Life science consultant Work, Jobs in Penn, Bkm (with Salaries)

Medical Device Regulatory Affairs Specialist
Clinica Engineering Medical Solutions Ltd —Reading
- £3,700 - £4,200 a month
- Full-time
- Engineering
- English
- Databases
Quick apply
5d
Aviation Consultant
Egis —Farnborough
- Business development
- No degree
- Communication skills
- Life insurance
10d
Senior Professional Services Consultant (LIMS)
Clinisys —Woking
- £42,641 - £107,302 a year
- Remote
- Databases
- Travel
- AI
4d
Consultant (German Speaking)
Prescient Healthcare Group —London
- Full-time
- Hybrid work
- Research
- Business development
- Bachelor's degree
Quick apply
Science Tutor 2026
Tutor Doctor Buckinghamshire (aka: Tutor Doctor ABC (squared)) —High Wycombe
- £18 - £25 an hour
- Part-time
- Bachelor's degree
- Business
- School
- Flexible schedule
Quick apply
Managing Consultant - E&U - Data Science
PA Consulting —London
- Full-time
- Hybrid work
- Sales
- Master's degree
- Business development
- Annual leave
Quick apply
4h
Genomic Associate
London Womens Clinic —London
- £35,000 - £37,000 a year
- Full-time
- Microsoft Office
- Databases
- Bachelor's degree
- Health & wellbeing programme
- Annual leave
Quick apply
4d
Associate Director - PMO Manager (Life Sciences Client)
Colliers International EMEA —London
- Full-time
- Hybrid work
- Microsoft Powerpoint
- Microsoft Excel
- Mentoring
Quick apply
3h
Medical Strategy Lead, Oncology-Clinical Development (Centre of Excellence)
IQVIA —Reading
- Full-time
- Remote
- English
- Databases
- Mentoring
- Work from home
Assistant Project Manager
The Natural History Museum —South Kensington
- £40,760 a year
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Outlook
- Employee discount
- Life insurance
1d
Associate Principal / Principal, Clinical Outcome Assessment (COA) Strategy Consulting
IQVIA —Reading
- Full-time
- Hybrid work
- Doctoral degree
- Master's degree
- Business development
Recruitment Consultant
Practicus LTD —Henley on Thames
- £28,000 - £45,000 a year
- Full-time
- Hybrid work
- Sales
- Business development
- Recruiting
- Work from home
Quick apply
5h
Geotechnical or Geoenvironmental Consultant
Stantec —Reading
- Engineering
- Master's degree
- Bachelor's degree
- Annual leave
14d
No7 Advisor
Boots —Marlow
- £16 an hour
- Part-time
- Communication skills
- Employee assistance programme
- Employee discount
7d
Associate Consultant - Data & Analytics
Equifax —London
- Full-time
- Communication skills
- Sick pay
MES Consultant
Infor —Farnborough
- Full-time
- Hybrid work
- Spanish
- English
- Travel
Complex Case and Programme Manager - West London
PA Consulting —London
- Full-time
- Hybrid work
- Microsoft Powerpoint
- Analysis skills
- Travel
- Annual leave
Quick apply
Lead Oracle DBA Consultant
Clinisys —Woking
- Remote
- Team management
- AI
- Leadership
Salmonella Typing Lead (ID 4668)
Animal and Plant Health Agency —New Haw
- £38,795 a year
- Overtime
- Doctoral degree
- Presentation skills
- Bachelor's degree
- Annual leave
- Employee discount
4d
Technical Consultant
Clinisys —Woking
- Remote
- Presentation skills
- Continuous improvement
- Agile
10d

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Medical Device Regulatory Affairs Specialist

Clinica Engineering Medical Solutions Ltd
Reading

Quick apply

Job details

Permanent | Full-time
£3,700 - £4,200 a month
5 days ago

Qualifications

Document control
Record keeping
Labelling
Engineering
Filing
Corrective and preventive actions (CAPA)
English
Complaint handling
Databases
Compliance monitoring
Quality assurance
Risk management
Technical writing
English
Cybersecurity
Document management
Communication skills
ISO 13485
Corporate regulatory compliance oversight

Full job description

About the Role

Clinica Engineering Medical Solutions Ltd is looking for a Medical Device Regulatory Affairs Specialist to join our team at Green Park Business Park in Reading. You will support the registration, regulatory compliance, and ongoing market approval of medical devices and healthcare technology solutions.

This role is suited to a detail-oriented regulatory professional who understands how technical documentation, quality standards, clinical evidence, and regulatory requirements contribute to safe and compliant medical products. You will work closely with engineering, quality assurance, clinical, product development, and commercial teams throughout the product lifecycle.

Key Responsibilities

Prepare, review, and maintain regulatory documentation for medical devices and healthcare technology products.
Support product registrations, licence applications, and regulatory submissions in the United Kingdom and other relevant markets.
Assist with UKCA and CE-marking activities for applicable medical devices.
Maintain technical files, declarations of conformity, product classifications, and supporting documentation.
Review product specifications, labelling, instructions for use, and promotional materials for regulatory compliance.
Monitor changes to medical-device regulations, standards, and regulatory guidance.
Conduct regulatory assessments for product modifications, software updates, and manufacturing changes.
Support post-market surveillance and vigilance reporting activities.
Assist with the investigation and documentation of complaints, adverse events, and field safety issues.
Work with engineering teams to ensure regulatory requirements are considered during product development.
Support internal and external regulatory inspections and quality audits.
Maintain accurate regulatory submission records, approval documents, and compliance databases.
Coordinate with authorised representatives, notified bodies, external consultants, and regulatory authorities.
Contribute to risk-management activities and the preparation of product risk documentation.
Provide regulatory guidance to internal teams regarding new and existing products.

What We Are Looking For

At least 2–4 years of experience in medical-device regulatory affairs, quality assurance, pharmaceutical compliance, or a related field.
Good understanding of United Kingdom medical-device regulations.
Familiarity with UKCA marking, CE marking, and medical-device classification requirements.
Experience preparing or maintaining technical documentation for regulated products.
Knowledge of quality-management systems and regulatory documentation controls.
Understanding of ISO 13485 and medical-device risk-management principles.
Ability to interpret complex regulatory standards and communicate requirements clearly.
Strong written communication and technical documentation skills.
Excellent organisation, accuracy, and attention to detail.
Ability to manage several submissions, documentation projects, and deadlines simultaneously.
Strong written and spoken English.
A degree in biomedical engineering, life sciences, pharmacy, healthcare technology, regulatory affairs, or a related discipline is preferred.

Preferred Skills

Experience working with software as a medical device or digitally connected healthcare products.
Knowledge of ISO 14971 risk-management requirements.
Familiarity with clinical evaluations and post-market clinical follow-up documentation.
Experience supporting regulatory submissions outside the United Kingdom.
Knowledge of European Union Medical Device Regulation requirements.
Familiarity with corrective and preventive action processes.
Experience participating in notified-body, regulatory-authority, or customer audits.
Professional certification or additional training in medical-device regulatory affairs.
Understanding of data-protection and cybersecurity requirements for connected medical devices.

Mindset

You are methodical, responsible, and comfortable working in a highly regulated environment. You understand that incomplete documentation or overlooked regulatory details can affect product approval, patient safety, and commercial operations.

You take ownership of your work, raise potential compliance issues early, and communicate regulatory requirements clearly to both technical and non-technical colleagues. You remain calm under deadlines and balance commercial priorities with the need to maintain high regulatory and ethical standards.

Pay: £3,700.00-£4,200.00 per month

Work Location: In person

Quick apply

Refine Your Search

life science consultant jobs in penn, bkm

Medical Device Regulatory Affairs Specialist

Aviation Consultant

Senior Professional Services Consultant (LIMS)

Consultant (German Speaking)

Science Tutor 2026

Managing Consultant - E&U - Data Science

Genomic Associate

Associate Director - PMO Manager (Life Sciences Client)

Medical Strategy Lead, Oncology-Clinical Development (Centre of Excellence)

Assistant Project Manager

Associate Principal / Principal, Clinical Outcome Assessment (COA) Strategy Consulting

Recruitment Consultant

Geotechnical or Geoenvironmental Consultant

No7 Advisor

Associate Consultant - Data & Analytics

MES Consultant

Complex Case and Programme Manager - West London

Lead Oracle DBA Consultant

Salmonella Typing Lead (ID 4668)

Technical Consultant

I want to receive the latest job alerts for life science consultant in penn, bkm

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