About The Role
Working within our multidisciplinary teams on major product development projects, you will be responsible for supporting compliance at CDP within the ISO 13485, ISO 9001 and ISO 27001 Management System. The role also includes supporting a selection of clients on a range of products and processes in primarily the medical sector. 

You will come from a Design and Development background and have a good understanding of New Product Development/Transfer to Manufacture. A fantastic time to join the team, you will have numerous projects to get stuck into and immediately add value. This role will suit an ambitious individual who is looking for career advancement and training and development opportunities. Positive, professional and confident you will have the ability to attend client meetings and lead projects in the future.

Your duties will include:
  • Perform Internal Audits 
  • Hosting and SME at External Audits 
  • RCA facilitator for NC 
  • Owner NC/CAPA 
  • Monthly Metric Reporting 
  • Supplier Approval 
  • Support eQMS training for new starters
  • Process owner within the Management System
  • Support Production Manager to ensure compliance in the US labs 
  • Monthly Audits of the US labs 
  • Management of US assets in the eQMS
  • Presenting US QMS Induction
  • Ensure US training events are recorded and stored appropriately
  • Define project specific training plans
  • Quality   Specialist for Client Projects including New Product Development, Transfer to Manufacture and Quality Projects e.g. DHF Remediation
About You
  • Experience of working within ISO 13485 quality management system, laboratory or manufacturing background desirable. 
  • Excellent organisational skills, used to multi-tasking and able to prioritise and juggle new tasks as they arise
  • Degree qualified 
  • Ability to write technical documents in a methodical and timely manner  
  • Experience of performing reviews and approvals of documents for Quality
  • Experienced at developing content for Design History and technical files
  • Desire to lead projects and programmes, taking responsibility for quality, time and profit 
About Us
We are an employee owned company with our staff at the centre of our strategy. Employee ownership allows us to maintain full control over the direction of our business and our creative culture.

Work Authorization
Cambridge Design Partnership will only employ those who are legally authorized to work in the United States. This is not a position for which sponsorship will be provided.

Equal Opportunity Employer 
Cambridge Design Partnership is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to sex, race, color, religion, national origin, age, marital status, political affiliation, sexual orientation, gender identity, genetic information, disability or protected veteran status. We are committed to providing a workplace free of any discrimination or harassment.