Senior CQV & CSV Validation Specialist

Senior CQV & CSV Validation Specialist

Full-Time 50000 - 65000 Β£ / year (est.) No working from home possible
Bespak Limited

At a Glance

  • Tasks: Support commissioning, qualification, and validation of facilities and processes.
  • Company: Bespak Limited, a leader in Quality Operations Validation.
  • Benefits: Private medical insurance, pension contributions, and a well-being programme.
  • Other info: Opportunity for continuous improvement and career growth.
  • Why this job: Join a dynamic team and ensure compliance with cGMP regulations.
  • Qualifications: Experience in validation processes and strong collaboration skills.

The predicted salary is between 50000 - 65000 Β£ per year.

Bespak Limited in the United Kingdom is seeking a Senior Validation Specialist to join our Quality Operations Validation team. The successful candidate will support the commissioning, qualification, and validation of facilities, equipment, and processes while ensuring compliance with cGMP regulations.

This role involves collaboration with cross-functional teams, oversight of validation lifecycle documentation, and driving continuous improvements in validation processes.

Generous benefits include private medical insurance, a pension contribution, and a well-being programme.

Senior CQV & CSV Validation Specialist employer: Bespak Limited

Bespak Limited is an exceptional employer that prioritises the well-being and professional growth of its employees. With a strong focus on collaboration and continuous improvement, our Quality Operations Validation team offers a supportive work culture enriched by generous benefits such as private medical insurance and a robust pension scheme. Located in the UK, we provide a dynamic environment where you can thrive in your career while contributing to meaningful projects in compliance with cGMP regulations.

Bespak Limited

Contact Details:

Bespak Limited Recruitment Team

We think you need these skills to ace Senior CQV & CSV Validation Specialist

Commissioning
Qualification
Validation
cGMP Compliance
Cross-Functional Collaboration
Validation Lifecycle Documentation
Continuous Improvement