Description
Automation SME - Pharmaceuticals - 12-Month Contract
Opportunity
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 an Automation SME 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!
Scope
- Experience with Copa-Data Zenon installation.
- Work with key business users to convert project requirements into an automation strategy/requirements and technical solution.
- Define core Automation and IT integration requirements on projects into User Requirement Documents: communicating these requirements to vendors and ensuring that systems are specified and delivered in alignment with the automation strategy (contract management not part of this role).
- Provide design assurance reporting and technical feedback during capital project design - from concept through detailed design and equipment selection (Including where necessary, detailed design document reviews and sign off).
- Support Lead OT SME, Project Technical Manager, and Work Package Owners during all phases of project in technical issue management and governance to ensure a compliant technical solution to quality and safety.
- Involvement in C&Q testing and qualification activities (Including where necessary, document generation and test participation).
- Support the Work Package Owner to proactively plan the work ahead.
- Involvement in Assembly and Packaging equipment design documents, validation planning, hands-on FAT testing at EU based equipment vendors.
Experience
- Minimum of 5 years of experience in automation system engineering within the pharmaceutical industry.
- Proven experience in managing and executing automation C&Q projects in a global setting, particularly in China or Europe.
- Experience in the full lifecycle of delivering automation systems in a licensed GMP commercial facility (Including design, specification, procurement, installation, start-up, commissioning).
- Strong knowledge of automation systems including PLCs (Programmable Logic Controllers), SCADA (Supervisory Control And Data Acquisition), DCS (Distributed Control Systems).
- Experience with automation software/tools such as Siemens, Rockwell or Emerson.
- Familiarity with industry guidelines standards/regulations including GAMP,GMP,FDA,and EU regulations.
If this role is of interest to you, please apply now!