This is a fantastic opportunity for a Quality and Regulatory Manager to join a Global Medical Device company based in Lancashire. Leading a team within QA/RA this will suit someone with a strong background in Medical Devices, people leadership, Regulatory Affairs and Quality Management.
Key Responsibilities & Activities
Responsibility for development, implementation and continued improvement of the quality management system and regulatory documentation.
Ensure a robust supply chain is in place to support product conformity.
Development and maintenance of Technical Documentation for regulatory purposes.
Managing the internal, supplier and 3rd party audit programmes.
Liaison with external bodies, customers and suppliers.
The UK Quality & Regulatory Manager is the appointed Management Representative.
Responsible for working within Health, Safety and Environmental standards and procedures.
Aptitude for team work and results orientation.
Aptitude and ability to promote continuous improvement in a busy manufacturing environment.
Experienced in statistical analysis techniques and application.Job Qualifications, Skills & Attitudes
Ability to plan and organise work load according to priority, business needs and strict deadlines.
Very good verbal and written communication skills.
Attention to details and excellent visual awareness.
Ability to communicate effectively with different stakeholder groups on site.
Ability to present data and information to senior manage...