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Process Engineer

Eingestellt von Quanta Consultancy Services

Gesuchte Skills: Design, Engineering, Engineer

Projektbeschreibung

Process Engineer required to join a global biotech company for an initial 12 month contract. The Biologics Process Engineer is a key technical resource, who will support the delivery of a new biologics manufacturing facility in Dublin. Reporting to the Process Engineer manager, the Process Engineers/Process System Owners will be responsible for delivery of robust drug substance process manufacturing systems by guiding detail design, equipment selection, supporting startup & qualification activities, and the resolution of technical issues.

Role and Responsibilities:

* The Process Engineers will have ownership over a specific set of equipment systems as the project progresses through design, construction, and start-up.
* Responsible for process design to ensure delivery of assets and capacity as defined by project goals, to meet business objectives.
* Oversee detail design for system, including close management of design and fabrication of vendor systems.
* Ensure all design & project work is completed in compliance with all Regulatory requirements including Quality (cGMP, Quality Directives), EHS, Global Engineering, design & construction directives, requirements and procedures.
* Responsible for process system cost, to ensure it remains within the budget & cash flow projection forecast.
* Contribute to definition of commissioning and qualification approach.
* Responsible for regular communication across functional lines (eg Construction Manager, Automation, Quality, Utilities, etc.) to ensure design and startup activity coordination as well as resolution of technical issues.
* Assist in the management of outside contractors, assures construction & contractor safety and environmental compliance with all company policies & government regulations.

Requirements:

* The successful candidate must possess a Bachelor of Science in engineering, biologics or chemistry or related discipline.
* A minimum of 8 years of experience in the design and construction of biopharmaceutical manufacturing facilities and minimum 6 years' experience in the support of the process system operations.
* Experience in engineering support of cGMP biopharmaceutical manufacturing processes and facilities preferred.

If this is you please apply today.

Projektdetails

  • Einsatzort:

    Irland

  • Projektbeginn:

    asap

  • Projektdauer:

    12 months+

  • Vertragsart:

    Contract

  • Berufserfahrung:

    Keine Angabe

Geforderte Qualifikationen

Quanta Consultancy Services

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