Program Manager
- Midlands (Ireland)
- Contract
- Compliance / Quality Assurance
With worldwide demand for their life-changing oncology treatment increasing; one of our global pharmaceutical clients is looking for a Program Manager to join their team to support multiple capital projects taking place onsite in Cork.
This is a fantastic opportunity to work on a state-of-the art fill-finish facility and the company’s first stand-alone vaccine and biologics plant outside the US.
Primary activities/responsibilities:
- Lead a strategic program and execute it in line with the PMO best practices.
- Ensure there is a strong safety culture and performance in the execution of projects.
- Ensure that the program delivers high-quality outcomes. This includes monitoring quality and taking action to address any quality issues.
- Oversee all activities associated with the Program to ensure the Program achieves it goals.
- Develop a comprehensive program plan and schedule that outlines the objectives, scope, timelines, budget, and resources required for the Program.
- Identify and manage risks associated with the Program. This includes developing a risk management plan, monitoring risks, and taking action to mitigate them.
- Monitor Program progress against the Program plan and schedule. This includes tracking milestones, identifying issues, and taking corrective action as necessary.
- Communicate with Program stakeholders, managing expectations, and addressing concerns.
- Responsible for the ongoing support of Project Managers in their delivery of projects within the Program, in line with schedule, scope, cost and resource requirements and constraints.
- Support the consistent use of PMO PPM digital tool (OnePMO) by the Project Managers and support PMO where necessary.
- As part of the PMO Portfolio Governance process, supports the analysis of Program data, identifying lessons learned and improvements.
- Monitor the Program against the objectives, identifying areas for improvement, and providing feedback to the PMO and Program team.
- Ensure highest Quality & Compliance standards. Participate and Comply with the Company’s Quality Management System.
Qualifications, Experience & Attributes:
- Relevant 3rd level qualification in Engineering, Business, or a related discipline.
- Qualification in project management such as PMP desirable.
- A minimum of eight to ten years in a project-related environment preferable Pharma.
- Strong knowledge of project and program management methodologies and industry best practice.
- Proficiency in MS Project scheduling tool required.
- Evidence of Continuous Professional Development essential.
- Proven track record in dealing with complex issues proactively and in a timely fashion and ability to achieve results within the set timeframe.
- Excellent communication skills and ability to work within a multi-disciplinary team with excellent people management and leadership skills.
The candidate must have the rights to work in the location stated in the job advert.
Please note, Quanta part of QCS Staffing does not sponsor Visa applications.
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Once again can I via you recognise the superb support I was given before, during and after this short contract. The support, was as usual professional and every friendly.
QA Specialist
We have worked together with Quanta for seven years now and have always received a professional service. Quanta’s speciality certainly lies within their technical sourcing abilities and they have met our demanding requirements time and time again. Coupled with this are the integrity of Quanta’s people and their ability to deliver.
Global Pharmaceutical firm
I have always received a highly professional & personable service from the team at Quanta. They listen carefully to the specific requirements of available roles and work tirelessly to supply a pool of potential candidates and make the hiring and contract renewal process an easy activity to manage.
Global Pharmaceutical firm
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