21.05.24 | Vollzeit | Unterschleißheim | Daiichi Sankyo Europe GmbHThe product life cycle. Effectively coordinate and manage available resources in developing and delivering high-quality safety evaluation related documents/deliverables on time. Coordinate and participate actively in safety-related regulatory interactions (e.g., regulatory meetings, post-approval commitments
Später ansehen21.05.24 | Vollzeit | Unterschleißheim | Daiichi Sankyo Europe GmbHThe product life cycle. Effectively coordinate and manage available resources in developing and delivering high-quality safety evaluation related documents/deliverables on time. Coordinate and participate actively in safety-related regulatory interactions (e.g., regulatory meetings, post-approval commitments
Später ansehen21.05.24 | Vollzeit | Unterschleißheim | Daiichi Sankyo Europe GmbHThe product life cycle. Effectively coordinate and manage available resources in developing and delivering high-quality safety evaluation related documents/deliverables on time. Coordinate and participate actively in safety-related regulatory interactions (e.g., regulatory meetings, post-approval commitments
Später ansehen21.05.24 | Vollzeit | Unterschleißheim | Daiichi Sankyo Europe GmbHThe product life cycle. Effectively coordinate and manage available resources in developing and delivering high-quality safety evaluation related documents/deliverables on time. Coordinate and participate actively in safety-related regulatory interactions (e.g., regulatory meetings, post-approval commitments
Später ansehen21.05.24 | Vollzeit | Unterschleißheim | 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 | Unterschleißheim | 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 | Unterschleißheim | 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 | Unterschleißheim | 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 | Unterschleißheim | 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
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