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Medical Device jobs in Spiddal, County Galway

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    • Following procedures and carrying out reviews on documentation to meet good documentation practices for a medical device company.
    • At least 3 years previous related experience in the medical device industry.
    • Good working knowledge of medical device materials and processes, in particular…
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    • This contract position for 12-18 months has come on-stream as the company embarks on a site-wide finance programme which will see current Senior Financial…
    • The Quality Assurance Documentation Controller will be responsible for the day to day management of the site GMP documentation system, acting as administrator…
    • Degree in Biological Science or similar.
    • Advanced IT skills e.g. Microsoft Office (Word, Excel and Outlook).
    • Numerate with strong analytical and problem-solving…
    • Supports the timely approval of medical devices and maintenance of regulatory approvals for marketed products.
    • Strong written and verbal communication skills.
    • We currently have a Production Packer position on Day shift.
    • 12-month Fixed Term Contract with a strong potential of a permanent contract.
    • A third level STEM qualification preferably in chemistry, life sciences or engineering with at least one year experience in the medical device industry or…
    • Familiarity with medical device development processes and regulated environments is desirable.
    • The role of Associate Human Factors Engineer is to support the…
    • From secure device connectivity and real-time data platforms to intelligent clinical tools and patient-facing experiences, PCS transforms complex cardiac data…
    • Minimum of 4 years’ medical device manufacturing experience (at least 2 year cleanroom based) or equivalent.
    • The Manufacturing Operator will work as part of the…
    • A minimum of 2 years’ experience in all stages of medical device design and development (including design with SolidWorks, prototyping, testing).
    • Engaging Assembly Role : Rotate through assembly lines performing a variety of tasks, creating life changing medical products with precision.
    • Depending on your area of study and placement, you may support engineering, manufacturing, scientific, quality, supply chain, business, or technology…
    • Significant experience within a GMP pharmaceutical, sterile manufacturing, biologics, or medical device microbiology laboratory.
    • Have working knowledge of MODA.

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Job Post Details

Quality Control Technician - DHR Review - job post

Caragh Precision
3.5 out of 5 stars
Galway, County Galway
Permanent
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Job details

Job type

  • Permanent

Location

Galway, County Galway

Full job description

We are currently searching for someone to join our Quality Department in our company based in Parkmore Business Park, Co. Galway. This is an Entry-Level role that encompasses both Documentation Review/ Product Release. The hours 07:30-16:30 Monday to Thursday, 07:30-12:30 on Fridays.

Requirements:

  • Accuracy and good attention to detail are essential.
  • Good level of written and spoken English.
  • Mechanical aptitude an advantage.
  • Ability to work well individually and as part of a team.
  • Previous clerical/product building experience is an advantage but not essential.

General Function

Reporting to the quality cell/team lead the clerical/product builder is responsible for supporting production processes with general operational tasks.

Main Duties

  • Following procedures and carrying out reviews on documentation to meet good documentation practices for a medical device company
  • Maintaining high attention to detail at all times.
  • Achieving daily/weekly targets.
  • Adhering to Company policies and ensuring health and safety regulations are maintained at all times.

Benefits

  • Working with a small friendly team within a growing organisation.
  • Full exposure to Medical Device Industry.
  • Training

Job Types: Permanent, Full-time

Job Type: Permanent

Work Location: In person

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