Quality Assurance Administrator

Quality Assurance Administrator (Engineering) at Endomag

Join Endomag: Shape the Future of Breast Cancer Care

Location: Cambridge Science Park, Cambridge, CB4 0WN

Hybrid: 2-3 days per week home based flexibility

Reporting to: QA Director

This QA Admin role with Endomag is being represented by Indo Search on an exclusive basis.

Why Endomag?

?? Pioneering Technology: Work with cutting-edge medical devices, including complex Class II/III and sterile technologies.

?? Meaningful Impact: Directly contribute to improving cancer care and patient outcomes.

?? Career Advancement: Thrive in a growing team with ample opportunities for professional development.

?? Continuous Learning: Benefit from a structured training programme designed to accelerate your growth.

?? Collaborative Culture: Be part of a supportive, innovative, and dynamic work environment.

Salary:

• Up to £36,000 per annum

Benefits:

• 9% non-contributory pension
• Up to 10% bonus
• Private medical insurance for you and your family
• Private dental insurance
• 25 days holiday plus an annual buy scheme for an extra 5 days
• 2 volunteering days for charity work
• Structured training for career development

About Endomag

Endomag is at the forefront of surgical guidance technology for breast cancer. Their innovative solutions, including the Sentimag® probe and Magseed® marker, are transforming patient care in over 600 hospitals across 40+ countries. Recently acquired by Hologic, Endomag is poised for even greater impact and growth.

Your Mission

As Endomag's Quality Assurance Administrator, you'll play a crucial role in bringing new products to life and enhancing their existing portfolio. You'll work closely with the Product Engineering and R&D teams to ensure seamless design reviews and product releases. Your expertise will be vital in maintaining compliance across their range of Class IIa, IIb, and Class III sterile devices.

Key Responsibilities

• Drive quality excellence in product development and improvement
• Manage design control and documentation reviews, ensuring ISO 13485:2016 compliance
• Oversee quality documentation for new products, including material and sterilisation controls
• Maintain and evolve the QMS and technical files as industry standards progress
• Support release processes for subcontracted production devices
• Collaborate across departments to uphold quality standards and regulatory compliance

Ideal Candidate

Qualifications & Experience:

• Experience with ISO quality systems in the medical device sector
• Knowledge of design control, material, and sterilisation compatibility processes
• Degree in physics, chemistry, engineering, or related field (preferred)
• Proficiency with eQMS systems
• Experience in managing design and change control under ISO 13485:2016

Skills & Attributes:

• Self-motivated with excellent organizational and time management skills
• Strong written and verbal communication abilities
• Detail-oriented with a keen eye for accuracy
• Adaptable team player comfortable in a fast-paced environment
• Proficient in MS Office suite

Bonus:

• Validation experience
• Willingness to travel occasionally within the UK and internationally

Join Endomag in their mission to revolutionise breast cancer care. Apply now and be part of a team that's making a real difference in patients' lives!

How to Apply

Apply today or contact josh@indoprofessionals.co.uk for more information.