The company you would be working for have seen rapid growth in the last 24 months and has vast product portfolio, which includes surgical and wound care products.
As a Validation Coordinator you would be responsible for ensuring validation support to the UK based businesses and would be key to the success of the Regulatory and Quality strategy. As the ideal candidate you would have experience working in a quality or compliance role, within the medical device industry or another highly regulated industry. You would have great communication skills and knowledge of working to ISO standards and FDA CFR in a continuous improvement environment.
Main task included:
- Working with the Quality and Regulatory department to plan, schedule and conduct all identified validation projects.
- Plan validation activities in collaboration with key stakeholders
- Responsible for ensuring the UK businesses quality management system reflects practice and is kept up to date
- Work with cross functional teams providing input when required.
your application has been submitted