Head of Product Development

TN United Kingdom; United Kingdom; Remote; GBP 60,000 - 100,000; Full time

Job summary

An innovative clinical stage R&D company is seeking a Head of Product Development to spearhead the design and development of groundbreaking treatments for Solid Tumour oncology. This pivotal role not only involves leading product design but also ensuring compliance with regulatory standards and managing the creation of essential documentation. As part of the leadership team, you will collaborate closely with the CEO, driving the vision of the company forward. If you are a seasoned R&D professional with a passion for medical device innovation and are ready for a challenge that includes frequent travel to Italy, this opportunity is for you.

Qualifications

• Experience in design and development of class II and III medical devices.
• Extensive experience in product verification and validation documentation.

Responsibilities

• Lead the product design and development process.
• Ensure regulatory approval and manage QMS documentation.

Skills

Product Design

Regulatory Approval

ISO 13485 Knowledge

Team Management

Problem-Solving

Education

Degree in Medical Discipline

Degree in Scientific Discipline

Degree in Engineering Discipline

Job description

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Our client is a clinical stage R&D company that is developing an innovative treatment for Solid Tumour oncology.

We are looking for an experienced R&D professional to join the team as Head of Product development to lead the product design and development process. The main focus of the position will be ensuring the approval by regulatory authorities and QMS documentation to build the Design History File of the product.

The position is part of the leadership team and works closely with the CEO of the company.

PLEASE NOTE the company is based in Italy and frequent travel will be required.

Requirements:

• A degree in a medical, scientific or engineering discipline
• Solid experience in the design and development of class II and/or ideally class III implantable medical devices.
• Extensive experience in creating product verification and validation documentation
• Detailed understanding of ISO 13485
• Management of external partners and cross-functional teams
• High level of technical and personal capabilities; a problem-solver
• Ability to travel regularly to Italy or relocate