Quality Engineer – Cork
The successful Quality Engineer will be qualified with a Bachelor’s degree in Engineering, Quality Management, Life Sciences, or a related field.
A minimum of 2 years of experience in quality engineering or quality assurance in a regulated environment, preferably within the pharmaceutical or biotechnology sector.
Strong understanding of quality management systems (QMS), Good Manufacturing Practices (GMP), and regulatory requirements (FDA, EMA).
Proficient in quality tools and methodologies (e.g., Six Sigma, Root Cause Analysis).
Key Responsibilities:
Quality Assurance:
* Develop, implement, and maintain quality assurance processes and protocols for facility operations.
* Conduct regular audits and inspections of facility equipment and processes to ensure compliance with industry standards and internal policies.
Documentation and Reporting:
* Prepare and maintain comprehensive documentation related to quality systems, including procedures, work instructions, and reports.
* Analyze quality control data and provide regular reports to management on quality performance metrics.
Risk Management:
* Identify potential quality risks and develop strategies to mitigate them.
* Participate in risk assessments and failure mode effects analysis (FMEA) for facility projects.
Continuous Improvement:
* Drive continuous improvement initiatives within the Facilities Team to enhance quality processes and performance.
* Monitor industry trends and integrate best practices into facility operations.
Arcadis | DPS Group is an Equal Opportunities Employer.
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