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Principal Engineer – Vial Filling

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Principal Engineer – Vial Filling

Ireland - Dun Laoghaire Apply Now
JOB ID: R-208044 LOCATION: Ireland - Dun Laoghaire WORK LOCATION TYPE: On Site DATE POSTED: Feb. 18, 2025 CATEGORY: Engineering

Reporting to the Engineering Snr. Manger, this person is accountable for leading a team supporting commercial manufacturing with a focus on Vial filling equipment. The position will support complex and challenging manufacturing initiatives.


Key Responsibilities:
•    Provide tactical as well as strategic management and leadership to provide operational support and project completion, mentoring, staff development, team productivity and efficient use of available resources. 
•    Planning support structures with internal/cross-functional teams for capital projects, goals and network initiatives execution. Providing input into department objectives and establishment of strategic direction within the F&E team. 
•    Lead the direction for vial filling unit operations for as it relates to the equipment; work together with the system owners to ensure both urgent day-to-day equipment reliability issues are resolved as well as longer term focus areas are planned for appropriately. 
•    Maintain and improve plant capability and equipment reliability in partnership with F&E and plant leadership and other technical staff in the network with a focus on “predict and prevent” systems failures and recurrence avoidance. Strategize asset lifecycle management and long-range plans for equipment maintenance. 
•    Work with diverse groups (Manufacturing, Quality, PD, Automation, IS, EHSS, Global Engineering) and drive new business processes to ensure continuous and sustained improvements. 
•    Translate business needs into engineering technology solutions. Lead analysis of alternatives and recommendations for technical/business proposals. 
•    Identify areas of potential improvement, conduct analyses, recommend solutions, sponsor improvement projects and implement. 
•    Ensure site readiness and compliance for internal audits, external agency audits, and partner audits. Ensure that all staff are adequately trained and follow all GMP standards and procedures.
•    Support Business Continuity Plans by identifying gaps and develop/implement solutions to close the gaps. 
•    Develop and adhere to department budgets and spend for operational and capital expenses. 
•    Be knowledgeable and current on compliance and regulatory aspects for operation and maintenance, equipment validation and support regulatory inspections and audits.
•    Support a safe working environment by complying with all pertinent environmental health/safety practice, rules and regulations.


Preferred Qualifications:
•    Bachelor’s Degree in Engineering (Mechanical, Electrical or Chemical) 
•    Manufacturing experience in biopharmaceutical Formulation/Fill/Finish
•    Solid leadership, technical writing, and communication/presentation skills 
•    Experience in change control, non-conformance, corrective and preventative actions, and validation practices
•    Experience in developing strategies for new product introduction and new technology deployment
•    Ability to translate strategic opportunities and emerging technology solutions into tangible pragmatic executable plans
•    Ability to influence the development of business area strategy and engineering/equipment strategy where appropriate
•    Ensure application of corporate blueprint and standards using business drivers to local business needs
•    Development and presentation of project plans to senior management
•    Day to day vendor management and contract negotiations with focus on equipment suppliers
•    Independent, self-motivated, organized, able to multi-task in project environments and skilled in communication and collaboration
•    Team player, prepared to work in and embrace a team-based culture that relies on collaboration for effective decision-making.

Travel at various times may be required to support execution of projects

Apply Now
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