Project Manager, Product Supply Chain

Overview
BioMarin 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, Cork
Summary 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.
Responsibilities
Project Planning and Execution: Developing detailed project plans, timelines, and resource allocation strategies
Budget & Schedule Management: Monitoring project costs, tracking spending, and ensuring projects stay within budget and on schedule
Risk Management: Identifying potential risks and developing mitigation strategies to minimize their impact
Team Leadership: Leading and motivating project teams, fostering collaboration, and ensuring effective communication
Stakeholder Management: Maintaining strong relationships with stakeholders, providing regular updates, and managing expectations
Compliance and Quality Assurance: Ensuring projects adhere to relevant regulations, standards, and quality requirements
Documentation and Reporting: Maintaining accurate project documentation and providing regular progress reports to stakeholders
Closeout and Evaluation: Overseeing project closeout activities, including final reports, financial reconciliation, and lessons learned
Scope
Developing project proposals and cost estimates
Creating and maintaining project schedules, including milestones and deadlines
Conducting regular project status meetings and providing updates to stakeholders
Managing project scope changes and ensuring they are properly documented and approved
Ensuring that all project deliverables meet the required quality standards
Managing project budgets and ensuring that spending is within the allocated limits
Managing project risks and developing mitigation plans
Leading and motivating project teams, including engineers, scientists, and other professionals
Communicating with stakeholders, including clients, senior management, and regulatory agencies
Education
Required: 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)
Experience
Project Management Expertise: 5-8 years of demonstrated experience in managing complex projects, preferably in the life sciences industry
Leadership Skills: Ability to lead and motivate teams, manage conflicts, and foster collaboration
Communication Skills: Excellent verbal and written communication skills, with the ability to effectively communicate with stakeholders at all levels
Analytical and Problem-Solving Skills: Ability to analyze complex situations, identify problems, and develop effective solutions
Technical Proficiency: Understanding of relevant technologies, processes, and regulations within the life sciences industry
Financial Acumen: Understanding of project budgeting, cost control, and financial reporting
Regulatory Knowledge: Familiarity with relevant regulations, such as GMP, FDA regulations, and other industry-specific standards
Approximately 15% travel
Contacts
TOPS 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 necessary
Note: 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 level
Mid-Senior level
Employment type
Full-time
Job function
Project Management and Information Technology
Industries
Biotechnology
Pharmaceutical Manufacturing
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