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Drug Development Coordination Lead
9 hours ago
Job Description
Company Overview
TFS HealthScience is a global Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey.
Job Summary
The Drug Substance Outsourcing Manager is responsible for leading and coordinating the outsourcing of drug substance development and manufacturing activities, ensuring optimal supplier relationships and alignment with operational and strategic goals.
Main Responsibilities:
- Lead and coordinate drug substance outsourcing activities, including vendor identification, evaluation, and selection.
- Build and maintain strong relationships with Contract Development and Manufacturing Organizations (CDMOs) to ensure efficiency, quality, and compliance.
- Manage outsourced projects, ensuring deliverables are met on time, within budget, and according to quality standards.
- Negotiate contracts and budgets to ensure cost-effective and high-quality outcomes.
- Ensure adherence to regulatory requirements, Good Manufacturing Practices (GMP), and company policies.
- Partner with internal teams such as R&D, Quality Assurance, and Regulatory Affairs to align on project goals and timelines.
Requirements:
- Education: A degree in life sciences, biotechnology, or a related field (advanced degree preferred).
- Experience:
- Minimum of 5 years of experience in drug substance manufacturing and outsourcing.
- Proven experience managing CDMO partnerships in the biotechnology or pharmaceutical industry.
- Knowledge:
- In-depth understanding of biologics manufacturing processes, GMP requirements, and global regulatory frameworks, especially in the Nordics.
- Skills:
- Strong project management and organizational skills.
- Excellent negotiation and communication abilities.
- Ability to work cross-functionally and build strong relationships with internal and external stakeholders.
- Language Proficiency: Fluency in English is required; knowledge of Swedish is a plus.
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