GerTEK is an engineering consultancy company specialising in project management, talent solutions and commissioning qualification and validation services (CQV) to the life sciences and technology sectors. We partner with many of the world's largest life science & technology companies who entrust in us to deliver their most strategic and important projects.
Program Manager, Sligo
Objective
* Coordinate site project team to deliver Biological projects.
* Develop realistic cross functional implementation plans with input from above site and site functions (R&D, Engineering, Manufacturing, Quality, Regulatory, Commercial, Supply Chain, Finance, HR).
* Utilize the relevant PMO tools for project planning, monitoring and reporting.
* Set project milestones and report progress accordingly. Consider alternative approaches and take corrective actions as needed to ensure project milestones are achieved.
* Provide program management support for and guide the efforts of third-party organisations (vendors, suppliers, contractors, etc.) to enable achievement of shared milestones.
* Lead project teams to ensure efficient communication between resources.
* Engage with all stakeholders to ensure full alignment on priorities and proactively manage and report project risks.
* Work with cross functional teams to develop required change plans and raise/track change plans in the appropriate systems.
* Accountable for managing the project timeline and reporting any potential delay/risk on the critical path.
* Identify and implement opportunities that will improve the organization's ability to implement and manufacture quality products in a cost effective, compliant, and timely manner.
Other duties as assigned, such as facilitating and coordinating communication and actions between site resources and the global engineering team in relation to the delivery of equipment and the facilities required to support the NPI Program.
Supervision Received
* Operates in own environment which is largely self-managed but with supervision through the Site Leadership team and Business Excellence Manager.
* Goals are reviewed on a regular basis and formal performance reviews are carried out once per year.
Supervision Provided
* Have contacts with all levels of management at site and above site (Global functions) as per project requirements: R&D, Engineering, Manufacturing, Quality, Regulatory, Commercial, Supply Chain, Finance, HR.
Education:
Essential Requirements
* Degree in Engineering, Science, business, Project management or related discipline.
* PMI certification is desirable.
Desired Requirements
* Program Management experience.
* Ops experience in Sterile Manufacturing.
* Understanding of Engineering/Equipment/Validation processes used in a sterile environment.
* Previous experience in setting up new Bio processes/equipment/plants and/or NPI.
* Experience with One Vault/Soltracks system is an advantage.
Technical/Business Knowledge - Job Skills/Experience Required
* 5 years of diversified Pharma/Bio business experience: operations support, quality, supply chain, validations, capital and expense management, commercial product launches.
Benefits
* Highly competitive salaries/hourly rates.
* Career development.
* Mentorship programs.
* Hands-on training.
* Good working culture.
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