Sia is a next-generation, global management consulting group born digital, augmented by data, enhanced by creativity, and driven by responsibility. We partner with clients to resolve challenges and capitalize on opportunities. We believe that in today’s world of change and disruption, optimism is a force multiplier.
Sia’s Life Science and Healthcare Business Unit, Sia/LBG, focuses on supporting the life sciences and healthcare industries with strategic consulting, product development and non-dilutive funding expertise. This consulting division works with healthcare organizations, pharmaceutical & biotech companies, CROs, academia, medical device/diagnostic companies, and non-governmental organizations (NGOs) alike to solve complex business, scientific, regulatory, technological and product development challenges. Our subject matter experts help advance our clients products and programs; supporting these companies - both large and small - to achieve organizational objectives and create tangible value for their stakeholders.
Why join the Sia Village?
Excellence | Entrepreneurship | Innovation | Teamwork | Care & Support | Employee Wellbeing
These are the six core values that guide all our actions.
Your experience at Sia will be enriched by a(n):
Entrepreneurial journey
Support with achieving professional development goals through guidance and real-time feedback
Continuous learning & development opportunities
The Technical Project Manager provides day-to-day operational management for CMC development programs. Working in close partnership with the CMC Program Leader who drives program strategy, the project manager leverages their technical and project management expertise to serve as the operational hub for CMC program teams, driving execution, communication, and accountability across process development, analytical, formulation, quality, supply chain, and external partners.
This role blends technical understanding of biopharmaceutical CMC development disciplines with strong project management and coordination skills. Candidates are required to have biopharmaceutical industry experience through CMC technical roles with project management responsibility or through program management roles with deep understanding of CMC development.
Responsibilities
Project Operations & Execution
Lead day-to-day operational management of CMC development activities in an outsourced environment.
Apply technical judgment to build robust plans, anticipate risks, manage deviations, and respond to unforeseen challenges.
Build integrated CMC project plans, maintain, and track timelines, dependencies, and deliverables across CMC functions.
Ensure plans and timelines are executed as agreed.
Monitor progress against milestones, identify critical path activities, and proactively escalate issues.
Coordinate execution across internal technical teams and external partners (e.g., CDMO).
Risk & Issue Management
Support identification, tracking, and communication of CMC program risks (technical, regulatory, and supply-related).
Maintain risk registers, contingency plans, and decision logs.
Support the Program Leader in evaluating alternative scenarios and recommending operational adjustments.
Communication & Stakeholder Management
Manage day-to-day communication with internal stakeholders, leadership, and external partners.
Facilitate information flow between CMC teams and the Program Leader to ensure alignment and transparency.
Leverage technical background to help craft effective communications around complex CMC plans or issue resolution.
Prepare & maintain project dashboards, timelines, and progress reports for governance and program reviews.
Organize and facilitate CMC team meetings, including agendas, minutes, action tracking and documentation.
Budget & External Partner Management
Support contract-related activities, including statements of work, change orders, and purchase orders.
Track CMC and CDMO budgets, invoices, and spend in alignment with approved financial plans.
Coordinate with finance, legal, and procurement to support external sourcing activities.
Operational Excellence
Apply project management best practices to improve efficiency, consistency, and visibility of CMC execution.
Maintain and continuously improve planning tools, tracking systems, templates, and communication processes.
Partner with the CMC Program Leader and functional leads to strengthen CMC project planning and governance.
Mandatory qualifications
8-10 years of experience in the biopharmaceutical industry
Direct involvement in biopharmaceutical CMC development programs
As a designated project manager or in a technical role with significant project management responsibilities.
BS, MS, or PhD in a scientific or engineering discipline
E.g., Chemistry, Biochemistry, Chemical or Biomedical Engineering, Pharmaceutical Sciences
Experience working with CDMOs/CROs to support outsourced development and manufacturing activities, including oversight of deliverables and timelines.
Ability to engage in technical and scientific discussions.
Strong communication and interpersonal skills, with the ability to influence, collaborate, and build alignment across diverse technical and leadership teams.
Proficiency in project management tools (e.g., MS Project, Smartsheet, Planisware) and principles to plan, manage, and track multiple parallel projects in a complex, matrixed environment.
Fluent and articulate communication in English (written and spoken)
Ideal candidates
Comprehensive understanding of CMC
Including small molecule, biologics, or vaccine formulation, process development, analytical development, and GMP manufacturing across both early and late-stage development.
Demonstrated ability to identify and manage risks, develop mitigation plans, and proactively address issues to maintain program momentum.
Formal project management training or certification (e.g., PMP)
Sia is an equal opportunity employer. All aspects of employment, including hiring, promotion, remuneration, or discipline, are based solely on performance, competence, conduct, or business needs.
