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Details
Project Scheduler
Reference: | AMC23381 | Location: |
Louth |
Qualification: | Degree | Experience: | See description |
Job Type: | Fixed Term Contract | Salary: | Not Disclosed |
May be suitable for:
Project Lead
Project Scheduler
12 month contact
On site - Louth
AMC23381
Project Scheduler - Biopharmaceutical Manufacturing
We are currently seeking an experienced Project Scheduler to develop and maintain a detailed, resource-mapped Site Integrated Schedule for a new biopharmaceutical manufacturing site. This role will combine multiple independent plans into a single portfolio plan and build new schedules for critical activities from capital projects to PPQ/Commercial supply.
Key Responsibilities:
- Drive the creation of the Site Portfolio Schedule (Microsoft Project).
- Transfer/Build existing project schedules in Microsoft Project, connecting to Primavera schedules where needed.
- Lead or participate in interactive scheduling workshops with various individuals and teams to further develop the schedule.
- Maintain the site portfolio schedule, align sub-project schedules, and issue progress metrics. Support site governance in mitigation plan tracking.
- Develop a close working relationship with the capital project scheduler to identify critical common milestones and workload peaks, ensuring a tightly integrated schedule.
- Monitor progress and provide timely updates showing impact on milestones.
- Identify mitigations for impending delays and risks.
- Provide regular updates to the project manager, leadership team, and site project management office using established reporting tools.
- 5-8 years' experience as a Project Scheduler in a pharmaceutical or biopharmaceutical environment, with at least one major project involving MES and MBR implementation.
- Proficiency in Primavera and Microsoft Project scheduling tools.
- Proficiency in Microsoft Excel, PowerPoint, Word, Outlook, and SharePoint.
- Excellent interpersonal and communication skills (written and verbal).
- Bachelor's/Master's degree in a relevant scientific or technical field.
- Project Management Professional (PMP) certification or similar.
- A self-starter who can proactively resolve issues.
- Able to multitask and work to tight deadlines.
- Results and performance-driven.
- Adaptable and flexible.
This is a chance to gain further experience across the extended project lifecycle, from start-up to PPQ batch completion on both capital and client projects within a strategic and high-profile biopharmaceutical initiative.
For more information or to apply contact Angela McCauley at Life Science Recruitment
Pharma Sales Scientific Manufacturing Executive IT Chemistry Allied Healthcare Engineering Life Science Supply Chain PhD Cork City Mayo Academic Diagnostics Quality Assurance Cork Limerick Project Manager Scientist Medical Device Validation Engineer Biopharmaceutical Pharmaceutical Product Development Engineer Laboratory Scientist Packaging Engineer Quality Engineering Connected Health Sales and Marketing Biotechnology Clinical Research Academic Sales and Marketing Supply Chain Medical Affairs Microbiology Quality Control Dublin
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Life Science Recruitment | Tel:+353 1 685 4848 | Fax: +353 (0)1 443 05 24 | Email: [email protected] | Copyright © 2021 Life Science Recruitment Ltd
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Life Science Recruitment | Tel:+353 1 685 4848 | Fax: +353 (0)1 443 05 24 | Email: [email protected] | Copyright © 2021 Life Science Recruitment Ltd
This site uses cookies. More information on cookies can be found in our Privacy Policy | Terms of Use | Registered as a private limited company. No: 445328
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