Senior Biotech Operations Project Engineer - Dun Laoghaire, DublinOffice/Project Location:Dun Laoghaire, DublinEmployment Type: ContractWork Location: Site Based / HybridPay: €45 - €57 per hourExperience: 5+ yearsVisa: EU passport or Stamp 4 visa requiredSenior Biotech Operations Project Engineer - Dun Laoghaire, DublinOur client is a leading international Biotechnology company with a state of the art aseptic manufacturing facility in Dun Laoghaire, South Dublin.
The plant is one of the most dynamic in Ireland and is currently undergoing rapid expansion and capital investment.
This is an excellent opportunity to get experience into Ireland's leading aseptic manufacturing plant.The Project Engineer – New Syringe and AVI Lines Operations Readiness will report to the Operational Readiness Programme Lead within the Operations Function.
They will be responsible for providing project management and engineering support for projects in the Operations Readiness Programme for the new syringe and AVI lines.
You will have five to eight years of experience within the pharmaceutical or biotech industry and will have demonstrated project management skills.Experience in a project engineering and management role in a pharmaceutical or biotech manufacturing facility engaging with site SMEs and managers along with global functions.The ability to influence and lead cross functional teams to deliver their projects that ensure a smooth start-up of the new vial filling line.The ability to work independently and identify risks and mitigation pathways to ensure project delivery.A passion for continuous improvement applied to project management.Arrange agreement among the project team, customers, and management on the goals of the project.Work with workstream leads to develop and maintain the Project schedule/plan that aligns with the overall goals of the Programme.Effectively communicate with everyone involved in the project.Have a controlled scope in place, which 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.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.
RequirementsTechnical Degree and/or Masters' or equivalent Experience in a Life Science / Pharmaceutical / Biotechnology EnvironmentPreferred Experience: Project Engineering & Management, Aseptic Filling Line Operations, MES/EMBR, Validation, Greenfield / Brownfield start up.Systems / Equipment: MS Office, MS Project, MS PowerPoint, and MS Visio, Change Control & Document Management SystemsPreferred Requirements: SmartsheetHigh Energy and CommitmentAbility to work independently.Comfortable leading across multiple stakeholders & multinational teamsStrong ability to influence and affect change.Capable of resolving issues of conflict effectivelyStrong communicatorA proven track record 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 SolvingProvides leadership, guidance, and advice in own field of project management.Knowledge or experience with MES and EMBR projectsKnowledge or experience with validation of Aseptic Filling LinesPackageContract role - Hourly rate €45 - €57 per hourMinimum 12 month contract with the possibility of an extension.
