Randstad · 1 day ago
Senior Project Manager
Randstad is partnering with a top Biopharmaceutical company that is transforming the pharmaceutical industry through R&D-driven market leadership. The Senior Project Manager will play a key role in supporting site projects, ensuring timely supply of products and value to shareholders while applying project management methodologies and leading cross-functional teams.
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Responsibilities
As a part of the PMO you will be accountable to ensure adherence of the company’s PMM by all PMs on site, support and maintain the Takeda Project Portfolio Life Cycle Management (LCM) system and be an expert in Project Management at the site
Use project management tools to collect data to monitor & report on the progress of projects in the Portfolio and for intervention and problem solving with project teams
Review phase gate request deliverables for project phase completion and ensure teams focus on improving project management product quality
Provide training, coaching and support to project stakeholders (project team members, sponsors and steering committee members) in project and portfolio management best practices, business processes, methodology and tools
Continuously improve site Project Management practices & performance based on lessons learned and relevant KPIs
Support the deployment of strategy into the organization by helping facilitate the connection between the execution of the project portfolio and strategic programs
Lead cross-functional project teams and ensure project deliverables through all project phases (initiate through track) by managing project documentation, resources, costs, labor, purchases, invoice reconciliation, scheduling, budget, risk, communications, Environmental Health & Safety (EHS), quality compliance and maintain scope. Ensure projects are implemented within stated goals and timelines
Provide input to the project prioritization process and participate in other key strategic business portfolio processes to ensure proper prioritization and funding in support of site objectives
Adjust work plans, as appropriate, to meet changing needs and requirements
Responsible for making or escalating decisions for potential or actual impacts to successful implementation and closure of the project
Anticipate and positively resolve conflict situations, anticipate and eliminate or minimize barriers to progress, and implement mitigation for risks/issues
Clarify project requirements to meet stakeholder expectations
Manage expectations and communicate project status and escalations with project sponsor, senior management, and other internal and external stakeholders
Work under minimal supervision, independently planning and prioritizing work
May perform other duties as assigned
Qualification
Required
Ability to manage multiple projects and priorities at a time
Demonstrated experience applying project management methodologies
Experience supporting and leading projects in pharmaceutical/biotechnology regulated manufacturing environment
Proficient in relevant and current office equipment, tools, and software
Orientation to detail, business acumen, ethical and timely decision making
Possess a broad knowledge of business operations (principles, practices and procedures)
Strong communication and facilitation skills at all levels of the organization
Sense of urgency, flexibility, and accountability
Influences and drives change and supports others in the change management process
Ability to understand and translate business needs in defining solution requirements
Demonstrated leadership in leading teams of indirect reports
Ability to influence and think strategically
Must have uncompromising dedication to quality
Knowledge of regulated industries (GxP, FDA, ISPE, GAMP, ASTM E2500 standards/guidelines)
Software knowledge: Proficiency in Microsoft Applications including Outlook, Microsoft Project, PowerPoint, Teams, and PowerBI. Ariba, Veeva, SAP, and Trackwise is a plus
Minimum of 10 years of project management experience required leading complex cross-functional and technical projects (Process, equipment, commissioning and validation of systems, infrastructure, facilities, utilities, IT equipment, Digital)
Minimum of 5 years managing projects in the Pharmaceutical, Biotech (cGMP) industry
Preferred
Bachelor's degree in science, engineering, or related technical field preferred
PMP® certification preferred; Lean/Six Sigma certification preferred
Company
Randstad
Randstad is the world’s largest talent company and a partner of choice to clients.
H1B Sponsorship
Randstad has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2023 (754)
2022 (776)
2021 (1143)
2020 (1749)
Funding
Current Stage
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