Quality Inspector

Fohntech Group; Dublin; On-site; EUR 42,000 - 64,000; Full time

Job summary

Fohntech Group seeks an experienced Quality Inspector for a Belgium project. The role covers QA inspections, audits, and documentation control across ISO 9000/2000 and ISO 14001 standards. A rotation plan is available and the project duration is two years.

Ideal candidates will have a mechanical bias qualification and 3+ years on-site QA experience, with proficiency in MS Office and strong reporting skills. Pharma sector exposure is a plus.

Qualifications

• Third level or professional qualification with a mechanical bias.
• 3+ years experience with the quality walk-down process on site.
• 3+ years experience in QA inspections on large scale construction sites.
• Experience in completing inspections and forms per approved site ITPs.
• Ability to work well under pressure and meet deadlines.
• Good organisational and planning skills.
• Excellent work and personal ethics including trustworthiness and empathy.
• Confident, creative and energetic approach to addressing quality issues.
• Proficient in MS Excel, Word and PowerPoint.
• Pharma industry experience would be an advantage.

Responsibilities

• Manage, implement and maintain ISO 9000/2000 and ISO 14001.
• Develop quality plans, manuals, documents and systems.
• Ensure client QA standards and procedures are submitted, approved and implemented on time.
• Complete audits and advise management on QA issues.
• Coordinate weekly meetings with client, subcontractors and suppliers.
• Maintain documentation and certification prior to handover.
• Ensure documentation and QA/QC procedures are standardised and integrated into the QA/QC Manual.

Skills

Quality walk-downs

Organisational skills

Written reporting

Trustworthiness & ethics

Education

Mechanical bias qualification

Tools

MS Excel

MS Word

MS PowerPoint

Job description

Dublin 15, Ireland

Fohntech Group is seeking an experienced Quality Inspector to join their team in Belgium.

Rotation plan is available. Duration of the project is 2 years.

Key Responsibilities of the Role:

• Management, implementation and maintenance of ISO9000/2000 & to ISO 14001
• Develop quality plans, manuals, documents and systems
• Work with our Client to ensure that their Quality standards & procedures are successfully submitted, approved & implemented against agreed timelines
• Completion of Audits
• Advise Management on QA issues
• Ensure that all documentation and certification is complete and checked prior to final handover
• Attend and co-ordinate weekly meetings with the client, subcontractors & suppliers
• Documents Control - Reviewing and revising documentation to incorporate changes to company policies and objectives, in order to stay in line with ISO 9000/2000.
• Reporting to Project Manager
• Arranging and attending site installation inspections
• Continuous quality inspections of the works as they progress
• Arranging and attending benchmarking inspections
• Keeping “Right First Time” records / procedures up to date
• Handover of systems / areas to client’s team
• Ensuring that the current QA/QC procedures used on projects are standardised and integrated into the Company QA/QC Manual.
• All other duties associated with this role

Essential Criteria for the Role:

• A relevant Third Level or Professional Qualification with a Mechanical bias
• 3+ years experience with the Quality walk down process on site
• 3+ years experience in Quality/ QA Inspections on large scale construction sites
• Working knowledge of doing inspections and forms per approved site Inspections and test Plans
• Ability to work well under pressure and within strict deadlines
• Good organisational and planning skills
• Excellent work and personal ethics that include trustworthiness, commitment, and empathy
• Confident, creative, and energetic approach to addressing all quality-related issues
• Ability to produce quality written reports
• Proficient in the use of MS Excel, MS Word, and MS PowerPoint
• Experience in the Pharma industry would be a distinct advantage