The Program/Project Manager is responsible for providing comprehensive project and support function scheduling and project management support to the company’s Manufacturing Facility based in Co. Dublin.
The Program/Project Manager must ensure that project objectives and milestones are effectively achieved and consistent with requirements to ensure compliance, safety and efficient project execution.
Core Duties and Responsibilities:
Development and maintenance of an integrated project schedule to include Engineering, Operations, Quality and Project activities, highlighting key milestones.
FDA Audit readiness
Capital Project Program
Continuous Improvement Projects
5-year strategic projects including enterprise production schedule, site development plan
Establish and effectively manage information management systems, develop reports, presentations, project updates, schedules and timeline updates and correspondence utilizing many different computerized systems.
Use standard systems including MS Word, MS Project, Excel, PowerPoint and industry/ company specific software for project management, document tracking, reporting, etc.
Maintain overall program schedule, review and communicate detailed critical path schedules.
Ensure co-ordination of detailed schedules highlighting resource and deliverables loading.
Provide effective administrative support to facilitate efficient project management. This may include tasks such as analyzing and reviewing data and compiling summary documents.
Format, write, deliver and review necessary documentation in line with the standard approval process, and facilitate others to do so.
Be a document system expert; this will include document review, approval and document system workflow expedition.
Support divisional activities through documentation generation, filing, tracking, auditing and maintenance of associated databases.
May be asked to perform other duties as required, particularly in support of critical manufacturing activities.
Minimum Qualifications and Experience:
Degree/Diploma level qualification in Project Management or Engineering
Minimum 10 years’ experience in the Pharmaceutical industry or a similar operating environment.
Experience in dealing with plant leadership level stakeholders
Scheduling systems: Primavera, MS Project planning experience.
Technical cGMP pharmaceutical knowledge and experience of project execution logic.
Proven application of various planning methodologies used on Facility Construction and Process Equipment development and integration projects.
Experience of working in professional service company.
Experience in planning activities within the confines of stringent EHS processes.
Experience of operating within a Computerized Maintenance Management System (CMMS).
Experience in the application of lean principles and structured problem-solving techniques.
Demonstrated ability to identify improvement initiatives.
An ability to work independently and as part of a team. The successful candidate will be able to organise their own work on a routine basis and requires minimal supervision.
Experience in working in cross-functional teams.
Competencies/Preferred Skills
Good interpersonal and communication skills.
Excellent documentation skills.
Thorough, diligent, rigorous attention to detail.
Collaborator with strong levels of engagement with individuals and team.
High level of delivery and work completion.
Enthusiastic, flexible, keen to develop.
Ability to manage ambiguity and change.
High levels of integrity and trustworthiness.
Ability to operate effectively with minimum supervision.
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