Senior Project Equipment Engineer
4 days ago
We're currently recruiting for an exciting opportunity with a Pharmaceutical organization based in Athlone. This is an excellent position for anyone who is looking to join a leading multinational who are one of the best at what they do.
The Senior Project / Equipment Engineer reports to the Senior Manager for Strategic Engineering Projects and is responsible for scoping and executing technical projects supporting Drug Product manufacturing within Formulation, Component Preparation, Vial/Syringe Filling, Lyophilisation, Device Assembly, Inspection, Labelling and Packaging areas. This includes qualification of new equipment and implementation of associated reliability and maintenance programs.
Key Responsibilities- Project management and execution of assigned projects including project prioritization, resources management, status management and external communication.
- Working with various stakeholders, to scope projects and ensure requirements are satisfied. Project input will NOTAG 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.
- Participate as a member of multidisciplinary site and multisite teams.
- Development of detailed specifications, engineering documents, protocols and standard operating procedures.
- Work in a collaborative manner within the Process Teams structure and contribute to Root Cause Investigations and Cross Functional Investigations.
- Work collaboratively with System Owners, Maintenance Supervisors & Technicians, Capital Project Engineers and Vendors to perform equipment upgrade and/or retrofits.
- Perform all tasks with due care and attention ensuring compliance with Good Manufacturing Practices and company requirements, policies and procedures.
- Support a safe working environment by complying with environmental health/safety practices, rules and regulations.
- Travel may be required to support execution of projects.
- Bachelor's Degree in Engineering (Mechanical, Electrical or Chemical) or Relevant Experience.
- Typically, 3+ years 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, is advantageous.
- Demonstrated experience in a GDP Compliant environment.
If interested in this posting please feel free to contact Seán McCarthy on +353 (0)87 798 8480 or sean.mccarthy@lifescience.ie for further information.
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