27.05.24 | Vollzeit | Landsberg am Lech | Nuclidium DE GmbHAnd support technical personnel in their daily tasks, ensuring the smooth progress of projects. Measure project progress, prepare reports, and actively contribute to the team's success. Define clear deliverables, roles, and responsibilities for team members, both internal and external. Research and evaluate
Später ansehen27.05.24 | Vollzeit | Landsberg am Lech | Nuclidium DE GmbHAnd support technical personnel in their daily tasks, ensuring the smooth progress of projects. Measure project progress, prepare reports, and actively contribute to the team's success. Define clear deliverables, roles, and responsibilities for team members, both internal and external. Research and evaluate
Später ansehen27.05.24 | Vollzeit | Landsberg am Lech | Nuclidium DE GmbHAnd support technical personnel in their daily tasks, ensuring the smooth progress of projects. Measure project progress, prepare reports, and actively contribute to the team's success. Define clear deliverables, roles, and responsibilities for team members, both internal and external. Research and evaluate
Später ansehen21.05.24 | Vollzeit | Landsberg am Lech | 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 | Landsberg am Lech | 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 | Landsberg am Lech | Daiichi Sankyo Europe GmbHAnd serving as the primary point of contact. Review and analyze data from clinical trials, post-marketing and other relevant sources for the prompt identification of safety signals. Review and evaluate serious adverse event reports from clinical trials or post-marketing for completeness, accuracy
Später ansehen21.05.24 | Vollzeit | Landsberg am Lech | Daiichi Sankyo Europe GmbHAnd serving as the primary point of contact. Review and analyze data from clinical trials, post-marketing and other relevant sources for the prompt identification of safety signals. Review and evaluate serious adverse event reports from clinical trials or post-marketing for completeness, accuracy
Später ansehen21.05.24 | Vollzeit | Landsberg am Lech | Daiichi Sankyo Europe GmbHAnd serving as the primary point of contact. Review and analyze data from clinical trials, post-marketing and other relevant sources for the prompt identification of safety signals. Review and evaluate serious adverse event reports from clinical trials or post-marketing for completeness, accuracy
Später ansehen21.05.24 | Vollzeit | Landsberg am Lech | Daiichi Sankyo Europe GmbHAnd serving as the primary point of contact. Review and analyze data from clinical trials, post-marketing and other relevant sources for the prompt identification of safety signals. Review and evaluate serious adverse event reports from clinical trials or post-marketing for completeness, accuracy
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