CUB Project Automation Area Lead
- North America, East Coast
- Contract
- CAPEX Projects
This is a fantastic opportunity for a CUB (Central Utilities Building) Project Automation Area Lead to join our major, global pharmaceutical client on their latest new-build project based in Ohio, this is a large-scale greenfield capital project and investing more than $1bn.
Responsibilities:
- Technical ownership for an area in a project
- Define the S88 software structure and list for the area
- Develop draft function design specifications for the area
- Work with system integrators to finalize the functional specifications
- Participate in P&ID and control strategy reviews
- Working closely with the Project Technical Lead and System Integrator to successfully deliver the project on schedule and budget
- Collaborate with Program technical offices to ensure the automation solution is aligned with the overall program automation philosophy and standards
- Ensure consistency of the automation deliverables in the area (requirements, functional specifications, control strategies, phases, and recipes, etc.)
- Assist in defining the software components that need to be created or modified
- Communicate progress, issues, and needs to automation technical lead for the project
- Provide input, review, and approve functional requirements and specifications
- Develop and partner with the selected System Integrator to create computer system validation deliverables (alarm rationalization, system overview, source code reviews, testing, etc.).
- Secure vendor documents for skidded equipment to integrate with validation deliverables.
- Responding to system integrator technical queries.
- Identify and analyse risks of technical nature particular to the area and planning responses.
- BS Engineering (or equivalent experience)
- Requires extensive working Automation experience in the Pharmaceutical Industry (preferable in API/bulk manufacturing)
- Previous Pharmaceutical Automation Large Project/Program experience/expertise
- Extensive experience in Allen-Bradley PLCs
- Previous experience in a Central Utilities Building
- Exceptional teamwork abilities
- Strong knowledge of GMP’s, regulatory requirements and computer system validation principles
- Excellent written and verbal communication skills for both technical and non-technical audiences
- Strong knowledge of GMP’s, regulatory requirements and computer system validation principles
- Excellent written and verbal communication skills for both technical and non-technical audiences
#LI-AN1
We have worked together with QCS Staffing for seven years now and have always received a professional service. QCS Staffing'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 QCS Staffing's people and their ability to deliver.
Global Pharmaceutical firm
I have always received a highly professional & personable service from the team at QCS Staffing. 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
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