Project Manager, Product Supply Chain

OverviewBioMarin is a global biotechnology company that relentlessly pursues bold science to translate genetic discoveries into new medicines that advance the future of human health.BioMarin's Technical Operations group is responsible for creating our drugs for use in clinical trials and for scaling production of those drugs for the commercial market.These engineers, technicians, scientists and support staff build and maintain BioMarin's cutting-edge manufacturing processes and sites, provide quality assurance and quality control to ensure we meet regulatory standards, and procure the needed goods and services to support manufacturing and coordinating the worldwide movement of our drugs to patients.Position: Project Manager, Product Supply Chain |Location: Shanbally, Ringaskiddy, CorkSummary Description:Oversees and leads projects in support of early programs Product Supply Chain Teams and Commercial Value Chain Teams, ensuring they are completed on time, within budget, and to the required quality standards.This role involves planning, executing, and closing out projects, managing teams, and collaborating with various stakeholders.Key responsibilities include developing project plans, managing budgets and schedules, mitigating risks, and ensuring compliance with regulations.ResponsibilitiesProject Planning and Execution: Developing detailed project plans, timelines, and resource allocation strategiesBudget & Schedule Management: Monitoring project costs, tracking spending, and ensuring projects stay within budget and on scheduleRisk Management: Identifying potential risks and developing mitigation strategies to minimize their impactTeam Leadership: Leading and motivating project teams, fostering collaboration, and ensuring effective communicationStakeholder Management: Maintaining strong relationships with stakeholders, providing regular updates, and managing expectationsCompliance and Quality Assurance: Ensuring projects adhere to relevant regulations, standards, and quality requirementsDocumentation and Reporting: Maintaining accurate project documentation and providing regular progress reports to stakeholdersCloseout and Evaluation: Overseeing project closeout activities, including final reports, financial reconciliation, and lessons learnedScopeDeveloping project proposals and cost estimatesCreating and maintaining project schedules, including milestones and deadlinesConducting regular project status meetings and providing updates to stakeholdersManaging project scope changes and ensuring they are properly documented and approvedEnsuring that all project deliverables meet the required quality standardsManaging project budgets and ensuring that spending is within the allocated limitsManaging project risks and developing mitigation plansLeading and motivating project teams, including engineers, scientists, and other professionalsCommunicating with stakeholders, including clients, senior management, and regulatory agenciesEducationRequired: bachelor's degree in a relevant field (e.g., science, engineering, or project management)Preferred: A master's degree or relevant certifications (e.g., PMP)ExperienceProject Management Expertise: 5-8 years of demonstrated experience in managing complex projects, preferably in the life sciences industryLeadership Skills: Ability to lead and motivate teams, manage conflicts, and foster collaborationCommunication Skills: Excellent verbal and written communication skills, with the ability to effectively communicate with stakeholders at all levelsAnalytical and Problem-Solving Skills: Ability to analyze complex situations, identify problems, and develop effective solutionsTechnical Proficiency: Understanding of relevant technologies, processes, and regulations within the life sciences industryFinancial Acumen: Understanding of project budgeting, cost control, and financial reportingRegulatory Knowledge: Familiarity with relevant regulations, such as GMP, FDA regulations, and other industry-specific standardsApproximately 15% travelContactsTOPS and PSCT product teams, GSC Planning, Site SC and Operations, Regulatory, Commercial Ops., Master Data team, Logistics, Artwork / Packaging Operations, Quality, Finance and other functions as necessaryNote: This description is not intended to be all-inclusive, or a limitation of the duties of the position.It is intended to describe the general nature of the job that may include other duties as assumed or assigned.An Equal Opportunity Employer.All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability.Seniority levelMid-Senior levelEmployment typeFull-timeJob functionProject Management and Information TechnologyIndustriesBiotechnologyPharmaceutical ManufacturingReferrals increase your chances of 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