C&Q Engineer Role Carlow

Process Engineer

  • Posted Oct 18, 2021
  • Carlow
  • Contract
  • BBBH24562

Process Engineer is required for a global Biopharmaceutical company in Carlow. This is a state of the art vaccines and biologics manufacturing facility currently producing many products in various therapeutic areas including: oncology, autoimmunity, pneumonia and infectious disease. The site is less than ten years old and has been fitted with the most up to date manufacturing technology and best practices and is truly a "state-of-the-art" facility. Site activities include the development of next generation oncology products, Formulation of Vaccines & Biologics, Fill finish / Vial filling, Packaging and Global distribution.

The team on site are focused on creating an environment where excellence, innovation, quality, compliance and teamwork support their strategy to meet the needs of their global patients.
If you want to work on the leading edge of the Biotech industry then this is the opportunity for you.

The Process Engineer will be responsible for:

  • Support GES Process Lead and GES Suite Team Lead to implement a Process Design based on the scope of Process Requirements provided by the Technology and Manufacturing owners.
  • Lead package ownership for the agreed packages and facilitate cross-functional interactions to ensure project and site stakeholder inputs are reflected in vendor design deliverables.
    • Ensure all project stakeholders are informed and consulted on key process suite activities and decisions.
    • Monitor progress of package milestones with all team members and provide status reports to project Suite and Tiers.
  • Act as client owner representative to self-execute critical deliverables and oversee other deliverable by an Architect & Engineering design firm.
    • Own package technical deliverables including User Requirement Specifications, Equipment Specifications, PHA (HAZOP) Action.
    • Ensure MSD Global and Local engineering standards, procedures and practices are followed for packages.

The Process Engineer requires:

  • Minimum qualification B.Sc. or M.Sc./ M.Eng Degree in Chemical, Mechanical or Biochemical Engineering or equivalent discipline; equivalent is defined as a Biotechnology or Industrial Chemistry Degree with the basic elements of chemical/mechanical/ biochemical engineering fundamentals as applied to sterile or aseptic manufacturing.
  • Minimum of 6 years post academic process engineering experience.
  • Awareness of sterile drug product unit operation and sterile support/formulation systems is preferred.

Note: Are you currently eligible to work in Ireland? As this is a contract opportunity you will need to hold a Stamp 1G/Stamp 4 visa to apply!

Call Kieran O'Sullivan in LSC on 021 4777 329 to discuss this new Process Engineer role in more detail or apply directly via this advert.

This could be the perfect project for you! Apply online and we’ll be in contact shortly


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The benefits of contracting with LSC

  • Partners to the world’s top Life Science companies we offer you the best contract opportunities in the industry
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  • LSC’s Consultant Success Programme focuses on skills development & on-site support to help you achieve your career goals!

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