Quality Manager

Iterative Health; Cambridge; On-site; GBP 45,000 - 70,000; Full time

Job summary

Iterative Health is seeking a Quality Manager to oversee quality processes in the medical device sector. The role involves ensuring compliance with FDA and ISO standards, managing quality initiatives, and collaborating with cross-functional teams to solve scientific challenges. Candidates should have a strong background in quality management and regulatory compliance.

Benefits

Vision/Dental/Medical Insurance

Life/Disability Insurance

Stock Options

Flexible Work Hours

Unlimited Paid Time Off

Qualifications

• Minimum 5 years of experience in a Quality role within a medical device.
• Strong knowledge of ISO 13485, ISO 9001, and QSR.
• Experience supporting regulatory audits and inspections.

Responsibilities

• Ensure compliance with FDA and ISO standards.
• Oversee the electronic quality management system (eQMS).
• Lead continuous improvement initiatives to enhance product quality.

Skills

Attention to detail

Problem-solving

Interpersonal skills

Regulatory compliance

Education

Bachelor’s degree

Tools

Electronic quality management systems (eQMS)

Microsoft Office

Job description

Iterative Health is a healthcare technology and services company on a mission to advance gastrointestinal care through relentless innovation. With deep expertise in artificial intelligence and clinical research, we empower healthcare professionals to provide consistently high-quality colorectal cancer screenings and support clinical research teams and study sponsors to expand and accelerate patient access to novel therapeutics.

Iterative Health is seeking a Quality Manager. This dynamic, fast-paced role
will require experience with leading QMS initiatives to support the medical
device side of Iterative health and is required to have strong attention to
detail and documentation. A successful candidate will work cross-
functionally with a diverse team of machine learning and hardware/software
engineers, clinical experts, and product managers to solve challenging real-
world scientific problems that have a company-wide impact. The person in
this role will be responsible for the day to day activities associated with the
management all quality department initiatives. Candidates must have a
strong knowledge of the applicable medical device regulations.

Quality Manager Job Responsibilities:
● Ensure compliance with FDA 21 CFR Part 820 , ISO 13485, ISO 14971 and
CFR Part 11 across all quality processes and documentation
● Oversee the electronic quality management system (eQMS), ensuring
full utilization and regulatory alignment
● Manage internal and external audits, CAPAs, complaint handling,
MDRs, and recall readiness
● Serve as QMS subject matter expert (SME) and primary liaison for
internal audits, regulatory inspections, and third-party audits.
● Maintain and improve procedures for configuration management,
including change control, validation, and rollout planning
● Supervise supplier quality, incoming inspection, and calibration
activities, ensuring accurate records and effective controls

● Maintain quality records including the Device Master Record,
labelling files, and training documentation
● Analyze production and field data to identify trends, drive corrective
actions, and support continuous improvement
● Lead continuous improvement initiatives to reduce defects and
enhance product quality and process consistency
● Track and report on quality metrics, audit outcomes, and customer
feedback to inform quality initiatives
● Promote quality and regulatory awareness through training and cross-
functional engagement
Required Skills:
● Experience in a Quality role within a medical device, experience with
SaMD preferred
● Proficiency with electronic quality management systems (eQMS)
● Strong understanding of ISO 13485, ISO 9001, IEC 62304, QSR, and
cGMP regulations
● Working knowledge of Quality System Regulations and global
compliance standards
● Exposure to quality practices in a supply chain or manufacturing
context
● Experience supporting regulatory audits and inspections
● Strong interpersonal and influencing skills across functions
● Detail-oriented with a proactive approach to problem-solving
● Solid computer literacy, including Microsoft Office application
● Ability to work effectively in a regulated, fast-paced environment
Education and Experience Requirements
● A bachelor’s degree with a minimum of 5 years of experience in the
field

● Lesser degree with more experience considered

Some of our benefits include:

• Vision/Dental/ Medical Insurance
• Life/Disability Insurance
• Stock Options
• Flexible Work Hours
• Unlimited Paid Time Off

At Iterative Health, we’re actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact [e-mail].

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