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Quality Engineer
Job in
Braunton, Barnstaple, Devon, EX31, England, UK
Listed on 2026-09-13
Listing for:
Jobtailor
Full Time
position Listed on 2026-09-13
Job specializations:
-
Quality Assurance - QA/QC
Quality Engineering, QA Specialist - Analyst/Manager, Quality Control - QC Analysts/Managers, Regulatory Compliance Specialist
Job Description & How to Apply Below
- Act as the Quality lead for assigned production issues and strategic quality themes
- Maintain oversight of assigned quality themes and recurring quality issues, identifying trends, emerging risks and systemic failure modes
- Connect learning across deviations, complaints, audits and operational events to ensure sustainable risk reduction and continuous improvement
- Provide Quality leadership and oversight during significant quality issues, investigations and escalations
- Challenge investigation scope, root cause analysis and proposed actions
- Support development and implementation of risk-based operational quality controls and processes
- Monitor effectiveness of improvements and elevate recurring issues or ineffective controls
- Partner with Operations and other functions to identify, understand and manage quality risks
- Provide Quality input to change controls, validation activities and operational improvement initiatives
- Support site quality governance through data analysis, trend monitoring and risk-based recommendations
- Undertake other reasonable duties as required to support the Perrigo business
- Must hold a degree or equivalent qualification in a science, engineering or related discipline
- Experience with in a regulated manufacturing environment, preferably pharmaceutical or healthcare
- Knowledge of pharmaceutical legislation
- Good understanding of GMPs, Quality Systems and Quality Risk Management Principles
- Experience analysing quality data, trends and recurring issues to identify improvement opportunities
- Strong investigation, problem-solving and root cause analysis skills
- Effective technical writing and communication skills
- Ability to influence cross-functional teams and provide constructive challenge
- Proficient in Microsoft Office applications
- All application materials, including resumes and CVs, must be submitted in English
Demonstrates expertise in Quality Leadership, Risk Management, and Continuous Improvement within regulated manufacturing environments, particularly in pharmaceuticals. Proficient in data analysis and effective communication to influence cross-functional teams and drive quality enhancements.
Highest-signal resume keywords- Quality Leadership
- Root Cause Analysis
- GMP Knowledge
- Quality Risk Management
- Data Analysis
- Quality Systems
- Quality Control Processes
- Root Cause Analysis
- Data Analysis
- Trend Monitoring
- Quality Improvement
- Regulatory Compliance
- Pharmaceutical Legislation
- Risk-Based Recommendations
- Technical Writing
- Problem-Solving
- Effective Communication
- Influencing Skills
- Regulated Manufacturing
- Pharmaceutical
- Healthcare
- GMPs
- Quality Governance
- Microsoft Office
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