• 14 Danville Business Park, Kilkenny, R95 F727, Ireland
  • +353 56 779 0100
  • info@prochem.ie
  • North Valley Business Centre, Cork, T23 KC67, Ireland     +353 21 206 6178     info@prochem.ie
  • C&Q Lead Engineer – Co. Tipperary

    Role Purpose:


    • A new vacancy has arisen for a Commissioning & Qualification Lead Engineer to join our client’s busy pharmaceutical facility in Co. Tipperary.
    • The successful candidate will manage a team of C&Q Engineers on high profile client site throughout the project lifecycle.
    • The candidate will be a convincing communicator with strong interpersonal skills to lead a team of Commissioning and Qualification engineers.


    Core Duties and Responsibilities:


    • Manage a team of C&Q Engineers on high profile client site throughout the project lifecycle.
    • Identify the appropriate Commissioning and Qualification strategy to apply on specific project and define the list of activities required.
    • Review and follow-up technical documentation from the early design phase in order to ensure alignment with GMP and CQV requirements.
    • Investigate and resolve technical issues with assistance from engineers and/or suppliers.
    • Ensure site project execution is undertaken in compliance with company guideline, department procedures and safety standards.
    • Be familiar with the Mechanical Completion procedure and Construction scope of work (Walkdown, system acceptance, punch list and follow up).
    • Schedule preparation and progress review.
    • Organize and review daily activities of other CQV Engineers assigned to the project.
    • Project management principles to coordinate CQV activities and reporting to Company and Clients PM.
    • Contractors and Vendors management and coordination.
    • Final Handover reports to the Client users


    Education & Qualifications Required:


    • Bachelor of Engineering or Science Degree in Engineering or Technology related discipline.
    • Extensive C&Q experience, including a C&Q leadership role and/or validation leadership within Pharmaceutical / Biotech industry.
    • Minimum 5 years of relevant experience with supervisory / management.
    • Delta-V experience is desirable, running EM’s and CMs.
    • API experience required
    • Strong trouble shooting experience
    • Knowledgeable with latest industry standards and guidelines on C&Q.
    • Proven knowledge and experience of working in strongly regulated GMP environment.
    • Fluent in English, written and verbal.
    • Ability to understand project plans and schedules.
    • Strong interpersonal and communication skills (verbal/written).


    To Apply: Quote – PE23067


    If you would like to discuss this vacancy or to discuss your career and other job opportunities in confidence, contact us:

    14 Danville Business Park, Kilkenny, R95 F727, Ireland.
    +353 56 77 90100

    Click here to submit your CV

    Please note, we do not require agency assistance with this role.