Pharmacy consultant Work, Jobs in England (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
14d
Customer Advisor
Boots —Manchester
- £16 an hour
- Part-time
- In-person
- Employee assistance programme
- Employee discount
Alphega Pharmacy Business Mentor
Alliance Healthcare —Birmingham
- Full-time
- Marketing
- Business development
- Mentoring
Principal Consultant, Senior Director - RWE, Market Access, Regulatory (Europe)
Fortrea —Leeds
- 8 hour shift
- Management
- Doctoral degree
- Research
Associate Consultant – Financial Institutions Consulting - Europe
IQVIA —London
- Full-time
- Hybrid work
- Doctoral degree
- English
- Master's degree
Pharmacy Counter Assistant - Heath & Beauty consultant
Cootes Pharmacy —Finchley
- From £12.71 an hour
- Full-time
- Medication administration
- Inventory control
- Patient care
Quick apply
3d
Pharmacist Information Officer
Great Ormond Street Hospital for Children —London
- £58,133 - £65,261 a year
- Full-time
- Hospital
- Writing skills
- Analysis skills
5d
Health and Wellness Sales Advisor
Boots —Chester
- £16 an hour
- Part-time
- No experience needed
- Communication skills
- Employee assistance programme
- Employee discount
Independent Healthcare Partnerships Consultant
Clinica Vitalis —Nottingham
- Up to £60,000 a year
- Hybrid work
- Sales
- Business development
- Travel
- Work from home
Quick apply
Pharmacy Technician
Kent and Medway Mental Health NHS Trust —Canterbury
- £32,073 - £39,043 a year
- Full-time
- Experience working with children
- Patient care
- Discharge planning
1d
Consultant Neonatologist
The Royal Wolverhampton NHS Trust —Heath Town
- £113,565 - £150,569 a year
- Full-time
- Research
- Paediatrics
- Teaching
1d
Pharmacy Manager (Pharmacist)
Spire Healthcare —Nottingham
- Full-time
- Supervising experience
- Bachelor's degree
- Continuous improvement
- Annual leave
Pharmacy Technician (Bank)
Nuffield Health —Guildford
- Up to £23 an hour
- Part-time
- Computer literacy
- Computer skills
- Communication skills
1d
Patient Administrator
ICON UK —London
- Full-time
- Front desk
- In-person
- Annual leave
- Employee assistance programme
Quick apply
Bank Pharmacy Assistant
Spire Healthcare —Leeds
- Hospital
- English
- Microsoft Office
- Annual leave
Bank Pharmacy Technician
Spire Healthcare —Leeds
- Part-time
- Inventory control
- Hospital
- English
- Annual leave
Pharmacy Manager
Nuffield Health —London
- Full-time
- Management
- Inventory control
- Budgeting
- Gym membership
Customer Service Consultant | Night & Day Shift | Perm | Hybrid
Teladoc Health UK —Brighton
- £27,500 a year
- 8 hour shift
- Hybrid work
- Microsoft Word
- Microsoft Outlook
- Analysis skills
- Health & wellbeing programme
- Annual leave
Quick apply
7d
Rotational/Specialist Rotational Clinical Pharmacist
Northern Care Alliance NHS Foundation Trust —Oldham
- £39,959 - £56,515 a year
- Full-time
- Patient care
- Communication skills
- Annual leave
9d
Locum Pharmacist
Mamedica Dispensary —Basildon
- £30 an hour
- Temporary
- Anatomy knowledge
- Master's degree
- Bachelor's degree
Quick apply
7d

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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
14 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

pharmacy consultant jobs in england

Medical Device Regulatory Affairs Specialist

Customer Advisor

Alphega Pharmacy Business Mentor

Principal Consultant, Senior Director - RWE, Market Access, Regulatory (Europe)

Associate Consultant – Financial Institutions Consulting - Europe

Pharmacy Counter Assistant - Heath & Beauty consultant

Pharmacist Information Officer

Health and Wellness Sales Advisor

Independent Healthcare Partnerships Consultant

Pharmacy Technician

Consultant Neonatologist

Pharmacy Manager (Pharmacist)

Pharmacy Technician (Bank)

Patient Administrator

Bank Pharmacy Assistant

Bank Pharmacy Technician

Pharmacy Manager

Customer Service Consultant | Night & Day Shift | Perm | Hybrid

Rotational/Specialist Rotational Clinical Pharmacist

Locum Pharmacist

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