Project Manager, Product Supply Chain

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BioMarin Pharmaceutical Inc.

Site WebLinkedInTous les Emplois

1001 - 5000 employés

Fondée en 1997

🧬 Biotechnologie

💊 Pharmaceutique

💰 Post-IPO Debt en 2020-05

Biotechnology • Pharmaceuticals

BioMarin Pharmaceutical Inc. est une entreprise de biotechnologie mondiale de premier plan, dédiée à transformer les découvertes génétiques en médicaments innovants. Fondée en 1997, l'entreprise a développé huit produits commercialisés qui traitent des maladies génétiques et des troubles du stockage lysosomal mettant en jeu le pronostic vital, tels que l'achondroplasie et l'hémophilie A sévère. BioMarin investit fortement dans la recherche et le développement, avec un pipeline robuste de médicaments expérimentaux à divers stades d'essais cliniques. La mission de l'entreprise tourne autour de l'amélioration des soins aux patients en utilisant une expertise scientifique pour comprendre les causes sous-jacentes de ces conditions. BioMarin s'engage à l'inclusivité et à la défense des patients, en travaillant étroitement avec les communautés pour améliorer les soins et la qualité de vie des personnes atteintes de maladies rares.

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. • 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) is t required. • 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. • WORK ENVIRONMENT / PHYSICAL DEMANDS The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. The employee may frequently be required to sit and talk or hear. The employee is occasionally required to stand; walk; use hands and fingers, handle, or feel; reach with hands and arms; climb or balance; stoop, kneel, crouch, or crawl and taste or smell. The employee must occasionally lift and/or move up to 25 pounds. Specific vision abilities by this job include close vision, depth perception and ability to adjust focus. Approximately 15% travel EQUIPMENT Standard office desk equipment 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 SUPERVISOR RESPONSIBILITY There are no direct supervisory responsibilities with this job. CAREER DEVELOPMENT Refer to Responsibilities section 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. Equal Opportunity Employer/Veterans/Disabled 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.

🎯 Exigences

• 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) • 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