At a Glance
- Tasks: Support quality and regulatory processes, ensuring ISO13485 readiness and FDA compliance.
- Company: Taylorollinson, a leading MedTech company in Manchester.
- Benefits: Hybrid work model, competitive salary, and opportunities for professional growth.
- Other info: Collaborative environment with a focus on continuous improvement.
- Why this job: Join a dynamic team and make a difference in the MedTech industry.
- Qualifications: Experience in QA/RA documentation and a passion for quality compliance.
The predicted salary is between 60000 - 70000 £ per year.
Taylorollinson is seeking a Quality & Regulatory Associate in Manchester to support the QMS and regulatory processes as ISO13485 readiness and FDA preparation progress.
The role focuses on QA/RA documentation, design controls and CAPA to ensure quality compliance across the business.
You will collaborate with cross-functional teams, maintain documentation and drive continuous improvement, with hybrid on-site expectations and a min of three days on site per week in Manchester.
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Hybrid MedTech QA/RA Specialist — ISO13485 & FDA Ready in Manchester employer: Taylorollinson
At Taylorollinson, we pride ourselves on being an excellent employer that fosters a collaborative and innovative work culture in the heart of Newcastle. Our commitment to employee growth is evident through mentorship opportunities and professional development programmes, ensuring that our team members thrive in their careers while contributing to impactful research in histopathology. With a competitive salary and a supportive environment, we offer a rewarding experience for those looking to make a difference in the scientific community.
