Visual Inspection Engineer - Pharma

    SligoPermanentCompetitive
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    Nov 5
    JN -112025-1991514

    Visual Inspection Engineer - Pharma

    Sligo Permanent Competitive

    About the job

    Visual Inspection Engineer - Sligo

    Are you an experienced Engineer or Scientist with a passion for quality and continuous improvement? This is an exciting opportunity to join a leading global biopharmaceutical manufacturer at their state-of-the-art facility in Sligo, where you'll play a key role in maintaining the highest standards of product quality and compliance.

    About the Role

    As a Visual Inspection Engineer, you will support inspection operations to ensure all manufacturing and quality processes meet safety, regulatory, and organisational standards. You'll lead process improvements, support equipment validation, and play a vital role in introducing new semi-automated visual inspection systems on site.

    This position offers the opportunity to make a tangible impact in the production of life-changing medicines, while developing your skills in a dynamic, supportive, and innovative environment.

    Key Responsibilities

    • Support day-to-day visual inspection operations in compliance with cGMP and safety standards.

    • Develop, review, and optimise inspection and manufacturing procedures.

    • Participate in validation and commissioning activities for processes, equipment, and facilities.

    • Lead and facilitate FMEAs and oversee technician certification for inspection operations.

    • Build and maintain defect libraries and perform defect trending and analysis.

    • Ensure procedures align with global and regulatory requirements.

    • Collaborate with internal teams and external partners to evaluate defects and support new product introductions.

    • Investigate process deviations and drive corrective and preventive actions.

    • Supervise external contractors where required.

    Requirements

    • Level 8 Degree (or higher) in Engineering, Science, or a related discipline.

    • Minimum 3 years' experience in a pharmaceutical or biotech manufacturing environment.

    • Knowledge of biotechnological processes, fill-finish, lyophilisation, or sterilisation preferred.

    • Familiarity with semi-automated visual inspection equipment.

    • Strong problem-solving and analytical skills with a continuous improvement mindset.

    • Excellent communication and interpersonal abilities.

    • Understanding of cGMP, ISO, and FDA regulations is highly desirable.

    What's on Offer

    • A collaborative, inclusive workplace focused on innovation and quality.

    • Opportunities for professional growth and technical development.

    • The chance to contribute to life-changing healthcare solutions in a high-performing team.