Project Engineer

Apply now
Job type
Contract
Location
Sligo, County Sligo, Ireland
Ref. No
38956
Project Engineer - Ireland, Sligo - 12 Month Contract

Located on the picturesque west coast of Ireland, our Global pharmaceutical client is looking for a Project Engineer to join their state-of-the-art pharmaceutical facility. They have invested $55 billion in research to discover and develop new medicines in the pursuit of scientific breakthroughs and changing people’s lives. They have 50,000 employees around the world and are continuing to grow.

What you’ll do:
  • To provide Engineering services to the plant, in order to maximise the availability of all Site Process Equipment and Utilities.
  • To manage capital engineering projects within site following the Project Lifecycle approach (typical project value range: anything up to €5 million).
  • To support the engineering teams in controlling uptime of process equipment and optimizing efficiencies both in equipment and process performance.
  • To support the Engineering team with the emphasis on continual operational improvements.
What you’ll need:
  • Degree in a relevant Engineering Discipline (Mechanical/Chemical/Process)
  • Extensive strong site experience in API Manufacturing / OSD Manufacturing / BioPharm but will consider more junior (3 years) if they have relevant project site experience.
  • Proven track record in delivering Capital Projects – new equipment, utilities, facilities, etc.
  • Good knowledge of change control and C&Q processes/execution.
If this role is of interest, please apply now!
#LI-JS4

Apply now

Please complete the form for your job application, or feel free to reach out to our consultant directly for assistance.

Contact us

James Smithson
Business Development Consultant
James Smithson

Jobs you might be interested in

Electrical Maintenance Technician

ContractDublin, County Dublin, Ireland

Electrical Maintenance Technician - Ireland, Dublin - 12 Month ContractOne of the top 10 best companies to work in Ireland is looking for a Electrical Maintenance Technician for their large-scale new facility in Dublin. Is this you? An exciting project there is lots of opportunity to learn new technology and develop current skills within a fast paced €1 billion project. This fantastic client offers the opportunity to work within a large-scale environment with cutting edge technology.What you’ll do: Work Safely – identify risks and put in place mitigation actions if required.Ensure that equipment failures or issues are responded to promptly and appropriately in a cross functional environment.Record interventions including failure codes. Provide guidance and solutions for preventative action where required.Execute planned maintenance routines including predictive, preventative and calibration activities. What you’ll need: The successful candidate must possess at minimum a FETAC Level 6 Electrical qualification or equivalent and have a mechanical aptitude.Extensive experience in a maintenance or relevant engineering role in a regulated manufacturing environment.Experience in a regulated biopharmaceutical, pharmaceutical, medical device, facilities maintenance or FMCG facility is required.High level of attention to detail in following procedures and must be flexible and open to change. If this role is of interest, please apply now!#LI-AJ1

Senior CQV Engineer

ContractCopenhagen, Denmark

Senior CQV Engineer - Denmark, Copenhagen - 12 Months Initial Contract Our global engineering client specialise in delivering innovative solutions for the pharmaceutical and life sciences industries. Their focus is on designing and optimising advanced facilities that enable the development and production of critical medicines. With a strong commitment to quality, sustainability, and cutting-edge technology, they help clients bring life-changing treatments to patients worldwide. They are currently looking for a Senior CQV Engineer to join their team in Copenhagen.What you'll do: Coordinate Mechanical Completions Line Walks, ensuring readiness for commissioning.Oversee the development and execution of IQ/OQ/PQ protocols, ensuring compliance with GMP and regulatory standards (FDA, EMA, MHRA).Facilitate daily board meetings, providing clear updates on progress, risks, and mitigation strategies.Collaborate with cross-functional teams (Engineering, QA, Operations) to ensure seamless system integration.Manage project documentation, including qualification reports, deviation logs, and risk assessments. What you'll need: Bachelor’s degree in Engineering (Mechanical, Electrical, Chemical) or Life Sciences.Advanced degrees or certifications (e.g., PMP, Lean Six Sigma) are a plus.Extensive experience in commissioning and qualification, preferably in biopharma or regulated industries.Proven experience in leading large-scale projects, including planning, execution, and delivery.Strong understanding of commissioning of Clean & Black utilities.Familiarity with GMP, GEP, FDA, and EU regulations. If this role is of interest, apply now!#LI-DC1