Medical Internship jobs in London

Fairfax Medical Products Ltd is a small manufacturer dedicated to quality, reliability, and customer service. We foster a friendly, supportive workplace where we appreciate every team member. As a medical product manufacturer, we uphold high standards and provide clear instructions, practical training, and ongoing support to our staff.

Role and Main Responsibilities

• Working with Quality Management consultant
• Maintain the ISO 13485-accredited Quality Management System (QMS).
• Ensure compliance with applicable national and international standards and regulations, including ISO 13485 and 21 CFR 820.
• Maintain accurate, up-to-date, and accessible records and procedures required by ISO 13485 and CFR 820.
• Ensure company quality policies and procedures are implemented and followed by all employees.
• Promote awareness of regulatory requirements and quality practices throughout the organisation.
• Manage Corrective and Preventive Actions (CAPA), non-conformances, and complaints, from initiation through resolution, including root cause analysis and effectiveness checks.
• Prepare and present annual trend reports on CAPAs, non-conformances, and key quality indicators.
• Review, update, and maintain Standard Operating Procedures (SOPs) to ensure QA and production processes remain compliant, accurate, and well-communicated.
• Manage document and product change controls from initiation through approval and implementation.
• Support internal and external audits, including preparation, execution, reporting, and close-out activities.
• Review and maintain supplier and customer quality documentation, including verification of purchased products, approval of reports/results, and compliance checks.
• Oversee calibration and maintenance schedules to ensure timely execution.
• Support validation activities for new equipment and processes.
• Liaise with notified bodies and competent authorities as required.
• Support regulatory submissions, registrations, market approvals, and reporting to authorities.

Skills and Experience

Essential

· Basic knowledge of computers and Office 365

• Working knowledge of ISO 13485.
• Being able to work within an established Quality Management System.

Desirable

• Experience in a Quality Management System role within the medical device industry.
• Experience working in controlled environments (e.g., cleanrooms).
• Knowledge of sterilisation processes.
• Experience preparing and maintaining technical documentation (MDR).
• Working knowledge of MDR and UK MDR 2002

Pay: £15.00-£18.00 per hour

Expected hours: 16.0 – 24.0 per week

Benefits:

• Casual dress
• Free parking
• On-site parking

Experience:

• Quality Managment System ISO 13485: 1 year (required)

Work authorisation:

• United Kingdom (required)

Work Location: In person