The Pharmaceutical Development Program Manager (PDPM) is part of the Discovery, Product Development & Supply (DPDS) organization, responsible for delivering program outcomes for pharmaceutical development and lifecycle management programs within CMC and Preclinical Sciences & Translational Safety areas.
Locations (5)
Belgium, Belgium
Malvern, Pennsylvania, United States
Raritan, New Jersey, United States
Spring House, Pennsylvania, United States
Titusville, New Jersey, United States
Compensation
The anticipated base range for this position is $120,000.00 - $207,000.00
Responsibilities
Provide insights into project timelines and resources, exhibit proactive risk and issue management, and enhances asset value for pharmaceutical development and lifecycle management programs.
Drive strategic decisions and achieve key deliverables for the CMC team, PSTS team, and Project Management Team (PMT), based on available data, assumptions, scenario development and critical path analysis.
Provide expert advice on seamlessly implementing the development plan in line with key decision points and risk mitigation and avoidance activities.
Represent CMC and PSTS in PMTs to contribute to cross-functional planning, budgeting, and risk management, and act as key partner towards finance.
Participate in initiatives for continuous improvement and simplification across the PDPM role to provide project management support in a more efficient and effective manner.
Requirements
Bachelor's degree in a scientific field
Nice to have: project management in a matrix organization
The Pharmaceutical Development Program Manager (PDPM) is part of the Discovery, Product Development & Supply (DPDS) organization responsible for delivering program outcomes in Chemistry, Manufacturing, and Controls (CMC) and Preclinical Sciences & Translational Safety (PSTS) areas.
Seeking an experienced Director, Program Management Office (PMO) to establish and lead the PMO for Fluorescence Imaging (FI). This leader will build the program and project management organization, including its team, operating model, governance, tools, and reporting capabilities to support an expanding drug development portfolio.
Responsibilities
Establish and lead the FI PMO from inception, defining its charter, organizational structure, services, governance model, standards, and phased implementation plan
Assess portfolio needs and resource capacity; develop staffing plans and recruit, hire, coach, and manage program and project management personnel
Create or oversee development of scalable PMO infrastructure, including integrated program plans, portfolio schedules, dashboards, reporting tools, and performance metrics
Design and implement program governance, including leadership reviews, decision rights, escalation pathways, meeting structures, and risk, issue, action, and decision management
Direct program and project management activities across FI programs, ensuring alignment of CMC, Clinical, Regulatory, Nonclinical, Quality, and commercial-readiness plans
Requirements
Bachelor’s degree in life sciences
pharmaceutical sciences
related field
MBA
Nice to have: Project Management Professional (PMP) certification
The Associate Director of Global Clinical Supply Chain is responsible for the successful execution of supply chain management for clinical trials, providing triage support for rapid start-up of CDMOs and CROs, and ensuring continuous supply of Investigational Medicinal Product (IMP).
Compensation
Salary range for posting: $170,000—$200,000 USD
Responsibilities
Managing and executing overall Project Delivery through coordination of CMC efforts assigned to the entire project team (CMC, Supply Chain, Legal, Procurement, Regulatory, Clinical Development, and Clinical Operations).
Provides recommendations on packaging design, distribution and blinding strategy.
Plans and manages execution of initial supplies and resupplies for assigned studies.
Designs and implements plans to supply study drug to complex global clinical trials using sound supply chain techniques.
Develops and executes inventory management plans for clinical sites and depots to ensure treatment availability for every patient visit.
Requirements
Bachelor's degree in science, engineering, or another relevant field
Support the development and successful performance of the CMC regulatory strategy for the innovative pipeline of Cell & Gene Therapies.
Locations (3)
Santa Monica, California, United States
Gaithersburg, Maryland, United States
Boston, Massachusetts, United States
Compensation
The annual base pay (or hourly rate of compensation) for this position ranges from $135,624.80 - $203,437.20 USD Annual. Hourly and salaried non-exempt employees will also be paid overtime pay when working qualifying overtime hours. Base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience. In addition, our positions offer a short-term incentive bonus opportunity; eligibility to participate in our equity-based long-term incentive program (salaried roles), to receive a retirement contribution (hourly roles), and commission payment eligibility (sales roles).
Responsibilities
Interpret global regulations and guidance to identify risks and provide input for guidance to cross functional product teams.
Principal Scientist, Group Leader, Upstream Process Development
Lead scientists and engineers developing robust, scalable upstream processes and technologies for a diverse biologics portfolio, providing scientific, technical, and people leadership across cell culture and bioreactor development.
Compensation
The annual base salary for this position ranges from $106,000.00 to $176,600.00. In addition, this position is eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 15.0% of the base salary and eligibility to participate in our share based long term incentive program.
Responsibilities
Leads an upstream process development group with accountability for people leadership, technical strategy, portfolio delivery, innovation, and technology transfer.
Influences project teams and partner functions and advances capabilities within the group and discipline.
Lead and develop a team of scientists and engineers delivering upstream processes and technologies across multiple biologic development programs.
Establish priorities, allocate resources, and provide scientific direction to meet project and portfolio objectives; coach and develop colleagues while fostering an inclusive, collaborative, and high-performing environment.
Lead the design, optimization, scale-up, characterization, and transfer of upstream processes using strong biological and engineering fundamentals, high-throughput experimentation, automation, advanced sensing, modeling, and data-rich experimental approaches.
Requirements
Ph.D. in Chemical Engineering, Biochemical Engineering, Biotechnology, Microbiology, Cell Biology, Biochemistry, or a related field
Act as the US Regional technical liaison for gene and cell therapy product line, providing scientific leadership, product knowledge stewardship, and technical support to customers.
Compensation
The base salary range is $95,000 - $115,000 and is dependent upon experience level.
Responsibilities
Act as US Regional technical liaison for gene and cell therapy product line
Assist local account managers by attending technical calls, site visits and instrument demos
Create and optimize end-to-end CI workflow protocols
Provide expertise on regulatory compliance for GMP workflow
Liaise and manage custom projects with R&D and production
The anticipated base pay for for position is : $120,000.00 - $207,000.00
Responsibilities
Provide insights into project timelines and resources, exhibit proactive risk and issue management, and enhances asset value for pharmaceutical development and lifecycle management programs.
Drive strategic decisions and achieve key deliverables for the CMC team, PSTS team, and Project Management Team (PMT).
Provide expert advice on seamlessly implementing the development plan in line with key decision points and risk mitigation and avoidance activities.
Represent CMC and PSTS in PMTs to contribute to cross-functional planning, budgeting, and risk management, and act as key partner towards finance.
Participate in initiatives for continuous improvement and simplification across the PDPM role.
Requirements
Bachelor's degree in a scientific field
Advanced degree preferred
Nice to have: PMP (Project Management Professional certification)
Associate Director, Global Clinical Supply ChainNewIMVT Corporation · Remote, US
Associate Director, CMC Regulatory Affairs (Cell & Gene Therapies)AstraZeneca · Santa Monica, US+3 more
Field Application ScientistGenScript/ProBio · US