aggregate in school and university 3. Excellent verbal and written ...

  • Clinnovo Provides training,internships,diploma and hands of experience in Clinical research,SAS,CDM. Clinnovo offers above aspects in Clinical Research Clinical Data Management SAS Pharmacovigilance Clinical trial management,drug regulatory affairs Needed to be passion about science. 1. Bsc, Msc,B.E bio,M tech Bio,Phd 2. Good % aggregate in school and university 3. Excellent verbal and written ...

  • Clinnovo Provides training,internships,diploma and hands of experience in Clinical research,SAS,CDM. Clinnovo offers above aspects in Clinical Research Clinical Data Management SAS Pharmacovigilance Clinical trial management,drug regulatory affairs Needed to be passion about science. 1. Bsc, Msc,B.E bio,M tech Bio,Phd 2. Good % aggregate in school and university 3. Excellent verbal and written ...

  • Clinnovo Provides training,internships,diploma and hands of experience in Clinical research,SAS,CDM. Clinnovo offers above aspects in Clinical Research Clinical Data Management SAS Pharmacovigilance Clinical trial management,drug regulatory affairs Needed to be passion about science. 1. Bsc, Msc,B.E bio,M tech Bio,Phd 2. Good % aggregate in school and university 3. Excellent verbal and written ...

  • Clinnovo Provides training,internships,diploma and hands of experience in Clinical research,SAS,CDM. Clinnovo offers above aspects in Clinical Research Clinical Data Management SAS Pharmacovigilance Clinical trial management,drug regulatory affairs

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