Senior Project/Equipment Engineer Role
We are recruiting for a Senior Project/Equipment Engineer to join our team at a Pharmaceutical organization in Athlone.
This is an excellent opportunity for anyone looking to work with a leading multinational company that excels in its field.
About the Role
The Senior Project/Equipment Engineer will report to the Senior Manager for Strategic Engineering Projects and be responsible for scoping and executing technical projects supporting Drug Product manufacturing within various areas.
Key Responsibilities:
* Project management and execution of assigned projects, including project prioritization, resource management, status management, and external communication.
* Working with stakeholders to scope projects and ensure requirements are satisfied, from concept through design, construction, commissioning, and operation.
* Coordinating the introduction of new processes, equipment, and materials, including problem-solving and troubleshooting equipment issues prior to qualification & start-up.
* Development and implementation of maintenance programs and spare parts inventory optimization with the introduction of new equipment.
* Ability to translate strategic/emerging technology solutions into pragmatic executable plans.
* Development and management of change controls.
* Participation as a member of multidisciplinary site and multisite teams.
* Development of detailed specifications, engineering documents, protocols, and standard operating procedures.
* Collaboration within the Process Teams structure and contribution to Root Cause Investigations and Cross Functional Investigations.
* Collaboration with System Owners, Maintenance Supervisors & Technicians, Capital Project Engineers, and Vendors to perform equipment upgrades and/or retrofits.
* Performance of all tasks with due care and attention, ensuring compliance with Good Manufacturing Practices and company requirements, policies, and procedures.
* Safety support by complying with environmental health/safety practices, rules, and regulations.
* Possible travel to support project execution.
Requirements
* Bachelor's Degree in Engineering (Mechanical, Electrical, or Chemical) or Relevant Experience.
* Typically 3+ years of engineering experience, preferably in the biotechnology industry/aseptic pharmaceutical environment or Automated Inspection and/or Automated Device Assembly, Labelling, and Ancillary processes.
* Proven project management experience.
* Strong mechanical capability with hands-on experience in a technical role within a high-volume manufacturing environment.
* Demonstrated experience in a GDP Compliant environment.
This is a great opportunity for those interested in working with a leading pharmaceutical organization.