Medical Device Quality Specialist Consultant

Medical Device Quality Specialist Consultant

We believe in the power of ingenuity to build a positive human future.

As strategies, technologies, and innovation collide, we create opportunity from complexity.

Our teams of interdisciplinary experts combine innovative thinking and breakthrough technologies to progress further, faster. Our clients adapt and transform, and together we achieve enduring results.

We are over 4,000 strategists, innovators, designers, consultants, digital experts, scientists, engineers, and technologists. And we have deep expertise in consumer and manufacturing, defence and security, energy and utilities, financial services, government and public services, health and life sciences, and transport.

Our teams operate globally from offices across the UK, Ireland, US, Nordics, and Netherlands.

PA. Bringing Ingenuity to Life.

• Hybrid working - our approach is to be in the office or on client site a minimum of 2 or 3 days per week. However, the actual time you spend and where you spend it will vary by role or assignment, including up to 5 days per week on a client site.
• This role can be based at either our London Victoria orMelbourn (SG8)office

Within ourLife Scienceswork, we support global organisations to design, develop and bring to market innovative products that improve patient outcomes. This includes complexcombination productsacross pharmaceuticals, medical devices, biologics and advanced therapies.

We are seeking an experiencedMedical Device Quality SpecialistConsultant to support the development and life‑cycle management of Medical Devices (including SaMD) and combination products (drug–device, biologic–device and advanced therapy‑device).

You will play a pivotal role in helping our clients navigate regulatory complexity, embed robust quality systems, and ensure product safety, compliance and performance from early development through to post‑market. Working as part of multi‑disciplinary project teams, you will bring deep technical expertise alongside strong collaboration and stakeholder engagement skills.

What you’ll do

You’ll apply your quality and regulatory expertise across a broad range of client engagements, including:

Quality assurance and compliance

• Working within and advising onQuality Management Systemscompliant withISO 13485, and QMSR.
• Authoring, reviewing and maintainingDesign History Files, risk management file, technical documentation and change control records, ensuring alignment and traceability across the product life cycle.
• Supportingsupplier qualification, audits and gap assessments, ensuring compliance with global regulatory expectations.

Medical Device Expertise

• Medical Devices: Advising on medical device quality and regulatory requirements, including product design and development, risk management, and preparation of technical documentation to ensure US/EU market access and compliance.
• SaMD (Software as a Medical Device): Providing specialised support for Software as a Medical Device, including the implementation and oversight of the software development lifecycle (SDLC) and compliance with IEC 62304 and IEC 82304.
• Combination Products: Knowledge of drug–device or biologic–device combination products, including awareness of regulatory considerations, CCIT (Container Closure Integrity Testing), and stability/compatibility studies, is considered an advantage.

Regulatory and technical strategy

• Interpreting and applying evolvingglobal combination product regulations, providing pragmatic guidance throughout development, technical transfer, commercialisation and post‑market phases.
• Supporting the preparation ofregulatory submissions, technical dossiers and responses to questions from competent authorities and notified bodies.

Technology transfer and lifecycle management

• Leading and supportingtechnology transfer activitiesacross development, scale‑up and commercial manufacturing environments.
• Contributing toprocess validation, equipment qualificationand technical knowledge transfer, ensuring regulatory alignment throughout.

Risk and post‑market activities

• Leadingrisk management activitiesin line withISO 14971, including hazard analysis, risk evaluation and mitigation strategies.
• Supportingpost‑market surveillance, vigilance and complaints investigations, ensuring robust CAPA and documentation.
• Working as part of, or leading,cross‑functional project teams, managing quality deliverables, tracking actions and supporting timely decision‑making.

Qualifications

We’re looking for someone who combines deep technical expertise with a consulting mindset. You’ll ideally bring:

• Prior management consultancy experience is highly desirable
• Adegree in life sciences, pharmacy, engineering, or a related discipline.
• Significant experience (typically8+ years) within medical device industry.
• Strong, hands‑on knowledge ofquality systems and regulatory frameworks(ISO 13485, 21 CFR Part 4, FDA, UK MDR, EU MDR).
• Proven experience authoring and maintainingquality and technical documentationin regulated environments.
• A well‑developed understanding ofrisk management (ISO 14971)and exposure tohuman factors/usability engineering.
• Experience withsupplier quality, audits, CAPA and document control.
• Excellent communication, organisational and project management skills, with the confidence to work with diverse stakeholders.

We know the skill-gap and ‘somewhat need to tick every box’ can get in the way of meeting brilliant candidates, so please don’t hesitate to apply – we’d love to hear from you.

Please be aware that some of our UK roles at PA Consulting require a UK security clearance.

All PA people are required to undergo background checks and to achieve the Baseline Personnel Security Standard however, some UK roles also require higher levels of National Security Vetting, where applicants must have at least 5 years of continuous residency in the UK.

We therefore ask that you only apply if you meet the residency requirements (i.e. you are a British citizen or have been resident in the UK for the past 5 years), as this is the prerequisite for a security clearance. If you're unsure about your eligibility, we encourage you to review the UK Government’s guidance on security vetting before applying.

Additional information

Life At PA encompasses our peoples' experience at PA. It's about how we enrich peoples’ working lives by giving them access to unique people and growth opportunities and purpose led meaningful work.

Our purpose guides how we work with our clients and our teams, and support our communities, to deliver insight and impact, solving the world’s most complex challenges. We're focused on building a workplace that values human difference and diverse mindsets, and a culture of inclusion and equality that unlocks the potential in our people so everyone can be their best self.

We are dedicated to supporting the physical, emotional, social and financial well-being of our people. Check out some of our extensive benefits:

• Health and lifestyle perks accompanying private healthcare
• 25 days annual leave (plus a bonus half day on Christmas Eve) with the opportunity to buy 5 additional days
• Generous company pension scheme
• Opportunity to get involved with community and charity-based initiatives
• Annual performance-based bonus