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Process Engineer

Eingestellt von Modis

Gesuchte Skills: Engineer, Sales, Engineering, Autocad


Role: Lead Process Engineer

Location: Liverpool

Duration: 3 months Rolling

Rate: Negotiable


Following my clients restructure, an exciting opportunity has developed for a Lead Process Engineer within a diverse team. The role would involve the generation and control of the equipment Process and Instrumentation diagrams (P&ID), mechanical and process technical specifications for equipment design, manufacture and testing. This is a great opportunity for a diligent and technically competent individual to join a strong team at a leading Pharmaceutical manufacturer.

Skills and Experience:

Qualified to Degree level in Mechanical or Chemical Engineering. Exceptions may be made in certain circumstances where a candidate excels in other critical areas. 5 years experience in similar industrial sector.
Proficient in the generation and understanding of P&IDs using 2D Autocad/Draftsight software. Confident with all MS Office software including Excel, Word, Outlook etc.
A strong understanding of thermodynamics, fluid dynamics and all common industrial equipment including, pumps, valves, filters utilised in the Pharmaceutical industry.
Knowledge and understanding of the Pharmaceutical industry including and not limited to API processing, powder handling, Cleanroom technology, Occupational Exposure Limits (OEL), Containment Performance Testing (CPT) and FDA compliance.
Diligent individual with strong organisational and communication skills and ability to be adaptable and make decisive contributions with in a professional environment.
Great opportunity for global travel to support sales activities and gather the necessary process information for equipment design. Valid driving licence required.

Key Responsibilities (Lead Process Engineer):

Direct responsibility for the generation of Process and Instrumentation Diagrams, Equipment test protocols and process equipment technical purchasing specifications.
Contribute to the development of contract H&S assessments, Operating procedures and IQ/OQ documentation.
Controlling all regulatory documentation for equipment process compliance inclusive of Operator Exposure, Air classification, FDA regulations, CIP & SIP regimes etc.
Review of Client URS in order to develop a cost effective and efficient process system.
Technical review of contract specification and equipment General arrangement drawings to ensure compliance with P&ID and client process requirements.
Development of standard documentation to increase the efficiency of sales and preproduction activities.

If you feel this role is of any relevance to you please feel free to contact me.


  • Vertragsart:


  • Berufserfahrung:

    Keine Angabe

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