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    • Minimum 2-5 years’ experience working at an Engineering level, ideally in Medical Device industry or other highly regulated environment desirable.
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    • Work with cross-functional teams to identify and resolve production/engineering issues.
    • Minimum 2-5 years’ experience working at an Engineering level, ideally…
  • View similar jobs with this employer
    • Work with cross-functional teams to identify and resolve production/engineering issues.
    • Minimum 2-5 years’ experience working at an Engineering level, ideally…
    • Experience working in diagnostics, biomedical devices, biotechnology, or a related regulated industry.
    • The successful candidate will contribute to the design,…
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    • Minimum of 2 years' experience in a relevant engineering role.
    • Collaborate with-in a multidisciplinary engineering team to solve complex product development…
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    • Experience leading or supporting engineering projects.
    • Bachelor's degree in Mechanical, Biomedical, or related engineering discipline.
    • Qualified to at least degree level in Biomedical Science, Biochemistry, Immunology or a Life Science.
    • Location*: Unit D/E, 21 Time Place, Corrig Road, Sandyford…
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    • Experience leading or supporting engineering projects.
    • Bachelor's degree in Mechanical, Biomedical, or related engineering discipline.
    • Liaison with quality and engineering both internal to the plant and externally within the corporation.
    • Minimum 2-5 years’ experience working at an Engineering…
    • Currently pursuing a bachelor’s or master’s degree in biomedical engineering, Mechanical Engineering, Electrical Engineering, or a related technical discipline.
    • Extensive plant engineering leadership experience in the pharmaceutical industry, with a strong understanding of sterile drug manufacture and cGMP requirements.
    • PhD or advanced degree in molecular biology, pathology, biomedical engineering, or related translational/biomedical science field.
    • Knowledge of industrial engineering, line balancing, lean or six sigma.
    • Experience in providing technical direction, coaching and mentorship to engineering…
    • Ideal candidates for this post will have a primary degree in Aeronautical/Aerospace Engineering or a closely related area and a doctoral degree (level 10 NFQ)…
    • Responsible for supporting the development and commercialisation of next-generation minimally invasive medical devices for the treatment of coronary artery…

Job Post Details

Manufacturing Engineer - job post

Cregg Recruitment Ltd
4.4 out of 5 stars
Galway, County Galway

Location

Galway, County Galway

Full job description

Manufacturing Engineer - Galway (Hybrid)

About the role:

Our Galway based client are now hiring for a Manufacturing Engineer (Hybrid) to join their projects team. An excellent opportunity to work with a leading Medical Device company offering great career progression opportunities. The successful candidate will provide daily support of products, processes, materials, and equipment in order to achieve production goals along with develop and implement manufacturing business improvement projects and processes.

Responsibilities:
  • Analyse processes, product, material or equipment specifications and performance requirements.
  • Under broad supervision / guidance compiles and analyses operational, test and experimental data to establish performance standards for newly implemented or modified products / processes.
  • Process & Equipment validations - IQ OQ PQ
  • Project management skills
  • Troubleshoots new products / process working closely with product development.
  • Continuous Improvement & Yield Analysis, LEAN Mfg.
  • Continually seeks to drive / improvements in process design, layout and operational performance.
  • Engaging with technicians, operators, and other cross-functional teams to ensure business process success.
  • Contribution in NPI (New Product Introduction) development
  • Execute new equipment introductions and carry out validations.
  • Root cause analysis using Lean tools and techniques.
  • Writing and improving process procedures.
  • PCA (Process Change Analysis) From Documentation to Implementation
  • Demonstrates good working knowledge and application of validation techniques and associated regulatory requirements.

Qualifications and Experience:
  • NFQ Level 8 in a Technical Discipline (Science, Biomedical, Mechanical, Manufacturing, etc.)
  • Minimum 2-5 years’ experience working at an Engineering level, ideally in Medical Device industry or other highly regulated environment desirable.
  • Project Planning/Management experience highly desirable.
  • Process & Equipment validations desirable IQ/OQ/PQ

For more details please contact Gary Keane
garykeane@cregg.ie
086-1030418

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