Pharmaceutical & medical Work, Jobs in Cambridge, Eng (with Salaries)

Medical Device Regulatory and Quality Consultant
PA Consulting —Melbourn
- Full-time
- Annual leave
Pharmacy Homecare Administrator
Royal Papworth Hospital NHS Foundation Trust —Cambridge
- £25,272 - £27,476 a year
- Part-time
- No experience needed
- Microsoft Office
- Maths
11d
Departmental Support Coordinator - Genetic Toxicology
Labcorp —Huntingdon
- Full-time
- Organisational skills
- Communication skills
- Time management
Internal Auditor
BeiGene —Cambridge
- £87,200 - £117,200 a year
- Full-time
- Microsoft Powerpoint
- Microsoft Excel
- Engineering
- Employee stock purchase plan
- Annual leave
9d
R&D Quality Manager
Sandoz —Cambridge
- Full-time
- English
- Project management
- Agile
- Annual leave
Study Coordinator, Toxicology
Labcorp —Huntingdon
- Full-time
- Project management
- Communication skills
3d
Laboratory Support - DMPK
Charles River Laboratories —Saffron Walden
- Weekend availability
- Sales
- Laboratory experience
- Communication skills
- Paid training
- Annual leave
14d
Material Technician – Lab Environment
Avantor —Cambridge
- Full-time
- Laboratory experience
- Bachelor's degree
- Continuous improvement
3d
Quality Assurance Auditor
Labcorp —Huntingdon
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Outlook
2d
Packaging Technologist
Mundipharma —Cambridge
- Full-time
- Continuous improvement
- No degree
- Communication skills
Lab Operations Manager
Avantor —Cambridge
- Full-time
- Management
- Laboratory experience
- Continuous improvement
Medical Director, UK and Ireland
Mundipharma —Cambridge
- Full-time
- English
- Leadership
National Account Manager - North West and Midlands
Alexion Pharmaceuticals,Inc. —Cambridge
- Analysis skills
- AI
4d
Dental Sales Representative
IQVIA —Cambridge
- Full-time
- Sales
- Business development
- Driving
- Employee discount
- Gym membership
General Lab Support, Glasswash Specialist
PerkinElmer —Stevenage
- Customer service
- Organisational skills
- Communication skills
- Annual leave
- Referral programme
10d
Sr Histology Technician
Avantor —Cambridge
- Full-time
- Laboratory experience
- Master's degree
- Bachelor's degree
12d
Programme Lead – Pharmaceutical Drug Delivery Systems
TTP —Cambridge
- Full-time
- Travel
- Communication skills
- Life insurance
Quick apply
Sr Histology Genomics Focused Technician
Avantor —Cambridge
- Full-time
- Laboratory experience
- Bachelor's degree
- No degree
12d
Senior Medical Advisor – Rare Disease & Inflammatory Disease
Amgen —Cambridge
- Leadership
Principal Scientist
Cancer Research UK —Cambridge
- £57,000 - £64,400 a year
- Full-time
- Doctoral degree
- IT
- Communication skills
3d

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Medical Device Regulatory and Quality Consultant

PA Consulting -
Melbourn

Apply Now

Job details

Full-time

Benefits

Cycle to work scheme
Annual leave
Company pension
Private medical insurance

Qualifications

GAMP
Product development
FDA regulations

Full job description

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 diverse teams of 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.

Job description

We are seeking a highly skilled consultant with experience in medical device and/or combination product Quality and Regulatory processes to join our Healthcare & Life Sciences (HLS) consulting team. This role focuses on advising clients on the regulatory, Quality and compliance aspects of medical devices, through a strong understanding of regulatory and quality requirements for medical devices, software as a medical device (SaMD), and/or combination products. The ideal candidate will have experience leading complex technical projects, integrating multidisciplinary expertise, and ensuring regulatory and quality compliance in innovative MedTech and pharmaceutical product developments.

Key Responsibilities:

Regulatory & Quality Compliance for Medical Devices and Combination Products

Provide expertise on global regulatory requirements for medical devices and combination products ensuring compliance with FDA, EMA, MHRA, MDR/IVDR, and ISO standards.
Guide processes for hardware, software, and AI-driven medical device development to ensure compliance with applicable regulatory standards and guidance, including ISO 13485, ISO 14971, IEC 62304, and related standards and guidance for AI-driven medical technologies.
Advise cross-functional teams of designers, mechanical, electrical, software and usability engineers on requirements and best practices for regulatory and quality compliance.
Ensure requirements traceability from user needs through design, development, verification, and validation
Lead risk management activities in accordance with ISO 14971, ensuring safety and efficacy through robust design and process controls.
Develop and optimise clients’ Quality Management Systems (QMS) to streamline compliance and lifecycle management

Stakeholder & Client Engagement

Work closely with clients’ R&D teams, business stakeholders, and notified bodies to align project goals with industry requirements.
Facilitate cross-functional collaboration, ensuring smooth integration between engineering, quality, and regulatory disciplines.
Translate complex technical and regulatory requirements into actionable development strategies for medical technologies.

Flexible working - We are guided by our client work and needs; however, you have autonomy to manage your time and diary to suit your work/life balance.

Qualifications

The ideal candidate will have:
A technical background in Engineering (systems, biomedical, mechanical, electrical, software, or related field) or Applied Science (physics, chemistry, biology, materials science, etc.).
Demonstrated prior direct experience in the design, development, or testing of medical devices and/or combination products.
At least five years' experience in MedTech, pharmaceuticals, or life sciences, with a strong track record in regulated product development.
Deep expertise in regulatory frameworks (FDA, EMA, MDR/IVDR, ISO 13485, IEC 62304, ISO 14971, GAMP, 21 CFR 4/ 820).
Proven ability to work cross-functionally with engineering, quality, and regulatory teams, contributing practical insights from previous technical roles.
Strong problem-solving skills, troubleshooting expertise and the ability to drive technical decision-making in a highly regulated environment ensuring alignment with business and regulatory needs.
Ability to manage multiple concurrent projects.

We know the skill-gap and the ‘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.

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.

We believe diversity fuels ingenuity. Diversity of thought brings exciting perspectives; diversity of experience brings a wealth of knowledge, and diversity of skills brings the tools we need. When we bring people together with diverse backgrounds, identities, and minds, embracing that difference through an inclusive culture where our people thrive; we unleash the power of diversity – bringing ingenuity to life.

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 for you and your family
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
PA share ownership
Tax efficient benefits (cycle to work, give as you earn)

We recruit, retain, reward and develop our people based solely on their abilities and contributions and without reference to their age, background, disability, genetic information, parental or family status, religion or belief, race, ethnicity, nationality, sex, sexual orientation, gender identity (or expression), political belief, veteran status, or by any other range of human difference brought about by identity and experience. We are on a journey towards ensuring our workforce is diverse at all levels and that our firm is representative of the world around us. We welcome applications from underrepresented groups.

Adjustments or accommodations - Should you need any adjustments or accommodations to the recruitment process, at either application or interview, please contact us.

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Refine Your Search

pharmaceutical & medical jobs in cambridge, eng

Medical Device Regulatory and Quality Consultant

Pharmacy Homecare Administrator

Departmental Support Coordinator - Genetic Toxicology

Internal Auditor

R&D Quality Manager

Study Coordinator, Toxicology

Laboratory Support - DMPK

Material Technician – Lab Environment

Quality Assurance Auditor

Packaging Technologist

Lab Operations Manager

Medical Director, UK and Ireland

National Account Manager - North West and Midlands

Dental Sales Representative

General Lab Support, Glasswash Specialist

Sr Histology Technician

Programme Lead – Pharmaceutical Drug Delivery Systems

Sr Histology Genomics Focused Technician

Senior Medical Advisor – Rare Disease & Inflammatory Disease

Principal Scientist

I want to receive the latest job alerts for pharmaceutical & medical in cambridge, eng

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