Automation Lead
- East Coast
- Contract
- Life Sciences
This vacancy has now expired
Do you want to work with an exciting company who are an established market leader within their unique and niche field? We have a fantastic opportunity for a Automation Lead with Automation Lead experience to drive the delivery of a large new capital invest project on an initial 12-month contract. As Automation Lead you will play a key role in the successful delivery of a new state of the art facility.
Automation Lead Responsibilities:
- Specific functions include the following:
- Lead the automation team to create proven automation solutions that are safe, sustainable, and reliable.
- Act as a safety champion both by safety in design and field safety execution during construction and commissioning activities.
- Provide input and review of all relevant specs and drawings for packaging/process/formulation/inspection systems on the projects Ensure Rockwell PLC code is deployed and integrated to the AES (Automation Execution System) for Batch Recipe Integration
- Lead the effort to integrate the Rockwell AES Platform for the entire facility. FTBatch, Rockwell SCADA, PlantPAx, eProcedure, MES, thin client, OSI Historian are critical
- Lead the effort to integrate the vendor packed systems to the AES for master data purposes – time sync, domain integration, data backup, OSI PI interfaces as well as interfaces from the PLC to the AES
- Work with the vendors to incorporate alarm integration, parameter integration, control integration, historian integration and reporting into the AES system
- Lead design for future interconnectivity for the network, domain, and data integration for the analytics packages
- Deploy AES and supporting systems for a dedicated virtual infrastructure for the AES with capacity to support virtualization of vendor systems or analytical systems
- Provide input and review of equipment selection and automation coordination. Including adherence of A/E and contractor partners in successfully implementing the automation execution strategy.
- Support Review of FATs, SATs, CQV and turnover packages
- Participate in design reviews and HAZOPs
- Education: Engineering Degree (BS or MS), from an Accredited Institution or equivalent experience
- Experience: Minimum 10 years related automation experience leading automation on projects
- Experience: Significant experience with automation design in a pharmaceutical environment including Rockwell automation, thin client, OSI PI, EMS, BMS, and others mentioned in the role section
- Experience: Managing sub-contracts
- Language Skills: Excellent English reading, writing, speaking and communication skills required
The candidate must have the rights to work in the location stated in the job advert.
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I have always received a highly professional & personable service from the team at Quanta. They listen carefully to the specific requirements of available roles and work tirelessly to supply a pool of potential candidates and make the hiring and contract renewal process an easy activity to manage.
Global Pharmaceutical firm
Once again can I via you recognise the superb support I was given before, during and after this short contract. The support, was as usual professional and every friendly.
QA Specialist
We have worked together with Quanta for seven years now and have always received a professional service. Quanta’s speciality certainly lies within their technical sourcing abilities and they have met our demanding requirements time and time again. Coupled with this are the integrity of Quanta’s people and their ability to deliver.
Global Pharmaceutical firm
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