Project Engineer

  • Location
    Ireland
  • Type
    Permanent
  • Salary
    Competitive Package
  • Contact
    Jonaid Faheem
  • Telephone
    +44 (0) 7393 858 727
  • Email

Job Specification

Key Responsibilities For This Role Include

  • Reporting to the Engineering Director or assigned line manager. The overall objective of this role is to partake, validate and support a portfolio of project activities on site including new process installations, process modifications and process improvements relating to packaging operations unit. Which could involve involvement in preliminary & detailed design, detailed project plans, regulatory compliance, validation and installation of equipment, progress updates & KPI’s, and the overall support of projects safely, in compliance, on time, in full & within budget with local and external teams.
  • Supporting capital projects team for on-site based projects for Oral Solids Dose Manufacturing, Facilities and Packaging operations.
  • Supporting & executing Validation support activities on site across
  • Partaking or leading potential Continuous improvement programs, Process mapping and gap analysis. Optimization of existing processes to achieve desired targets.
  • Project scoping and gap analysis.
  • Delivering projects and assigned duties on time and on budget.
  • Coordinating changes using the approved change control procedure to ensure that cGMP is adhered to.
  • Support validation activities for project activities including review of validation documentation and attendance at validation activities
  • Design and write summaries for regulatory compliance or project specific
  • Update project details on a regular basis
  • Reporting into the Engineering Director and Site Projects Manager

The Minimum Qualifications For This Role Are

  • A bachelor’s degree in engineering.
  • Minimum 2-5 years’ experience in a Pharmaceutical / Food role as a Project/Packaging Engineer
  • Ability and proven track record in working and managing multiple departmental teams for operational and capital projects.
  • Background in Oral Solid dose Manufacturing & Packaging would be advantageous.
  • Must possess excellent technical writing ability
  • Strong documentation skills
  • Experience in cGMP, general packaging systems and serialization is advantageous.
  • Will require some travel within Europe, depending on project but will be minimal.
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