Project Automation Area Lead
- North America, United States
- Contract
- CAPEX Projects
This is a fantastic opportunity for a 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 Parameter and Recipe Specification documents
- Responding to system integrator technical queries
- Identification of any remediation effort required on process control software
- Create items in the issue tracker as issues arise after the software acceptance
- Identify and analyze risks of technical nature particular to the area and planning responses
- Maintain compliance with training requirements
- BS Engineering (or equivalent experience)
- Extensive Automation experience in the Pharmaceutical Industry (preferable in API/bulk manufacturing)
- Previous Pharmaceutical Automation Large Project/Program experience/expertise
- Extensive experience in DeltaV Batch DCS
- Preferable, previous experience with Allen-Bradley PLCs
- 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
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
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
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
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