Our client, a leading Pharmaceutical Company in Cambridgeshire, is seeking a Quality Engineer to join their team on an initial 12 month contract. As the Quality Engineer, you will be responsible for providing subject matter expertise to medical device and combination product development programmes throughout the product lifecycle. This role offers hybrid working (50% onsite). KEY DUTIES AND RESPONSIBILITIES: Your duties as the Quality Engineer will be varied however the key duties and responsibilities are as follows: 1. As the Quality Engineer, you will lead design control and risk management activities for combination product development programmes, ensuring deliverables are appropriately authored, approved, and maintained to support clinical trials and commercial licensures. 2. As the Quality Engineer, you will support and facilitate effective risk management activities at external design companies and manufacturing facilities related to assigned projects. 3. As the Quality Engineer, you will ensure combination product development activities are compliant with quality and regulatory standards, both internal and external. 4. As the Quality Engineer, you will provide input and support to design validation including, but not limited to, human factors engineering assessments. ROLE REQUIREMENTS: To be successful in your application to this exciting role as the Quality Engineer we are loo...