Why SimoTech
What is it like to work at SimoTech With a strong collaborative teamwork culture based on respect trust and excellence we play a critical partnering role to our clients lifechanging supply of products to patients. In return there is excellent salary benefits career progression educational support and much more.
VPE Automation Engineer 1552
SimoTech require a VPE Automation Engineer for a large multinational client based in Dublin. The ideal candidate will have a minimum of 5 years Automation experience in the biotechnology pharmaceutical or life sciences industries.
The successful candidate will be primarily site based responsible for implementing the full project lifecycle activities associated with Vendor Package Equipment (VPE) on a large biopharmaceutical site.
Key Responsibilities
- Lead and contribute to automation projects focused on longrange preventative maintenance obsolescence remediation new technology integration and plant modernisation/expansion.
- Ensure all automation and control system changes follow formal change management processes maintaining compliance with GMP and site engineering standards.
- Ensure consistency and standardisation across automation deliverables including requirements functional specifications and control strategies.
- Provide technical input review and approval of functional requirements and design specifications.
- Assist in defining developing and modifying software components as required to support system enhancements and operational improvements.
- Act as a key technical liaison by responding to systems integrator queries ensuring alignment with project goals and site standards.
- Support the development and of software testing strategies ensuring robust validation and compliance with regulatory requirements.
- Identify and assess remediation needs for process control systems to enhance system reliability and performance.
- Play a critical role in site integration commissioning and qualification of VPE systems to ensure seamless upgrade and deployment.
- Proactively track and manage issues in the issue tracker ensuring timely resolution and minimal impact on project timelines.
- Maintain clear and consistent communication with the Automation Manager providing regular updates on progress challenges and resource requirements.
Qualifications
- Bachelor s degree in Engineering Computer Science or related disciplines.
- 5 years working experience in Biopharmaceutical or Pharmaceutical engineering operations or manufacturing.
- 5 years experience in PLC/SCADA (Siemens & Rockwell technologies automation design configuration testing and qualification.
- Knowledge of GMPs regulatory requirements and computer system validation.
- Role provides a high degree of autonomy to allow the successful candidate to reach their full potential.
- Develop new skills and enhance technical ability by working with innovative technologies in a multidisciplined environment.
- Opportunity to work with large corporate client on exciting projects.