Visual Inspection Engineer
| Job Type | Permanent |
| Location | Sligo |
| Area | Sligo, Ireland |
| Sector | Engineering |
| Start Date | |
| Advertiser | Zara Keane |
| Telephone | 094 928 8706 |
| Job Ref | 3845 |
| Job Views | 16 |
- 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.
