At a Glance
- Tasks: Ensure product quality and safety through data-driven insights and problem-solving.
- Company: Global medical device organisation focused on innovation and patient care.
- Benefits: Competitive salary, career growth, and the chance to make a real impact.
- Other info: Collaborative culture with opportunities for continuous improvement and professional development.
- Why this job: Join a team dedicated to improving patient outcomes with high-quality products.
- Qualifications: Experience in regulated environments and strong knowledge of Quality Management Systems.
The predicted salary is between 40950 - 50050 £ per year.
Join a global medical device organisation where quality is at the heart of innovation and patient care. This role offers the opportunity to work across the full product lifecycle, supporting quality systems, manufacturing processes, risk management activities, and continuous improvement initiatives that help ensure safe, effective products reach patients worldwide.
Working closely with cross-functional teams, you will play a key role in driving product and process quality, investigating non-conformances, leading CAPA activities, and supporting validation and regulatory compliance efforts. You’ll have the opportunity to make a tangible impact, using data-driven insights and problem-solving skills to enhance quality performance and operational effectiveness.
This position would suit a proactive quality professional with experience in a regulated medical device environment who is passionate about delivering high standards, improving processes, and contributing to products that genuinely improve patient outcomes.
Key Skills & Experience:
- Experience working within a regulated medical device, pharmaceutical, or healthcare manufacturing environment
- Strong knowledge of Quality Management Systems (QMS) and applicable regulatory requirements
- Experience with CAPA, non-conformance investigations, and root cause analysis methodologies
- Understanding of risk management principles and ISO 14971
- Exposure to process validation activities, including IQ/OQ/PQ
- Experience supporting audits and regulatory inspections
- Ability to analyse quality data and identify improvement opportunities
- Knowledge of Lean, Six Sigma, or continuous improvement methodologies
- Strong communication skills with the ability to work effectively across cross-functional teams
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