Visual Inspection Engineer

https://www.teamhorizon.ie/job-search/1738-visual-inspection-engineer/engineering/sligo/job2026-02-11 11:12:102053-06-27Team Horizon
Job TypePermanent
LocationSligo
AreaSligo, IrelandSligoIrelandSligo
SectorEngineering
Start Date
AdvertiserZara Keane
Telephone094 928 8706
Job Ref3845
Job Views16
Description

Visual Inspection Engineer


Team Horizon is seeking a Visual Inspection Engineer for a client in Sligo to support visual inspection operations.


Why you should apply:



  • This is an excellent opportunity to join a world class manufacturing operation, with an outstanding track record of reliably delivering high-quality medicines to patients around the world suffering serious illnesses.

  • There is a strong culture of continuous improvement and innovation within the company to strive for solutions that improve health outcomes and dramatically improve people’s lives.

  • Our client is developing the capability to produce all its medicines, helping to ensure continuity of supply of our medicines as they expand internationally.


What you will be doing:



  • Support Visual Inspection operations to meet all safety, regulatory, and organizational standards

  • Develop and optimize procedures to enhance manufacturing processes.

  • Participate in process, equipment, and facilities validation projects; review and execute commissioning and validation protocols to keep projects on schedule.

  • Support the introduction of new Semi Automate visual inspection equipment on site and associated training

  • Lead and facilitate FMEAs for Visual Inspection, and drive the certification of technicians.

  • Build and maintain defect libraries and execute trending for defect analysis.

  • Ensure local procedures align with global guidelines and regulatory expectations

  • Provide technical leadership and guide the development of SOPs for visual inspection.

  • Collaborate with internal and external stakeholders to evaluate particles/defects and support technical transfers for new product introductions.

  • Investigate process deviations and support the production team in achieving output and yield targets.

  • Ensure full compliance with quality, safety, cGMP, and regulatory policies.

  • Supervise external contractors as required.


What you need to apply:



  • Hold a Level 8 degree (or higher) in Engineering, Science, or a relevant technical discipline. 

  • Minimum 3 years' experience in a biotech or pharmaceutical manufacturing environment—experience with biotechnological drug processes, fill finish, lyophilisation, and sterilisation preferred. 

  • Strong problem-solving and innovative thinking skills under pressure.

  • Familiarity with Semi Automated Visual inspection equipment 

  • Exceptional attention to detail and commitment to quality.

  • Excellent communication and interpersonal skills; proven ability to work both independently and in cross-functional teams.

  • Leadership qualities with a results-driven mindset. 

  • Demonstrate integrity, a strong work ethic, and the ability to work autonomously. 

  • Familiarity with cGMP, ISO, FDA regulations, and EHS best practices preferred.

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Zara Keane
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