Pamela Wright Email & Phone Number

Tarrytown, New York, Us

Responsible for establishing and leading a team of 200 world-class scientists and engineers in a new 27,000 square foot state-of-the-art laboratory. Scope encompasses Upstream, Downstream, and Process Characterization and Controls to support regulatory filings, process investigations and process optimization of Regeneron’s clinical and commercial products. Established the Process Sciences New Modalities team to focus on technical support and process characterization of AAV, CAR T, ADC, and synthetic chemistry pipeline products.

Lawrence Township, Nj, Us

Designed and built a world-class CAR T Manufacturing Organization to manufacture 2 commercially licensed CAR T products: Abecma and Breyanzi. Responsible for recruiting and developing top talent, and providing leadership and oversight of commercial operations to meet world demand for both CAR T products at the BMS Summit NJ facility.

Parsippany, New Jersey, Us

Responsible for all GMP manufacture and supply chain operations to supply Anthim® in support of USG Procurement Contracts. Responsibilities include oversight, coordination, and management of 15 CMOs for bulk drug substance, drug product, analytical development & QC release testing, stability studies, packaging, GMP inventory control and cold chain shipping logistics.

Parsippany, New Jersey, Us

Responsible for oversight of GMP Manufacturing Campaigns in support of Process Transfer, Scale-Up, Validation and licensure of Anthim® (obiltoxaximab), a monoclonal antibody used as an anthrax anti-toxin developed under a $250 MM contract with BARDA.

Cambridge, Cambridgeshire, Gb

Responsible for aseptic filling, packaging and shipping operations for MedImmune Vaccines during H1N1 Pandemic. Provided leadership and direction for aseptic filling of H1N1 and FluMist® vaccines including Formulation and Aseptic Filling of vaccines, Supply Chain, and oversight of CMOs for buffer supply and commercial packaging of H1N1 and FluMist®.

Toronto, Ontario, Ca

Member of Site Leadership Team and BioCork Project Steering Committee, responsible for providing direction for $650M BioCork project facility design, start-up and GMP licensure. Responsible for building a new organization in Ireland, focused on technology transfer and manufacture of biologics and monoclonal antibodies.

Us

Responsible for Upstream Operations, including leadership for US and Ex-US licensure and commercial manufacture of REMICADE (infliximab).

Cambridge, Ma, Us

Responsible for clinical and commercial manufacture of biopharmaceutical products. Managed operating budgets and allocated headcount resources to support strategic plans.

Switzerland 🇨🇭 , Ch

Technology transfer and scale-up of new processes to large scale commercial manufacturing. Responsibilities also included directing new process development strategies and initiatives, and management of a Pilot Plant to support commercial operations.

Kenilworth, New Jersey, Us

Process development, scale-up and technology transfer of new fermentation, cell culture and purification processes for clinical and commercial production of antibiotics, biologics and monoclonal antibodies in Union N.J., Manati P.R., and Brinny Ireland.

Phd, Chemical & Biochemical Engineering

Ms, Chemical Engineering

Bs, Chemical Engineering