Empleos de regulatory en Estado de Oaxaca

A leading biotechnology firm is seeking an Executive Director for Medical Writing in Oaxaca, Mexico. The successful candidate will establish and oversee the Cardiorenal Medical Writing group, ensuring high-quality regulatory and clinical documents. They will lead the writing processes from concept to final product and mentor medical writers. Candidates should possess a post-graduate degree and...

Role Summary The Vice President, Regulatory Affairs will oversee BridgeBio’s Operations and Labeling functions, and will also support regulatory strategy as needed. This leader will manage a team of subject matter experts and leaders responsible for Regulatory Operations, Regulatory Business Operations, and Labeling, ensuring excellence, compliance, and strategic alignment across all regulatory...

A leading biotechnology firm is seeking a Senior Manager for Global Regulatory Affairs Strategy. The role involves providing regulatory strategy support, managing regulatory submissions, and interacting with health authorities. Candidates must hold a Bachelor's degree in a scientific discipline, have at least 5 years of regulatory affairs experience, and possess strong skills in project...

A biotechnology company in Mexico is seeking an Associate Director of Regulatory Affairs. This role involves developing and executing global regulatory strategies for product development and leading interactions with major health authorities. Candidates should have a strong background in regulatory affairs within the pharmaceutical industry, with extensive experience in preparing major regulatory...

A leading biotechnology firm is seeking a Senior Manager for Global Regulatory Affairs Strategy. The role involves providing regulatory strategy support, managing regulatory submissions, and interacting with health authorities. Candidates must hold a Bachelor's degree in a scientific discipline, have at least 5 years of regulatory affairs experience, and possess strong skills in project...

A biotechnology company in Mexico is seeking an Associate Director of Regulatory Affairs. This role involves developing and executing global regulatory strategies for product development and leading interactions with major health authorities. Candidates should have a strong background in regulatory affairs within the pharmaceutical industry, with extensive experience in preparing major regulatory...

A biopharmaceutical company in Oaxaca seeks a Vice President of Regulatory Affairs to oversee all regulatory operations and labeling functions. The role requires an advanced degree and over 15 years of regulatory experience in the biopharmaceutical sector. The VP will manage a team and ensure compliance across all regulatory activities while promoting innovation through AI integration. The ideal...

A leading biotechnology company is seeking a Senior Director of Regulatory Affairs in Oaxaca, Mexico. The ideal candidate will have over 15 years of experience in regulatory leadership, specializing in strategic development and execution of regulatory submissions. This hybrid role requires expertise in navigating interactions with global health authorities and leading cross-functional teams. The...

Role Summary The Vice President, Regulatory Affairs will oversee BridgeBio’s Operations and Labeling functions, and will also support regulatory strategy as needed. This leader will manage a team of subject matter experts and leaders responsible for Regulatory Operations, Regulatory Business Operations, and Labeling, ensuring excellence, compliance, and strategic alignment across all regulatory...

A leading biotechnology company is seeking a Senior Director of Regulatory Affairs in Oaxaca, Mexico. The ideal candidate will have over 15 years of experience in regulatory leadership, specializing in strategic development and execution of regulatory submissions. This hybrid role requires expertise in navigating interactions with global health authorities and leading cross-functional teams. The...

A biopharmaceutical company in Oaxaca seeks a Vice President of Regulatory Affairs to oversee all regulatory operations and labeling functions. The role requires an advanced degree and over 15 years of regulatory experience in the biopharmaceutical sector. The VP will manage a team and ensure compliance across all regulatory activities while promoting innovation through AI integration. The ideal...

A leading biotechnology firm is seeking an Executive Director for Medical Writing in Oaxaca, Mexico. The successful candidate will establish and oversee the Cardiorenal Medical Writing group, ensuring high-quality regulatory and clinical documents. They will lead the writing processes from concept to final product and mentor medical writers. Candidates should possess a post-graduate degree and...

A global biotech company in San Francisco is seeking an Associate Director for Regulatory Affairs CMC to develop and execute regulatory strategies. The ideal candidate should have at least 8 years of experience in clinical research or pharmaceuticals and a strong background in global CMC regulatory processes. This role involves collaborating with cross-functional teams, ensuring compliance with...

Role Summary Associate Director, Regulatory Affairs CMC, reporting to the Senior Director, Regulatory Affairs CMC, responsible for developing and executing CMC regulatory strategies for Olema products in development and post-approval. Ensure strategies align with Health Authority requirements globally and provide guidance for high-quality, on-time CMC sections of regulatory submissions, plus...

Role Summary The Associate Director, Regulatory Affairs will be responsible for developing and delivering innovative, breakthrough global regulatory strategies for product development and approval, in alignment with the global business strategy. Responsible for leading a comprehensive and strategic approach to developing and executing integrated global regulatory strategies that account for the...

Role Summary As the Senior Manager, Global Regulatory Affairs Strategy, reporting to the Senior Director, Global Regulatory Affairs Strategy, you will provide regulatory strategy support in partnership with cross functional teams and subject matter experts and manage regulatory aspects through all phases of development. You will represent Regulatory Affairs on cross-functional teams, lead the...

A global biotech company in San Francisco is seeking an Associate Director for Regulatory Affairs CMC to develop and execute regulatory strategies. The ideal candidate should have at least 8 years of experience in clinical research or pharmaceuticals and a strong background in global CMC regulatory processes. This role involves collaborating with cross-functional teams, ensuring compliance with...

Role Summary Associate Director, Regulatory Affairs CMC, reporting to the Senior Director, Regulatory Affairs CMC, responsible for developing and executing CMC regulatory strategies for Olema products in development and post-approval. Ensure strategies align with Health Authority requirements globally and provide guidance for high-quality, on-time CMC sections of regulatory submissions, plus...

Role Summary The Associate Director, Regulatory Affairs will be responsible for developing and delivering innovative, breakthrough global regulatory strategies for product development and approval, in alignment with the global business strategy. Responsible for leading a comprehensive and strategic approach to developing and executing integrated global regulatory strategies that account for the...

Role Summary As the Senior Manager, Global Regulatory Affairs Strategy, reporting to the Senior Director, Global Regulatory Affairs Strategy, you will provide regulatory strategy support in partnership with cross functional teams and subject matter experts and manage regulatory aspects through all phases of development. You will represent Regulatory Affairs on cross-functional teams, lead the...