Automation Project Manager
- England, South West
- Contract
- CAPEX Projects
This vacancy has now expired
How would you like the opportunity to work with in one of the largest biopharmaceutical projects in the country? If yes, then this is the assignment for you!
Our client is currently seeking the skills of Automation Project Manager to join their team. Our client develops and delivers life changing medicines to millions of people globally and as part of their growth. With their Drug Substance (DS) manufacturing network growing rapidly, they are committed to growing their portfolio of commercial biologics products supplied worldwide – and this is your opportunity to be involved!
Responsibilities and Requirements:
- Process Automation System Architecture IFD
- Setting and agreeing the Automation Design Philosophy, in alignment with the Automation and IT strategies, technical standards and guidelines and local realties and expectations.
- Setting and agreeing the automation parts of the project deliverable list, including the Automation and IT RACI
- Lead the Automation User Requirements in alignment with relevant standards and guidelines.
- Supporting the Project Manager, Technical Project Manager, Work Package Owners, other SMEs with interpretation of the agreed Automation Design Philosophy and User Requirements.
- Supporting the Design Contractor(s) and Vendor(s) with translation of the agreed Automation Design Philosophy and User Requirements into Engineering deliverables.
- Establishing the resource estimates for the part of the automation delivery through all CPDP stages.
- Contribute to the technical assessment of critical equipment suppliers/contractors and provide selection recommendation.
- Work with Design Contractor/vendor to develop the design, translating technical requirements into Engineering deliverables.
- Provide design assurance overview and technical feedback throughout the project to ensure ongoing technical alignment and identification of value engineering opportunities:
- Produce regular Design Assurance Reports within their area of responsibility.
- Engage in the execution of design reviews.
- Ensure key SHE and GMP compliance requirements are reflected in the design deliverables.
If this role is of interest to you, please apply now!
#LI-AS3
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 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
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