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27 jobs found for Drug Regulatory Affairs Director Manager

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  • 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

  • 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

  • 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

  • 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

  • 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

  • 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 ...

  • complex problems and offer effective solutions through development or modification of test methodology. Expertise in handling and optimizing most highly variable molecules designed. Skills in ensuring product delivery on target timelines. Familiarity with QBD project management methodology. Demonstrated

  • complex problems and offer effective solutions through development or modification of test methodology. Expertise in handling and optimizing most highly variable molecules designed. Skills in ensuring product delivery on target timelines. Familiarity with QBD project management methodology. Demonstrated

  • statutes and General Meetings and to maintain the minutes of these meetings. 3. To advise the Board of Directors on regulatory, procedural and corporate governance related matters. 4. To ensure that affairs of the company are managed in accordance with its objects contained in the Memorandum and Articles

  • statutes and General Meetings and to maintain the minutes of these meetings. 3. To advise the Board of Directors on regulatory, procedural and corporate governance related matters. 4. To ensure that affairs of the company are managed in accordance with its objects contained in the Memorandum and Articles

  • statutes and General Meetings and to maintain the minutes of these meetings. 3. To advise the Board of Directors on regulatory, procedural and corporate governance related matters. 4. To ensure that affairs of the company are managed in accordance with its objects contained in the Memorandum and Articles

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