Quality Engineer - Medical Devices Manufacturing

Baxter; Tetford; On-site; GBP 40,000 - 55,000; Full time

Benefits offered by this job

25 days annual leave + bank holidays

Blue light card

Fantastic internal progressionOpptys

Subsided canteen

Westfield healthcare

Up to 8% pension contribution

Employee assistance programme

Job summary

Baxter Thetford is seeking a Quality Engineer to join the Quality Manufacturing team to ensure life-saving healthcare products meet the highest standards of quality, compliance and safety. This role entails driving improvements and supporting regulatory readiness across manufacturing operations.

You will perform QA tests, review processes, manage change controls and collaborate with batch release and operations to resolve issues, with clear pathways for internal progression and professional

Qualifications

• Qualified in a Scientific or Engineering degree.
• Experience with quality improvement tools and data analysis.
• Experience with equipment calibration.
• Manufacturing & QA exposure; stakeholder engagement.

Responsibilities

• Perform QA tests and leak analysis and related QC activities.
• Review quality processes and procedures; advise on compliance with regulatory requirements.
• Review atypical events and complaints; initiate local holds as needed.
• Complete Quality Systems/QA commitments.
• Collaborate with Batch release teams and operations.
• Conduct continual improvement and compliance monitoring (Gembas).
• Assess change controls and approve quality modifications.
• Investigate and approve Quality NCRs; own CAPA and change control.

Skills

Quality tools

Data interpretation

Stakeholder management

Investigation ownership

QA testing

Education

Scientific or Engineering degree

Tools

Trackwise

Calibration knowledge

Job description

Baxter Thetford is seeking a Quality Engineer to join the Quality Manufacturing team to ensure life-saving healthcare products meet the highest standards of quality, compliance and safety. This role entails driving improvements and supporting regulatory readiness across manufacturing operations.

You will perform QA tests, review processes, manage change controls and collaborate with batch release and operations to resolve issues, with clear pathways for internal progression and professional