Regulatory Quality Lead: Data Integrity & ISO 13485 in Horsham

Regulatory Quality Lead: Data Integrity & ISO 13485 in Horsham

Horsham Full-Time 51750 - 63250 Β£ / year (est.) Home office (partial)
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At a Glance

  • Tasks: Lead regulatory programmes and ensure compliance with data integrity standards.
  • Company: Join Thermo Fisher Scientific, a leader in scientific innovation.
  • Benefits: Enjoy hybrid working, competitive salary, and career development opportunities.
  • Other info: Dynamic role with opportunities for growth in the life sciences sector.
  • Why this job: Make a real difference in a highly regulated environment while collaborating with diverse teams.
  • Qualifications: Experience in regulatory compliance and knowledge of ISO 13485 required.

The predicted salary is between 51750 - 63250 Β£ per year.

Thermo Fisher Scientific Horsham site is seeking a Quality Compliance Specialist to lead regulatory programmes across EU GMP (EudraLex Volume 4), FDA 21 CFR Parts 210 & 211 (cGMP), ISO 13485, and other applicable regulatory requirements. The role focuses on Data Integrity and controlled drug compliance within a highly regulated environment.

Based at the Horsham site with hybrid working, the successful candidate will collaborate with Quality, Manufacturing, Engineering and Supply Chain to embed.

Regulatory Quality Lead: Data Integrity & ISO 13485 in Horsham employer: ThermoFisher Scientific

As a Manufacturing Operator I, you will join a dynamic team committed to upholding the highest standards of safety and quality in a cleanroom environment. Our company fosters a culture of continuous improvement and teamwork, providing comprehensive training and opportunities for personal growth. With a flexible shift pattern and a focus on employee well-being, we ensure that our staff are supported and valued in their roles.

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Contact Details:

ThermoFisher Scientific Recruitment Team

We think you need these skills to ace Regulatory Quality Lead: Data Integrity & ISO 13485 in Horsham

Regulatory Compliance
Data Integrity
ISO 13485
EU GMP
FDA 21 CFR Parts 210 & 211
Quality Assurance
Collaboration Skills