David Blanco

David Blanco

BD & PM Director

Leanbio

About me

Do you belong to a pharmaceutical or biotech company? Are you looking for a CDMO partner for Biologics? Leanbio is your trusted innovative partner: ⚙️ One-stop shop partner through supply chain and value chain ⚙️ From full development, preclinical to commercial manufacturing ⚙️ We consolidate your sales needs in a sustainable way ⚙️ Unique capabilities with combination of Microbial, Mammalian, ADCs, pDNA and mRNA ⚙️ We comply with cGMP regulations requested by EMA and FDA standards If you're seeking end-to-end integrated solutions, let's talk! About me: 15 years of experience in biotech and pharmaceuticals business development and project management including PMP certification. Proven business leader with demonstrated success managing global complex CDMO projects in the Pharma and Biotech Industry and integrating all aspects of complex industrial technology products and systems. I have experience leading and managing biotech and pharma projects focused on biologics and small molecule products, sponsor and budget management, strong commercial and technical knowledge of pharmaceutical industry, and excellent communication skills, with strong ability to build strong relationships and motivate internal teams. My role responsibility fully includes: - Leads and directs cross-functional teams - Understands and manages client requirements, expectations, and needs to achieve client objectives and satisfaction. - Collaborate with technical teams to identify risks, develop mitigation plans and escalate risks and issues. - Manage complex and multifaceted projects from clinical to commercial manufacturing. - Responsible and mentoring to team members with full supervision of their activities. - Management of business development and project management activities with our customers. - Manage a portfolio of complex initiatives that span one or multiple lines of business. - Provide on-site training and leadership for project team by building and motivating team members to meet project goals, adhering to their responsibilities and project milestones. - Work creatively and analytically in a problem-solving environment demonstrating teamwork, innovation and excellence. - Participate in establishing metrics, practices, templates, policies, tools and partnerships to expand and mature these capabilities for the organization. - Manage ongoing quality control and participate in quality issues. - Assist in dispute, negotiation, arbitration or litigation.

Interested In:

In which geographical areas you plan to expand
North America (USA, Canada)Europe - EU countries

Offering:

Offering: API
Enzymes

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