Senior Project Manager – Process DevelopmentIndustry: Pharma/Biotech/Clinical ResearchWork Experience: 5+ yearsCity: DublinState/Province: DublinCountry: IrelandJob DescriptionAbout PSC Biotech:
PSC Biotech is a leading Biotech Consultancy firm founded in 1996, headquartered in Pomona, California, USA, with global operations in Ireland, India, Singapore, Australia, and the US, serving 350 clients in more than 23 countries worldwide. We provide cloud-based software solutions for Quality Management and Regulatory Inspections, pharmaceuticals contract manufacturing professionals, and metrology services to our clients.
Senior Project Manager – Process Development Overview: The Snr Project Manager – Process Development will report to the Sr. Manager Process Development in the Portfolio Management and Delivery (PMD) group and will be responsible for managing new product introduction and lifecycle management projects for drug product (DP) and finished drug products (FDP). The successful candidate will have at least five to eight years of experience within the pharmaceutical or biotech industry and will have demonstrated project management skills.
RequirementsThe ideal candidate will have: Experience in a leadership role in a pharmaceutical or biotech manufacturing facility that engages with site SMEs and managers, and global functions.The ability to influence and lead cross-functional teams to ensure the smooth introduction of new products and the health of existing products.The ability to work independently and identify risks and mitigation pathways for new and existing products.A passion for continuous improvement applied to product and program leadership.Scope of Role: Arrange agreement among the project team, customers, and management on the goals of the project.Develop and maintain the project schedule/plan that addresses quality, objective, scope, cost, schedule, resources, and responsibilities to deliver the project and measure progress against schedule and budget.Effectively communicate with everyone involved in the project.Have a controlled scope in place that is understood by all stakeholders and maintained throughout completion of the project.Execute prudent risk and issue management.Maintain Actions/Risk and Decision logs.Generate and own the GMP change control.Motivate, support, and direct project team members to deliver on project plan.Lead team meetings and cross-functional collaboration.Work with resource managers from across the organization to effectively obtain and allocate resources to complete programs and projects on time.Compliance Related Tasks: Always ensure compliance to cGMP.Ensure safety & compliance standards are maintained to the highest standards.Ensure financial compliance in line with Business & Financial guidance.Support a culture of personal responsibility within reporting structure.Skills & Knowledge: High energy and commitment.Ability to work independently.Comfortable leading across multiple stakeholders & multinational teams.Strong ability to influence and affect change.Capable of resolving issues of conflict effectively.A proven track record in the ability to transfer goals and objectives into measurable plans.Ability to identify gaps/risks and put appropriate remediation plans in place.Uses strong relationships to identify requirements and potential opportunities.Employs project management techniques and problem-solving.Provides leadership, guidance, and advice in own field of project management.Qualifications and Experience: Technical Degree and/or Masters' or equivalent.5-8 years of experience (including a minimum of 3 years as Project Manager) in a Life Science / Pharmaceutical / Biotechnology Environment.Systems / Equipment: Smartsheet, MS Office, MS Project, MS PowerPoint, and MS Visio.
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