86 Pharmaceutical jobs in London

About the Role  

To be employed in this role you must pass an enhanced safeguarding check. 

Our stores operate 24 hours per day, 7 days per week, with that brings a wide variety of shift patterns – if you're looking for flexible working to fit around your lifestyle, then look no further! We'll work with you on your shifts, but weekend working is a requirement of the role, and we may need to be flexible with your work pattern.   

Our in-store Pharmacies are hugely popular with our customers, and they will expect the same warmth and friendliness they get everywhere else in the store – as well as being confident and relaxed about discussing personal health issues, quickly resolving customer problems and taking customers to the right products. 

You will also be responsible for spending time accurately assembling and processing prescriptions. It will be your responsibility to drive awareness of all the extra services we offer in Pharmacy (e.g., Prescription Collection Service, Medicines Use Reviews etc). You will support the Pharmacist with the delivery and effective record keeping of patient services (blood pressure checks, stop smoking schemes etc). You will develop an understanding of the strict Standard Operating Procedures and work to them as our customers will expect nothing less. You will also be collecting the customer's prescription from their doctor's surgery on their behalf and bringing it to the store ready for collection.

We will help you to become a star Pharmacy colleague - you will complete an accredited course to become a qualified Medicine Counter Assistant within 6 months and you'll then move on to train as a Dispensing Assistant which will complete your pharmacy training. Each step of the way you'll be bringing something extra to our service and moving your career forward. 

About You 

You'll be naturally friendly, highly organised and want to get stuck in, working with your team to deliver great results. You have good computer skills, attention to detail and you communicate well with customers. You love problem solving and you're passionate about helping people and care about giving customers a great healthcare experience, helping them find what they need and having a chat along the way. 

Asda that’s more like it

Apply today by completing an online application… 

Everything you'll love

Alongside a competitive salary, you'll get lots of other great benefits too, including:

• Colleague discount: 15% off your shopping at Asda from day 1 for you and a nominated user
• Discounted rates and special offers on Asda services such as Mobile, Pharmacy, Opticians, Personal Loan, Pet Insurance, Travel Insurance, Travel Money, Tyres, Breakdown Cover
• Wagestream: access to flexible pay, income tracker, financial coaching, exclusive savings account and much more.
• Company pension
• Wellbeing: including 24/7 virtual GP, 24/7 EAP service, as well as access to free counselling, legal, mortgage, cancer and bereavement support
• Asda Allies Inclusion Networks – helping colleagues to make sure everybody is included and that our differences are recognised and celebrated.
• Excellent parental leave policies, including maternity & adoption leave, paternity leave, shared parental leave, neonatal care leave, and support for those doing fertility treatments.
• Colleague recognition programme
• Special offers and discounts across a range of services and activities, from airport parking to theme parks and cinemas.

Bank Clinical Pharmacist | Pharmacy | St Anthony's Hospital | Private Hospital | Flexible Working | Sutton

Spire St Anthony's Hospital has an exciting opportunity for a Bank Clinical Pharmacist to join their dedicated team. This role is ideally suited to someone who is looking for the challenge of delivering a comprehensive pharmacy service as part of a friendly team.
Our pharmacists are an integral part of a patients care plan, so you will have the opportunity to interact with patients across various departments to find out their pharmaceutical requirements, review medication history, current prescriptions and relevant clinical data.
Founded in 1904, Spire St Anthony's Hospital delivers care through skilled and dedicated staff working together. With a completed £27m development investment, we provide very high quality healthcare to patients around Sutton, Epsom, Surrey and South London.
We have six operating theatres coving a wide range of specialities and procedure including Ortho, Gynae and Cardio. There is an ITU department providing care and accommodating more complex patients. We have a number of developmental training courses and progression opportunities available for our ambitious employees.

Duties and responsibilities:

• All our clinical teams are focused on delivering personalised care, and our pharmacists play a key role in treating patients with empathy and compassion
li>You will provide advice and support to consultants, nurses and other clinicians ensuring the safe, appropriate and cost-effective use of medicines throughout the hospital
• Build strong working relationships with colleagues and consultants and to work together to improve patient outcomes.
• Suggest new processes/new equipment to improve health outcomes and increase safety throughout the hospital.
• The majority of your time will be spent on the Ward with patients, talking to, and supporting them with discharge medicines, counselling on side effects, and intake requirements.
• Supporting the onsite Prescribing Resident Doctor
• Dispensary is a minimal part of the position here at the Hospital, and the role is predominantly focused on the Ward patient support.

Who we're looking for:

• Pharmacists educated to degree level.
• Current GPhC registration.
• Hospital experience is essential.
• Excellent communicator as you will interact with patients on the Ward to find out their pharmaceutical requirements.

Benefits
We offer competitive rates to our bank colleagues who work on a flexible basis, often to cover busy periods, sickness or annual leave.

• Bank colleagues are paid weekly
• Access to Spire Healthcare pension Access to Blue Light Card discounts
li>Free uniform
• Free DBS
• Full induction, including mandatory training updates
• Opportunities for further training and progression into permanent posts
• Knowledge, support and guidance through your recruitment journey from Spire's specialist Resourcing Team
• Employer and employee contributory pension with flexible retirement options
• 'Spire for you' reward platform - discount and cashback for over 1000 retailers

Our Values
We are extremely proud of our heritage in private healthcare and of our values as an organisation:

• Driving clinical excellence
• Doing the right thing
• Caring is our passion
• Keeping it simple
• Delivering on our promises
• Succeeding and celebrating together

We commit to our employees well-being through work life balance, on-going development, support and reward.
Spire Healthcare is a leading independent hospital group in the United Kingdom and the largest in terms of revenue. From 39 hospitals and 8 clinics across England, Wales and Scotland, Spire Healthcare provides diagnostics, inpatient, day case and outpatient care.

For further information about this role or for an informal conversation about the range of career options available with Spire please contact Rebecca O'Neill on rebecca.o'
Spire Healthcare are proud to be an equal opportunities employer. We celebrate diversity and are committed to creating an inclusive culture for all. Our people are our difference, it's their dedication, warmth and pursuit of excellence that sets Spire Healthcare apart.

Closing date: In order to streamline our recruitment process, we reserve the right to expire vacancies prior to the advertised closing date once we have received a sufficient number of applications.

Data Quality Assurance Analyst - Finance

Our client, a global leader in the finance industry, is seeking a meticulous and detail-oriented individual, with a demonstratable interest in finance to join their team on a temporary contract until end of Dec 2025 (high possibility of extension) with an immediate start date.

This is a remote role with initial onsite training (1-week) based in the City of London. This is an excellent opportunity for individuals with a keen eye for detail and a passion for maintaining data integrity to contribute to a critical project in the financial industry. Successful applicants will receive world-class training, work in a complex and exciting environment and will have the opportunity to apply for permanent roles within the business.

This position will be responsible for onboarding the Beneficial Ownership Registry data for Sweden. The successful candidate will play a crucial role in in onboarding and ensuring the accuracy of a new dataset.

The ideal applicant should have high level of attention to detail and strong experience in Data Entry & Quality Assurance.

Key Responsibilities:

• Entity Disambiguation: Accurately map holders to holder IDs, managing large amount of data (70,000 to 90,000 mappings), ensuring precision and consistency.
• Quality Assurance: Perform post-processing quality checks on all securities provided by the customer, ensuring data integrity and accuracy.
• Data Management: Assist in the management and organization of the dataset, ensuring all records are accurate and up-to-date.

Key Requirements:

• Previous experience in Data entry and Quality assurance is essential.
• Strong attention to detail, focus on accuracy and precision in data handling is a must.
• Ability to analyze data and identify discrepancies.
• Analytical skills to perform Quality Assurance.
• Ability to manage large volumes of data efficiently.
• Time management.
• Good Communication Skills (Verbal & Written).
• Experience or interest in finance in general.

If you are detail-oriented, experienced in data entry and quality assurance, and ready to contribute to a significant project, we encourage you to apply.

Unfortunately, we are only able to contact applicants who are successful to interview stage.

We are an equal opportunities employer and welcome applicants from all sections of the community, regardless of age, sex, gender (or gender identity), ethnicity, disability, sexual orientation, and transgender status.

Quality Assurance Officer - Pharmaceutical | London | 27,500 + Benefits

Are you a detail-oriented scientist/operator/quality professional looking to grow your career into QA within a thriving pharmaceutical environment? Smart4 Sciences are working exclusively with a UK-based pharmaceutical company specialising in unlicensed medicines to recruit a Quality Assurance Officer . This is a fantastic opportunity for someone with a strong grounding in GMP to take on a varied, impactful QA role in a fast-paced, collaborative setting.

As a Quality Assurance Officer , you will play a critical role in supporting the operational delivery of the QA function, ensuring compliance with MHRA regulations, GMP/GDP standards, and internal quality systems. You will be the primary contact for QA queries and contribute directly to the business's success by maintaining high standards across processes, documentation, and customer-facing interactions.

Key Responsibilities:

• Maintain and develop the QA department to meet strategic business goals.
• Support compliance with GMP and GDP legislation.
• Respond to QA queries and customer issues promptly and professionally.
• Review and author Quality documentation including SOPs, deviations, change controls, complaints, and risk assessments.
• Assist with investigations into product quality and technical customer issues.
• Support document control and archiving processes.
• Respond to MHRA recall alerts, supplier non-compliance checks, and license updates.
• Review supplier and customer documents to support approval processes.

About You:

• Prior experience in within a regulated pharmaceutical environment (MHRA experience highly desirable).
• A degree in a scientific discipline (preferred).
• Knowledge of unlicensed medicines and the pharmaceutical supply chain.
• IT literate with excellent communication and organisation skills.
• Proactive, problem-solving mindset and ability to thrive in a fast-paced setting.

Why Apply?

• Join a growing company making a real difference in patient access to vital medicines.
• Work in a quality-led culture with the opportunity to contribute to system improvements.
• Genuine career development prospects and supportive leadership.

If you're ready to take the next step in your QA career, apply now or contact Gareth Gooley on today for a confidential discussion.

• Leading trial setup activities including protocol implementation, approvals, and site initiation
• Ensuring compliance with UK Clinical Trial Regulations, ICH-GCP, and institutional SOPs
• Acting as the primary liaison between the Trials Unit, participating sites, and Chief Investigator
• Coordinating trial communications, documentation, and progress reporting
• Overseeing data quality, monitoring activities, and safety reporting
• Supporting academic dissemination through presentations and reports to committees and funding bodies

• Degree or equivalent experience in clinical trials or a related field
• Proven experience managing interventional trials, including IMP studies
• In-depth knowledge of UK regulations, GCP, and the Research Governance Framework
• Excellent organisational skills and the ability to manage competing deadlines
• Strong communication skills and experience liaising with multiple stakeholders
• Proficiency with clinical trial management systems and Microsoft Office

• Previous experience working in academic or NHS research settings
• Experience in pharmacovigilance and data management
• Ability to supervise or mentor junior staff
• Commitment to equity, diversity, and inclusion in research

Clinical Pharmacist (Band 7) - West Middlesex Hospital

Job Title: Clinical Pharmacist (Band 7)

Location: West Middlesex Hospital, TW7 6AF

Band: Band 7

Contract Type: Locum

Salary: 26 - 30 per hour

About you:

Are you a highly skilled Clinical Pharmacist (Band 7) seeking a locum position? Medacs Healthcare has an exciting opportunity for a Clinical Pharmacist to join an NHS hospital in West Middlesex Hospital, to support them in providing the highest levels of patient care.

Key Responsibilities:

• Work across various wards, checking prescriptions, ensuring their appropriateness and safety for individual patients.
• Provide advice on medication dosage and form, participate in ward rounds, and collaborate with medical staff.
• Discus treatments with patients, their relatives, community pharmacists, and GPs is also part of the role.

Essential Qualifications:

We are looking for an experienced and highly Clinical Pharmacist (Band 7) with:

• Master's degree in pharmacy (MPharm).
• GPhC registration.
• Previous wards-based experience.
• Minimum 2 years' post-graduate experience.
• 6 months recent NHS experience within the last 3 years.
• Full UK right to work.

Benefits:

• Competitive pay rate: 26 30 per hour.
• Access to Health Assured (mental health and wellbeing support).
• First access to shifts with the ability to block book shifts in advance.
• Comprehensive compliance support.
• Holiday pay, pension scheme, and online CPD training opportunities.

Why Choose Us:

We are a friendly and approachable team committed to finding you locum roles to ensure you enjoy both your work life and your home life. We offer 24/7 support for all our clinicians - we are always here when you need us most.

If you are looking for a locum Clinical Pharmacist (Band 7) role apply today.

How to Apply:

Please apply online using the form below and attach a copy of your up-to-date CV.

Unfortunately, we cannot process applications for candidates who cannot provide evidence of a UK right to work.

We are committed to creating a diverse and inclusive workplace and welcome applications from all backgrounds.

Pharmacy Dispenser Assistant (Band 3)

Job Title: Pharmacy Dispenser Assistant (Band 3)

Location: Isleworth

Band: Band 3

Contract Type: Locum

Salary: 13 - 16 per hour

About you:

Are you a JAC or Wellsky trained Pharmacy Assistant (Band 3) seeking a locum position? Medacs Healthcare has an exciting opportunity for a Pharmacy Assistant to join our NHS client in Isleworth who is competent in labelling and dispensing, to support them in providing the highest levels of patient care.

Key Responsibilities:

• Work across various wards, checking prescriptions, ensuring their appropriateness and safety for individual patients.
• Provide advice on medication dosage and form, participate in ward rounds, and collaborate with medical staff.
• Discus treatments with patients, their relatives, community pharmacists, and GPs is also part of the role.

Essential Qualifications:

We are looking for an experienced and highly Pharmacy Assistant (Band 3) with:

• Previous experience working in inpatient or outpatient setting.
• JAC/Wellsky experience essential.
• Full UK right to work.

Benefits:

• Competitive pay rate: 13 - 16 per hour.
• Access to Health Assured (mental health and wellbeing support).
• First access to shifts with the ability to block book shifts in advance.
• Comprehensive compliance support.
• Holiday pay, pension scheme, and online CPD training opportunities.

Why Choose Us:

We are a friendly and approachable team committed to finding you locum roles to ensure you enjoy both your work life and your home life. We offer 24/7 support for all our clinicians - we are always here when you need us most.

If you are looking for a locum Pharmacy Assistant (Band 3) role apply today.

How to Apply:

Please apply online using the form below and attach a copy of your up-to-date CV.

Unfortunately, we cannot process applications for candidates who cannot provide evidence of a UK right to work.

We are committed to creating a diverse and inclusive workplace and welcome applications from all backgrounds.

Role - QA/RA Senior Specialist

Location - London

Hours 40 hours Monday to Friday 

Salary £50,000 to £60,000

Overview

We are seeking a highly skilled QA/RA Senior Specialist to join our clients team. To succeed in this role, you will bring extensive experience in Quality Assurance and Regulatory Affairs within the Medical Device industry , with a strong command of ISO 13485 , regulatory compliance , and post-market requirements.

You will play a key role in maintaining and improving our Quality Management System (QMS), guiding internal and external audits, and ensuring our products meet applicable regulatory standards throughout their lifecycle.

Key Responsibilities

• Develop, implement, and maintain Quality and Regulatory processes in line with applicable regulations and standards (e.g., ISO 13485, MDR).
li>Drive continuous improvement initiatives within the QMS.
• Collaborate cross-functionally and with the external subcontractors to ensure ongoing regulatory compliance.
• Provide QA/RA support during changes and product lifecycle management.
• Lead risk management activities and oversee post-market surveillance processes.
• Conduct thorough root cause investigations and manage Corrective and Preventive Actions (CAPA).
• Coordinate the preparation and maintenance of technical and regulatory documentation.
• Develop, maintain, and execute internal and external audit plans to ensure audit readiness and compliance.
• Author, review, and update QMS policies, procedures, and work instructions.
• Monitor and implement regulatory updates, ensuring company compliance with evolving standards.
• Ensure SOPs are appropriately established, implemented, and followed across all functions.
• Deliver internal training to enhance regulatory and quality awareness throughout the organization.

Required Experience, Skills & Qualifications

• Proven Quality Assurance experience in the Medical Device sector .
• Bachelor's degree (or higher) in a scientific or engineering discipline.
• In-depth knowledge of ISO 13485 , EU  MDR , and global regulatory requirements.
< i>Demonstrated experience managing internal and external audits, including interaction with regulatory bodies and notified bodies.
• Strong understanding of QMS development, maintenance, and continuous improvement.
• Skilled in compiling and maintaining technical documentation
• Strong analytical, organizational, and communication skills.
• Ability to work independently and collaboratively in a cross-functional environment.

The Ideal Candidate

You are a proactive, detail-oriented QA/RA professional with a passion for maintaining the highest standards of compliance and quality in medical device development. You’re a natural collaborator with excellent communication and problem-solving skills, ready to contribute to continuous improvement across both regulatory and quality initiatives.

Job Title: Clinical Trials Manager

Location: London

Contract: 5 months

Hours: 14.5 hours per week (9-5 Mondays/Tuesday)

Rates: 22.79-23.97 p/h

Job Description

SRG are looking for a clinical trials manager to join a leading higher educations provider based in London. The primary role of the post holder is to set up and support a high quality clinical trial at the CCTU.

Duties and Responsibilities

• To establish and maintain effective management systems for the trial
• To act as the central Trials Unit contact for the Trial
• To work closely with the Chief Investigator, trial and IT staff to ensure the successful management of the Trial.
• Secure all necessary approvals for the trial and participating sites according to the UK regulations including UK Research Governance Framework
• Coordinate the design, printing and distribution of trial documentation
• Develop trial specific documentation that is compliant with the CCTU Policies and Standard Operating Procedures (SOPs) and ensure this is implemented and kept up to date.
• Ensure sites have appropriate training and maintain necessary records.
• Work within budget constraints in liaison with the Project Manager.
• Ensure that good communication is maintained between the CCTU and recruiting centre staff
• Provide updates on the progress of the trial at regular Trial Management Group meetings, to the Independent Data Monitoring and Trial Steering Committees and to the funder as required.
• Monitor the trial sites to assess compliance with the protocol and regulatory requirements.
• Prepare under the guidance of the Clinical Project Manager, the trial specifications for the Database.
• Undertake Risk Assessment of the trial and, with the Clinical Project Manager, propose appropriate mitigations.
• Minute trial related meetings.
• Supervise the data collected and enter data if required.
• Supervise the data cleaning and validation, including querying and chasing missing data in a timely manner.
• Monitor trial recruitment, providing support and motivation to recruiting staff as required.
• Ensure the timely submission and processing of data and documents from sites to the CTU including safety events. Prepare and submit the necessary reports to appropriate regulatory, ethical and other parties (such as submission of safety reports to the Ethics Committee).
• Represent the trial at conferences, meetings and internal unit meetings as appropriate.
• Keep the relevant literature searches up to date.
• Participate in university and the CCTU training and development initiatives.
• Carry out any other comparable tasks as required including being prepared to assist those working on other studies/trials as directed by the Head of Clinical Trial Operations.

Experience and Qualifications

• Degree and/or equivalent experience in Clinical Trials
• Experience of managing a clinical trial
• Experience of managing a trial of an investigational medicinal product
• Comprehensive understanding of UK Clinical Trials Regulations, ICH Good Clinical Practice, the European Directives on Clinical Trials and Good Clinical Practice and the Department of Health's Research Governance Framework
• Experience of monitoring
• Experience of using Pharmacovigilance systems
• Experience of working in an academic or similar institution
• Experience of public speaking and giving presentations
• Experience of data management
• Evidence of ability to set up and maintain effective management system in trials
• Excellent IT skills; MS Office Suite, Trial Databases and other Trial related systems (such as IMP management, Randomisation)
• Excellent communication and interpersonal skills
• A methodical and accurate approach to work with attention to detail
• The ability to make and carry out decisions and know when to confer with colleagues or refer matters onwards
• The ability to work without direct supervision; to manage own workload and display good organisational ability
• Take responsibility for setting and meeting targets for your own work and others
• Ability to evaluate risks inherent in clinical trials and decide those which should be prioritised to ensure that risks are properly managed
• Advanced organisational skills, managing several projects that are often time pressured, concurrently
• Ability to supervise other members of the team, promote good working relationships and resolve difficult situations
• Commitment to and knowledge of advancing equality, diversity and inclusion

Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.