Cmc Technical Senior Project Manager

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ppbSia /b 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.
/p pbSia Life Science and Healthcare Business Unit /b focuses on supporting Sia's clients in the life sciences and healthcare industries with strategic consulting, product development, and non-dilutive funding expertise.
/p pThis 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.
/p pOur subject matter experts help advance our clients' products and projects, supporting these companies – both large and small – to achieve organizational objectives and create tangible value for their stakeholders.
/p h3Job Description /h3 pThe bCMC (Chemistry, Manufacturing, and Controls) /b bTechnical Senior Project Manager /b provides operational management for CMC development and technical transfer projects.
/p pWorking in close partnership with the CMC Program Manager – who drives program-level strategy and communications – the Senior Project Manager leverages their technical and project management expertise to serve as the operational hub for CMC project teams, driving execution, communication, and accountability across process development, analytical, formulation, quality, and supply chain, as well as external partners.
/p pThis role blends technical understanding of biopharmaceutical CMC development disciplines with strong project management and coordination skills.
/p pCandidates are required to have biopharmaceutical industry experience through CMC technical roles with project management responsibility or through project management roles with a deep understanding of CMC development.
/p pbResponsibilities: /b /p pProviding consulting services for Sia's clients in the life sciences and healthcare industries, including but not limited to:



/p ul liProvide strategic oversight to maintain alignment of project milestones with day-to-day activities.
/li liResponsibility for content, quality, and distribution of project management deliverables (reports, dashboards, etc.) and routine updates (schedule, budget, risk), typically as the final reviewer.
/li liEstablish strong working relationships with leadership and project functional teams across all levels.
/li liServe as project spokesperson and facilitate communications with all internal and external stakeholders (meetings, reports, etc.).
/li liWork with cross-functional teams (CMC, Med. Affairs/Clinical, Nonclinical, Quality, Regulatory, Finance, Legal, Contracts Management, etc.) to drive project activities against scheduled timelines, approved scope, and approved budget.
/li liManage project financials, including vendor invoice review/approval, budget development, actuals tracking, maintenance of time?phased financial forecast, preparation of project financial reports for internal and external stakeholders.
/li liProactively manage strategic risks and issues, providing expertise in the identification and implementation of risk mitigation activities.
/li liDemonstrate and foster excellent teamwork, with the ability to navigate within multidisciplinary teams.
/li liBalance project demands to align/realign Budget, Quality, Timeline, and Scope, as needed.
/li liLead product development meetings, and ensure all Project Leaders, and/or subteam leaders, have all the information and support needed to implement the project.
/li liFocus on customer service, with agility and clear communication.
/li liAdhere to Siaquality standards regarding client deliverables.
/li /ul h3Qualifications /h3 pbMandatory qualifications: /b /p ul li8+ years of experience in the biopharmaceutical industry with a minimum of 5 years of project management experience.
/li liBS, MS, or PhD in a scientific or engineering discipline (e.g., Chemistry,



Biochemistry, Chemical or Biomedical Engineering, Pharmaceutical Sciences) /li liExperience working with CDMOs to support outsourced development and manufacturing activities, including oversight of deliverables and timelines.
/li liAbility to engage in technical and scientific discussions.
/li liStrong communication and interpersonal skills, with the ability to influence, collaborate, and build alignment across diverse technical and leadership teams.
/li liProficiency in Planisware and principles to plan, manage, and track multiple parallel projects in a complex, matrixed environment.
/li liFluent and articulate communication in English (written and spoken).
/li liExcellent written and oral communication, presentation, problem?solving, and negotiation skills with an emphasis on building consensus.
/li liAbility to work independently and in collaboration with others.
/li liFlexibility and ability to deal with ambiguity, and a sense of personal ownership of deliverables and results.
/li liWorks well with teams, often comprised of multiple disciplines.
/li liComprehensive understanding of CMC, including: ul liSmall molecule, biologics, or vaccine formulation, process development, analytical development, and GMP manufacturing across both early and late?stage development.
/li /ul /li liFormal project management training or certification (e.g., PMP).
/li liStrong understanding of product development lifecycle and pharmaceutical manufacturing operations.
/li liStrong understanding of cGXP guidelines and regulatory requirements.
/li /ul h3Additional Information /h3 pbWhy join the Sia Village?
/b /p pExcellence | Entrepreneurship | Innovation | Teamwork | Care Support | Employee Wellbeing /p pYour experience at Sia will be enriched by a(n): /p ul liSupport with achieving professional development goals through guidance and real?time feedback /li liContinuous learning development opportunities /li /ul pAll your information will be kept confidential according to EEO guidelines.
/p pSia Partners 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.
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Vedi l’offerta su Go Lavoro: golavoro.it/annuncio-lavoro/79fs43