Summary:
A Project Manager (Drug Product Process Development) is required for a biopharmaceutical company in South Dublin. The incumbent will support a batch size increase project onsite. This is a hybrid role, that will require the incumbent to be on site 3 days per week.
Responsibilities: Arrange agreement among the project team, customers, and management on the goals of the project. Develops and maintains 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. Maintains Actions/Risk and Decision logs. Generates and owns the GMP change control. Motivate, support and direct project team members to deliver on project plan. Leads Team meetings and cross functional collaboration. Works with resource managers from across the organisation to effectively obtain and allocate resources to complete programs and projects on time. Always ensure compliance to cGMP. Ensure safety & compliance standards are maintained to the highest standards. Qualifications & Experience: Technical Degree and/or Masters' or equivalent. 5-8 years of experience (including min of 3yrs as Project Manager) in a Life Science / Pharmaceutical / Biotechnology Environment. Experience in a leadership role in a pharmaceutical or biotech manufacturing facility that engages with site SMEs and managers, and global functions. Provides leadership, guidance, and advice in own field of project management. Smartsheet, MS Office, MS Project, MS PowerPoint and MS Visio. Experience with TrackWise Change Control & Document Management Systems.
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