Robert Dream is a distinguished leader in the biopharmaceutical industry, bringing over 34 years of comprehensive experience that spans the full product lifecycle—from early-stage process development to large-scale commercial manufacturing. His deep expertise encompasses a diverse array of biopharmaceutical products, including vaccines, recombinant proteins, monoclonal antibodies (mAbs), and advanced therapy medicinal products (ATMPs), such as cell and gene therapies (C>s).
Throughout his career, Robert has been instrumental in driving success across critical areas including manufacturing operations, regulatory compliance, facility design and qualification, process development and validation, and strategic CAPEX/OPEX planning. He has played a pivotal role in supporting global expansion efforts for numerous organizations, offering expert guidance in CMC strategies, audits, and regulatory submissions, including BLA and MAA filings.
Robert has led major capital and operational projects, expertly managing contracts, procurement, and program delivery across international markets. His insights have been published in prominent industry textbooks and peer-reviewed technical journals. A recognized thought leader, he is a frequent speaker at industry seminars and technical conferences, and has served as a lecturer at universities and training institutions.
An active member of the Parenteral Drug Association (PDA) and the International Society for Pharmaceutical Engineering (ISPE) since 1990, Robert continues to shape the future of biopharmaceutical manufacturing through his leadership, technical contributions, and commitment to excellence.
The transition of large molecule drug substance manufacturing to a continuous operational model marks a significant evolution in biopharmaceutical production. This shift aims to increase manufacturing efficiency, enhance product quality, and reduce cost of goods. Achieving these goals requires overcoming several complex challenges including process control, sampling and testing, quality...
The often-overlooked function of chemistry, manufacturing, and controls (CMC) holds tremendous potential to reshape the landscape of drug development. By embracing innovation and rethinking traditional approaches, CMC has the rare opportunity to drive transformative changes that could significantly accelerate the journey from initial concept to a fully realized therapy. This offers the...
A growing segment of the advanced therapy medicinal product (ATMP) landscape, which includes gene therapies and cell-based treatments, relies heavily on viral vectors for efficient gene delivery. The increasing demand for these therapies requires a robust, scalable, and cost-effective manufacturing solution.
The 2022 Planning Committee is delighted to welcome attendance and registration for the fast-approaching ISPE Biotechnology Conference, taking place 28-30 June in Boston, Massachusetts and virtually.
This article revisits the concept of phased engineering, procurement, and construction (EPC) and updates it with risk-based considerations specifically regarding the commissioning, qualification, and validation (CQV) of general life-cycle principles for pharma and biotech projects. Enhancing the relationship between phases of a project, advanced planning, and more formal management of...
Continuous manufacturing has attracted significant interest over the past decade for small molecules formulated as drug products. The case for adopting continuous manufacturing platforms for manufacturing biologics (i.e., large proteins or biologic products such as vaccines) would, in principle, be even more justified for both quality and business gains. This article briefly reviews continuous...