21.05.24 | Vollzeit | Augsburg | Formycon AGPartners and CDMOs. Your reporting line is to the VP Regulatory Affairs and Quality Management. Your main tasks include the following Align RA CMC DP strategy for Formycon’s development projects and approved products (focus on aseptically manufactured parenteral products in various dosage forms
Später ansehen21.05.24 | Vollzeit | Augsburg | Formycon AGPartners and CDMOs. Your reporting line is to the VP Regulatory Affairs and Quality Management. Your main tasks include the following Align RA CMC DP strategy for Formycon’s development projects and approved products (focus on aseptically manufactured parenteral products in various dosage forms
Später ansehen21.05.24 | Vollzeit | Augsburg | Formycon AGPartners and CDMOs. Your reporting line is to the VP Regulatory Affairs and Quality Management. Your main tasks include the following Align RA CMC DP strategy for Formycon’s development projects and approved products (focus on aseptically manufactured parenteral products in various dosage forms
Später ansehen21.05.24 | Vollzeit | Augsburg | Formycon AGPartners and CDMOs. Your reporting line is to the VP Regulatory Affairs and Quality Management. Your main tasks include the following Align RA CMC DP strategy for Formycon’s development projects and approved products (focus on aseptically manufactured parenteral products in various dosage forms
Später ansehen21.05.24 | Vollzeit | Augsburg | Formycon AGPartners and CDMOs. Your reporting line is to the VP Regulatory Affairs and Quality Management. Your main tasks include the following Align RA CMC DP strategy for Formycon’s development projects and approved products (focus on aseptically manufactured parenteral products in various dosage forms
Später ansehen21.05.24 | Vollzeit | Augsburg | Formycon AGPartners and CDMOs. Your reporting line is to the VP Regulatory Affairs and Quality Management. Your main tasks include the following Align RA CMC DP strategy for Formycon’s development projects and approved products (focus on aseptically manufactured parenteral products in various dosage forms
Später ansehen21.05.24 | Vollzeit | Augsburg | Formycon AGPartners and CDMOs. Your reporting line is to the VP Regulatory Affairs and Quality Management. Your main tasks include the following Align RA CMC DP strategy for Formycon’s development projects and approved products (focus on aseptically manufactured parenteral products in various dosage forms
Später ansehen21.05.24 | Vollzeit | Fürstenfeldbruck | Daiichi Sankyo Europe GmbHExpectedness and relatedness. Lead internal and external (especially regulatory, but also expert advisory) interactions to ensure quality outcomes in the risk evaluation and management of assigned projects/products. Define and implement strategies and action plans for identifying and managing risks throughout
Später ansehen21.05.24 | Vollzeit | Erding | Daiichi Sankyo Europe GmbHExpectedness and relatedness. Lead internal and external (especially regulatory, but also expert advisory) interactions to ensure quality outcomes in the risk evaluation and management of assigned projects/products. Define and implement strategies and action plans for identifying and managing risks throughout
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