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Manufacturing Engineering - Visual Inspection - Job Opportunity at Dillon Engineering Services

Sligo, Ireland
Contract
Mid-level
Posted: May 12, 2025
On-site
EUR 50-55 per hour

Benefits

Premium on-site parking facilities with dedicated spaces for manufacturing staff
12-month contract duration offering stability and project completion exposure
Flexible 8-hour shift schedule within standard business hours

Key Responsibilities

Lead and optimize the visual inspection certification process for manufacturing technicians, ensuring regulatory compliance and quality standards
Develop and maintain comprehensive defect library while establishing trending analysis protocols for inspection defects
Drive alignment between site-specific visual inspection procedures and global guidance documents
Manage technical transfers for new product introductions and lead validation activities throughout project lifecycle
Coordinate with internal/external stakeholders for particle/defect evaluation and process optimization

Requirements

Education

Degree Level or Masters in engineering, science or technical discipline

Experience

Minimum 3 years in Technical/Operations/Quality in Pharmaceutical/Healthcare

Required Skills

Manual Visual Inspection (MVI) expertise USP 1790 knowledge GMP Manufacturing environment experience Process validation expertise Technical documentation skills Biotechnology manufacturing process knowledge Clean utilities experience
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Sauge AI Market Intelligence

Industry Trends

The biopharmaceutical sector is experiencing increased demand for visual inspection expertise due to rising regulatory scrutiny and quality standards in parenteral drug manufacturing Automation and digital transformation in visual inspection processes are creating hybrid roles requiring both traditional inspection expertise and digital system knowledge Growing focus on particle characterization and advanced analytics is elevating the technical requirements for visual inspection roles

Salary Evaluation

EUR 85,000-95,000 annual equivalent, competitive for Irish biopharma market considering role specialization and location

Role Significance

Typically part of a 5-8 person technical operations team, interfacing with 15-20 production staff
Mid to senior technical position with significant influence on quality assurance and regulatory compliance

Key Projects

Implementation of new visual inspection protocols aligned with updated regulatory requirements Technical transfer projects for new product introductions Validation of inspection processes and equipment Development and optimization of operator certification programs

Success Factors

Deep understanding of regulatory requirements and GMP principles Strong technical documentation and process validation expertise Effective stakeholder management across quality, operations, and external partners Ability to bridge technical requirements with practical implementation

Market Demand

High demand role due to expanding parenteral drug manufacturing sector in Ireland and strict regulatory requirements for visual inspection expertise

Important Skills

Critical Skills

Visual inspection expertise with specific focus on parenteral products GMP and regulatory compliance knowledge Technical documentation and validation experience Process development and optimization capabilities

Beneficial Skills

Project management skills Statistical analysis capabilities Automation system knowledge Change management experience

Unique Aspects

Specialized focus on visual inspection in parenteral drug manufacturing
Combination of technical expertise and process development responsibilities
Direct involvement in quality system development and implementation

Career Growth

2-3 years in role typical before advancement, depending on project success and organizational growth

Potential Next Roles

Senior Manufacturing Engineer Quality Assurance Manager Technical Operations Lead Validation Manager

Company Overview

Dillon Engineering Services

Contract role through Dillon Engineering Services for a leading global biopharmaceutical company with significant Irish operations

Strong position in the Irish biopharma sector with established presence in global markets
Strategic location in Sligo supporting Ireland's growing biopharma manufacturing hub
Professional environment with focus on technical excellence and regulatory compliance
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