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
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Support day-to-day visual inspection operations in compliance with cGMP and safety standards.
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Develop, review, and optimise inspection and manufacturing procedures.
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Participate in validation and commissioning activities for processes, equipment, and facilities.
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Lead and facilitate FMEAs and oversee technician certification for inspection operations.
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Build and maintain defect libraries and perform defect trending and analysis.
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Ensure procedures align with global and regulatory requirements.
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Collaborate with internal teams and external partners to evaluate defects and support new product introductions.
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Investigate process deviations and drive corrective and preventive actions.
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Supervise external contractors where required.
Requirements
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Level 8 Degree (or higher) in Engineering, Science, or a related discipline.
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Minimum 3 years' experience in a pharmaceutical or biotech manufacturing environment.
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Knowledge of biotechnological processes, fill-finish, lyophilisation, or sterilisation preferred.
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Familiarity with semi-automated visual inspection equipment.
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Strong problem-solving and analytical skills with a continuous improvement mindset.
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Excellent communication and interpersonal abilities.
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Understanding of cGMP, ISO, and FDA regulations is highly desirable.
What's on Offer
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A collaborative, inclusive workplace focused on innovation and quality.
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Opportunities for professional growth and technical development.
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The chance to contribute to life-changing healthcare solutions in a high-performing team.
