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Visual Inspection Specialist

2 weeks ago

Sligo, Sligo, Ireland beBeeTechnical Full time €50,000 - €80,000

Job Title: Visual Inspection Engineer

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This is a 12-month contract position as a Visual Inspection Engineer for a multinational biopharmaceutical client based in Sligo.

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Responsibilities:

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  • Support Visual Inspection operations, ensuring safety, regulatory compliance, and organizational standards.">
  • Develop and modify procedures to support manufacturing processes.">
  • Participate in process, equipment, and facility validation projects.">
  • Review and approve process-related commissioning, qualification, and validation protocols.">
  • Execute protocols to meet project schedules.">
  • Lead Process FMEAs for Visual Inspection as required.">
  • Establish and optimize technician certification processes for visual inspection.">
  • Maintain the defect library and execute defect trending processes.">
  • Ensure site procedures align with global and regulatory standards.">
  • Contribute to SOP development for Visual Inspection.">
  • Lead manufacturing and validation activities during projects.">
  • Coordinate with stakeholders on particle/defect evaluation.">
  • Support technical transfers for new product introductions.">
  • Investigate process exceptions and malfunctions.">
  • Collaborate with engineering and quality personnel.">
  • Support production to meet output and yield targets.">
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Required Skills and Qualifications:

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  • Degree or Masters in engineering, science, or a technical discipline.">
  • Minimum three years in technical, operations, or quality roles within pharma or healthcare manufacturing.">
  • Experience in biotech or pharmaceutical manufacturing environments.">
  • Experience with biotechnological, parenteral, or related manufacturing processes is preferred.">
  • Knowledge of clean utilities is desirable.">
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Benefits:

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  • Commitment to organizational vision and operational excellence.">
  • Supportive of a positive development culture and compliance.">
  • Self-motivated with high autonomy.">
  • Adherence to all policies ensuring cGMP and regulatory compliance.">
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Others:

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  • Operate independently with technical discretion.">
  • Present technical data for decision-making.">
  • Follow EHS policies and promote safety culture.">
  • Report incidents and participate in EHS initiatives.">
  • Attend EHS training and wear PPE as required.">
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