
Project Equipment Engineer
- Dublin
- Contract
- Full-time
- This is an excellent opportunity to join a world class manufacturing operation, with an outstanding track record of reliably delivering high-quality medicines to patients around the world suffering serious illnesses.
- There is a strong culture of continuous improvement and innovation within the company to strive for solutions that improve health outcomes and dramatically improve people’s lives.
- Our client is developing the capability to produce all its medicines in Dublin, helping to ensure continuity of supply of our medicines as they expand internationally.
- 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 span 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 contributes to Root Cause Investigations and Cross Functional Investigations.
- Works in a collaborative manner with the 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 practice, rules and regulations.
- Travel may be required to support execution of projects.
- Any other duties as assigned.
- 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.
- Experience in MS Office, MS Project, Change Control & Document Management Systems.
- Proven ability working cross functionally, delivering technical solutions and implementing improvements.
- Solid leadership skillset and experience working in a team environment, embracing an interdependent working culture that delivers results.
- Technical report writing and communication/presentation skills.
- Data driven decision maker.
- Ability to work to tight deadlines in a fast-moving environment.