Senior CSV Compliance Lead - GxP Validation

Senior CSV Compliance Lead - GxP Validation

Full-Time 60000 - 80000 Β£ / year (est.) No working from home possible
ConvaTec Inc

At a Glance

  • Tasks: Lead GxP compliance and validation for IT-managed systems in a dynamic environment.
  • Company: Convatec, a leading company in healthcare innovation.
  • Benefits: Competitive salary, health benefits, and opportunities for professional growth.
  • Other info: Join a team dedicated to improving patient outcomes and driving innovation.
  • Why this job: Make a significant impact on product quality and compliance in healthcare.
  • Qualifications: Experience in GxP compliance and strong leadership skills.

The predicted salary is between 60000 - 80000 Β£ per year.

Convatec in the United Kingdom is seeking a Senior Compliance Advisor to ensure IT-managed Gx P computerized systems and infrastructure are validated.

You will oversee validation activities, ensure inspection readiness, and align solutions with user and regulatory requirements.

You will develop validation strategies, QA documentation, and training to support development, manufacture, and distribution of products while maintaining compliance with major Gx P standards.

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Senior CSV Compliance Lead - GxP Validation employer: ConvaTec Inc

At Convatec, we pride ourselves on being an excellent employer, offering a dynamic work culture that fosters continuous improvement and innovation. Our Deeside and Rhymney manufacturing sites provide a collaborative environment where employees can thrive, with ample opportunities for professional growth through training and development programmes. We are committed to maintaining a diverse and inclusive workplace, ensuring that every team member feels valued and empowered to contribute to meaningful projects that make a difference in the medical device industry.

ConvaTec Inc

Contact Details:

ConvaTec Inc Recruitment Team

We think you need these skills to ace Senior CSV Compliance Lead - GxP Validation

GxP Compliance
Validation Strategies
QA Documentation
Inspection Readiness
Regulatory Requirements
Training Development
IT System Validation