£24,000 - £30,000 + Company Benefits
Are you a Quality Engineer looking for training and development across multiple departments in a small, niche specialist business?
On offer is a permanent role where you will be responsible for implementing and driving quality standards, technical documentation management and ensuring that medical device compliance is adhered to.
This is a varied role where you will be working as part of a small production team, providing technical support and training, ensuring completion of activities within agreed time-lines and participate in internal or external audits.
This role would suit a Quality Engineer from a Science/Engineering background looking for training and development across multiple departments in a small, niche specialist business and a great opportunity for someone looking to advance their career.
You will be responsible for managing technical documentation, CAPA and writing/maintaining processes and procedures in compliance with ISO13485 QMS system. Verification and validation of ISO process and procedures as well as Reviewing product promotional materials, labeling, batch records, specification sheets, or test methods for compliance with applicable regulations and policies.
" A confident communicator, who has experience completing with presentations, and technical/procedural writing skills.
" Able to make effective decisions while working under pressure and to timelines.
" A positive can-do attitude and the ability to work with others on projects.
" Bachelor's degree in a Science/Engineering Discipline or equivalent
" Minimum of 1-3 years' experience in a medical device or a related field.
" Understanding of ISO13485, ISO14971, and new IVDR and MDR regulations
" Should have a solid understanding of GxP (GLP, GCP, GMP etc)
If you wish to apply or discuss further, then please contact Victoria MacDonald on 01463729213 or email