
Chief Quality Specialist
3 days ago
We are seeking an exceptional Quality Engineer to join our team in ensuring customer satisfaction by monitoring, controlling and improving all related customer processes.
The primary objective of this role is to identify, plan, and organize regulatory affairs for ensuring compliance with industry standards and regulations. This includes the management of closed loop customer complaints and improvement processes.
Key responsibilities include:
- Management of DMR/DHR and Technical Files
- Data collection, analysis and reporting
- Pareto and trend analysis
- Initiate and drive Continuous Improvement programs
- NPI Approval including First Article Inspections and Reporting
To be successful in this role, you will require a minimum NFQ Level 7 Degree/Diploma in Science or Engineering, or a lesser qualification with sufficient job-related experience. At least 2-3 years Quality Assurance/Regulatory affairs experience in a similar Quality Engineering role in the electronics manufacturing industry is also required.
A sound understanding of problem-solving techniques, proficiency in Microsoft Office, good communication and influencing skills are essential. You will also have the ability to write standard operating procedures, training documents, and regulatory responses.
If you have experience in working within a Medical Device Manufacturing Environment or similar, Six sigma Green or Black Belt Certified, and experience in New Product Introduction Processes, these would be highly desirable.
This is a challenging and rewarding opportunity for a motivated and experienced Quality Engineer to make a real impact in our organization.
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Quality Assurance Specialist
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Quality Assurance Specialist
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Quality Assurance Specialist
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Quality Assurance Specialist
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Advancing Pharmaceutical Quality
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Castlebar Municipal District, Ireland beBeePharmaceutical Full time €40,000 - €60,000**Job Title:** Quality Assurance SpecialistWe are seeking a skilled Quality Systems professional to join our team. This is a key role ensuring compliance with Good Manufacturing Practice (GMP) standards and supporting quality functions across the site.Act as Subject Matter Expert for validation, change control, laboratory systems, incidents, microbiology,...