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    Marco Brose

    Regulatory&CMC Manager bei CSL Behring Innovation GmbH

    Professional Background

    Marco Brose is a highly regarded professional in the field of biotechnology and pharmaceuticals, bringing extensive experience in regulatory affairs and project management. Presently, Marco serves as the Regulatory & CMC Manager at CSL Behring Innovation GmbH, where he leverages his expertise to navigate complex regulatory landscapes, ensuring compliance and optimizing the development processes of innovative biopharmaceutical products.

    Prior to his current role, Marco honed his skills at CSL Behring, where he also held the position of Regulatory & CMC Manager. His tenure at CSL Behring has been marked by his deep understanding of regulatory submissions and lifecycle management, allowing for effective cross-functional collaboration, which is crucial in the biopharmaceutical industry. Marco's role involves working closely with teams to develop strategies that meet regulatory requirements while also driving projects toward successful completion.

    Before his impactful journey at CSL Behring, Marco held several key positions in the pharmaceutical landscape. His experience at GSK as a Program Manager equipped him with vital knowledge in the management of drug development programs, where he ensured efficient project delivery while overseeing compliance with regulatory standards. His role at Novartis Vaccines and Diagnostics further enriched his background, as he served as Project Manager, offering insight into vaccine development processes that are vital for public health.

    Marco began his career as a Project Associate and Process Expert at Crucell, where he developed a strong foundation in project management within the biotechnology sector. His technical expertise was further solidified during his role as a Project Engineer at NNE Pharmaplan, where he was responsible for designing and implementing solutions in the pharmaceutical manufacturing domain. Marco's diverse career has provided him with a multifaceted perspective on biopharmaceutical development, making him a valuable asset in any organization.

    Education and Achievements

    Marco Brose's educational background is impressive and serves as the backbone of his comprehensive skill set. He began his higher education at Hochschule Mannheim, where he studied Diplom in Biotechnologie, paving the way for his deep understanding of biological systems and the applications of biotechnology in industry. Following this, Marco further specialized in Polymer-/Kunststofftechnik at Fachhochschule Darmstadt, augmenting his expertise in materials science, which is crucial in developing biopharmaceutical products.

    Throughout his career, Marco has consistently demonstrated a commitment to professional development and continuous learning. His academic achievements, combined with hands-on experience, empower him to contribute significantly to the fields of regulatory affairs, project management, and pharmaceutical development.

    Achievements

    Throughout his successful career, Marco has achieved numerous milestones that underscore his expertise in the field. At CSL Behring, his contributions to regulatory affairs have not only facilitated the approval of critical biopharmaceutical products but have also set best practices within the company, enhancing the overall process efficiency.

    His strategic approach to project management at GSK led to the timely completion of several key programs, further establishing him as a reliable leader who can deliver results. Marco’s role in vaccine development with Novartis Vaccines and Diagnostics has played a significant part in advancing public health initiatives, demonstrating his commitment to making a positive impact in the biopharmaceutical industry.

    Marco Brose's journey from academia to leadership roles in well-established pharmaceutical organizations exemplifies his dedication to the field of biotechnology. His combination of educational prowess and practical experience makes him a distinguished professional capable of navigating the intricacies of the biopharmaceutical landscape. Through his various roles, Marco has not only contributed to the success of his organizations but has also played a vital role in the advancement of healthcare solutions globally.

    Related Questions

    How did Marco Brose develop his expertise in regulatory affairs within the pharmaceutical industry?
    What insights has Marco gained from his experiences at CSL Behring as a Regulatory & CMC Manager?
    In what ways has Marco's background in Polymer-/Kunststofftechnik influenced his approach to project management in biotechnology?
    What key projects did Marco manage during his time at GSK that contributed to his professional growth?
    How has Marco Brose's education at Hochschule Mannheim and Fachhochschule Darmstadt shaped his career in biotechnology?
    Marco Brose
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    Location

    Marburg an der Lahn, Hesse, Germany