
51 - 200 employees
💼 Consulting
🏥 Healthcare
🧬 Biotechnology
Consulting • Healthcare • Biotechnology
MAIN5 is a consulting firm that specializes in driving digital transformation in the Life Sciences sector. With a team of over 60 dedicated professionals, MAIN5 focuses on delivering innovative solutions through strategic development, organizational consulting, regulatory affairs, and quality management. The company prides itself on its commitment to excellence and expertise, helping clients navigate the complexities of the life science industry while embracing cutting-edge technologies and best practices in areas such as change management and compliance.
🕒 June 10
🗣️🇩🇪 German Required
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51 - 200 employees
💼 Consulting
🏥 Healthcare
🧬 Biotechnology
Consulting • Healthcare • Biotechnology
MAIN5 is a consulting firm that specializes in driving digital transformation in the Life Sciences sector. With a team of over 60 dedicated professionals, MAIN5 focuses on delivering innovative solutions through strategic development, organizational consulting, regulatory affairs, and quality management. The company prides itself on its commitment to excellence and expertise, helping clients navigate the complexities of the life science industry while embracing cutting-edge technologies and best practices in areas such as change management and compliance.
• Take responsibility for one or more projects • Lead a project team and ensure that expectations are met • Introduce and implement best practices and methodologies to create value for the client • Conduct workshops, gather requirements, manage vendor selection and execute data migrations • Act as the liaison between the company and software vendors • Improve business processes • Promote a culture of knowledge sharing • Identify and propose opportunities to improve team performance
• More than 5–8 years of experience in the pharmaceutical industry • Expertise in Regulatory Operations and Regulatory Information Management • Deep understanding of regulatory processes and data • Expert in data management, including Data Governance and Master Data Management • Practical experience with xEVMPD and IDMP • Knowledge of relevant guidance, such as the EU IDMP Implementation Guide • Experience implementing and operating RIM systems • Development and execution of data migration strategies • Strong affinity for both business and technology
• Attractive compensation with bonus opportunities • Flexible working hours & remote work options • State-of-the-art equipment for office and remote work • Creative working environment & inspiring events • Regular international team meetings & company events • Secure position with long-term prospects
Apply Now🕒 March 31
Lead R&D consulting initiatives at Veeva, a life sciences innovator, building customer networks and managing project deliveries across Europe.