SimoTech provides manufacturing automation and IT systems engineering, project management, and validation services. We partner with life sciences companies to design, build, operate, and optimise critical process automation systems that deliver fast track project delivery, operational efficiency, improve manufacturing agility and achieve regulatory compliance.
Why SimoTechWhat 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' life-changing supply of products to patients. In return, there is excellent salary, career progression, educational support and much more.
SimoTech has an exciting new opportunity for an experienced Automation Commissioning Engineer to join our client's site execution team. In this role, you will be essential to our client's successful commissioning and qualification execution of a new manufacturing facility in their East Cork pharmaceutical campus.
The ideal candidate will have previous site commissioning experience on life science manufacturing automation projects, along with hands-on expertise in working with Rockwell PLCs, and related hardware and applications. In this pivotal role, you will drive the successful delivery, commissioning, and qualification of advanced Process Control Systems (PCS) and Building Management Systems (BMS) for a global leader in the pharmaceutical industry.
Key ResponsibilitiesCoordinate and facilitate smooth interactions between System Integrators, Construction Management, and Equipment C&Q groups to ensure alignment and effective communication.Review and approve SAT and CSV documentation created by System Integrators, ensuring all deliverables meet stringent quality standards and regulatory requirements.Proactively manage and document system changes issued by the System Integrators, providing clear justifications and ensuring changes are thoroughly assessed and approved before implementation.Actively participate in daily standup meetings with CM and C&Q teams to discuss progress, address challenges, and align on priorities to maintain project momentum.Develop and maintain detailed weekly work plans in collaboration with System Integrators to ensure all tasks are scheduled effectively and resource allocation is optimised.Compile and present comprehensive status reports for automation systems, highlighting key milestones, progress, and any issues requiring attention.Provide expert troubleshooting support to resolve system issues promptly, minimising project disruptions and ensuring smooth project execution.Create CSV documentation where necessary to bridge gaps, ensuring complete validation coverage.Oversee the closure of automation system issues that impact C&Q, ensuring all issues are addressed and resolved efficiently.Facilitate the seamless handover of fully validated systems to the client team, ensuring all documentation and training are completed to the client's satisfaction.QualificationsBachelor's degree in engineering, computer science, or a related field.More than 6 years of relevant experience in automation and CSV in a pharmaceutical or biopharmaceutical manufacturing environment.Proven experience preferred with Rockwell Control Logix PLC and Archestra SCADA systems.Strong knowledge of cGMP and CSV guidelines.Excellent communication and presentation skills, with the ability to work effectively with diverse, multi-disciplined groups.Good Electrical & Instrumentation knowledge is an advantage.What SimoTech Can OfferRole 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 multi-disciplined environment.Opportunity to work with large corporate clients on exciting capital projects.
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