Lead quality assurance for Albus Health's medical technology platform through quality management systems, compliance, and regulated-device expertise. This part-time role offers hybrid or remote work, with Oxford onsite availability.
As Quality Assurance Manager, you will lead Albus Health's quality and compliance function within the Regulatory department. You will report to the Head of QARA while supporting product and services environments. The work covers medical devices, CSV/GAMP5, GCP, information security, and continuous improvement.
Key Responsibilities:
- Lead organisational quality and compliance functions
- Manage and own the quality management system
- Align compliance with organisational strategy and direction
- Approve deliverables under the approval matrix
- Guide CAPA/NC, training, RFx, and improvement activities
Requirements:
- Six to eight years in regulated environments
- Medical devices and CSV/CSA/GAMP5 experience
- Strong life sciences quality and compliance management experience
- Knowledge of pharmaceutical clinical-trial vendor requirements
- Experience upgrading quality systems and business controls
Apply quality leadership, medical-device knowledge, and compliance expertise to strengthen Albus Health's regulated technology operations.
Quality Assurance Manager Medical Devices in Oxford employer: Albus Health
Albus Health is an exceptional employer, offering a unique opportunity to work at the forefront of health data technology in a collaborative and innovative environment. With a strong focus on employee autonomy and growth, you will have the chance to take ownership of critical testing functions while enjoying flexible working arrangements in the vibrant city of Oxford. Our commitment to employee well-being is reflected in our generous benefits package, including share options, flexible hours, and regular team activities that foster a supportive work culture.
