39 Pharmaceutical jobs in the United Kingdom

IQVIA is seeking a scientifically credible and field-based Medical Science Liaison (MSL) to support a pivotal oncology clinical trial across the UK, Ireland, and Belgium. You'll be a key scientific partner to clinical trial sites-engaging with investigators, supporting site activation and enrollment, and facilitating high-quality scientific exchange.
**Key Responsibilities:**
+ Provide field-based medical support to clinical research programs in oncology.
+ Deliver credible, balanced presentations on disease area and investigational therapies to investigators and site staff.
+ Engage with clinical trial sites to understand and help resolve medical barriers to patient recruitment and screening.
+ Collaborate with site management and monitoring teams to support site initiation and engagement.
+ Facilitate compliant scientific exchange with healthcare professionals (HCPs) and key opinion leaders (KOLs).
+ Capture and report field intelligence, including protocol feedback, treatment landscape insights, and competitor activity.
+ Represent the program at scientific meetings, advisory boards, and congresses.
+ Maintain up-to-date knowledge of the disease area, investigational assets, and relevant clinical data.
+ Ensure all activities are conducted in accordance with applicable laws, regulations, and company policies.
**Required Qualifications:**
+ Advanced scientific degree: MD, PhD, PharmD (strongly preferred); master's degree may be considered with relevant experience.
+ Minimum 2 years' experience as an MSL or in a scientific/medical role.
+ Oncology experience is essential, ideally in solid tumors (head & neck, thoracic, or gastrointestinal).
+ Strong understanding of clinical trial operations and site engagement strategies.
+ Fluent in English and ideally one additional language relevant to the territory (e.g., French or Dutch).
+ Right to work in the UK as well as willingness to travel across the UK, Ireland, and Belgium.
+ Valid driver's license.
**Why This Role Matters:**
+ Represent a first-in-class therapeutic approach with a dual mechanism of action.
+ Join a global MSL team deployed across 26 countries.
+ Influence trial success through strategic site engagement and real-time insights.
+ Grow your career in a fast-paced, science-led environment where your expertise matters.
Ready to make a difference in oncology? Apply now and bring your scientific expertise, curiosity, and collaborative spirit to a program that puts patients first and science at the center.
#LI-CES
#LI-CS1
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled

**Work Schedule**
Other
**Environmental Conditions**
Office
**Job Description**
**Senior/CRA - United Kingdom**
PPD, part of Thermo Fisher Scientific are currently hiring for experienced Clinical Research Associates across the UK
At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future.
Our clinical department defines, develops and delivers clinical programmes. Our global Clinical Operations colleagues within our PPD® clinical research services provide end-to-end support for clinical trials from study start up to monitoring through to study close out, across commercial and government contracts. Together, we help clients define and develop clinical programs, minimize delays, and implement high-quality, cost-efficient clinical studies.
PPD Clinical Research Services are currently hiring for experienced CRAs to join our team in the UK across a range of locations.
***Competitive sign-on bonus considered for qualified candidates***
**The CRA:**
+ Performs and coordinates all aspects of the clinical monitoring and site management process.
+ Conducts remote or on-site visits to assess protocol and regulatory compliance and manages required documentation.
+ Acts as a site processes specialist, ensuring that the trial is conducted in accordance with the approved protocol, ICH-GCP guidelines, applicable regulations and SOPs to guarantee subjects rights, well-being and data reliability.
+ Ensures audit readiness.
+ Develops collaborative relationships with investigational sites.
+ Detailed tasks and responsibilities assigned to role are outlined in the task matrix.
**A day in the Life:**
+ Monitors investigator sites with a risk-based monitoring approach applies root cause analysis (RCA), critical thinking and problem-solving skills to identify site processes failure and corrective/preventive actions to bring the site into compliance and decrease risks.
+ Ensures data accuracy through SDR, SDV and CRF review as applicable through on-site and remote monitoring activities.
+ Assess investigational product through physical inventory and records review.
+ Documents observations in reports and letters in a timely manner using approved business writing standards.
+ Brings up observed deficiencies and issues to clinical management expeditiously and follow all issues through to resolution.
+ May need to maintain regular contact between monitoring visits with investigative sites to confirm that the protocol is being followed, that previously identified issues are being resolved and that the data is being recorded in a timely manner.
+ Conducts monitoring tasks in accordance with the approved monitoring plan.
+ Participates in the investigator payment process.
+ Ensures a shared responsibility with other project team members on issues/findings resolution.
+ Investigates and follows-up on findings as applicable
+ Provides trial status tracking and progress update reports to the Clinical Team Manager (CTM) as required.
+ Ensures study systems are updated per agreed study conventions (e.g. Clinical Trial Management System, CTMS).
+ Performs QC check of reports generated from CTMS system where required.
+ Participates in investigator meetings as necessary.
+ Identifies potential investigators in collaboration with the client company to ensure the acceptability of qualified investigative sites. Initiates clinical trial sites according to the relevant procedures to ensure compliance with the protocol and regulatory and ICH GCP obligations, making recommendations where warranted. Ensures trial close out and retrieval of trial materials.
+ Ensures that required essential documents are complete and in place, according to ICH-GCP and applicable regulations. Conducts on-site file reviews as per project specifications.
+ Gives to the project team by assisting in preparation of project publications/tools and sharing ideas/suggestions with team members. Performs additional study tasks as assigned by CTM (e.g. trip report review, newsletter creation, lead CRA team calls etc).
+ Facilitates effective communication between investigative sites, the client company and the PPD project team through written, oral and/or electronic contacts.
+ Responds to company, client and applicable regulatory requirements/audits/inspections.
+ Maintains & completes administrative tasks such as expense reports and timesheets in a timely manner.
+ Gives to other project work and initiatives for process improvement, as required.
**Education and Experience**
+ Bachelor's degree in a life sciences related field or a Registered Nursing certification or equivalent and relevant formal academic / vocational qualification.
+ Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 2+ years as a clinical research monitor).
+ Valid driver's license
+ Full Right to work in the UK
+ Fluency in English language
**Knowledge, Skills, Abilities**
+ Effective clinical monitoring skills
+ Demonstrated understanding of medical/therapeutic area knowledge and medical terminology
+ Excellent understanding and demonstrated application of ICH GCPs, applicable regulations and procedural documents
+ Well-developed critical thinking skills, including but not limited to: critical attitude, in-depth investigation for appropriate root cause analysis and decision-making
+ Ability to handles Risk Based Monitoring concepts and processes
+ Effective oral and written communication skills, with the ability to communicate effectively with medical personnel
+ Ability to maintain customer focus through the utilization of good listening skills, attention to detail and the ability to perceive customers' underlying issues
+ Effective social skills
+ Strong attention to detail
+ Effective organizational and time management skills
+ Ability to remain flexible and adaptable in a wide range of scenarios
+ Ability to work in a team or independently as required
+ Good computer skills: proficient knowledge of Microsoft Office and the ability to learn appropriate software
+ Good presentation skills
Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.
**Apply today! Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

Blue Arrow are currently looking for van drivers to work for one of our pharmaceutical companies in Glasgow.

You would be using a handheld scanner delivering pharmaceuticals to pharmacy's/Hospital or prisons.

This can either be local runs or long distance

Dayshift shifts starting roughly between 0600 - 0700 lasting on average around 9hrs.

Monday to Friday £12.21ph

Saturday £13.58ph

PAYE

Experience with multi drop and using handheld scanner is Preferred

If interested, please call Andy on press 2 for driving division

Blue Arrow is proud to be a Disability Confident Employer and is committed to helping find great work opportunities for great people.

**Regulatory Affairs Manager**
**Abbott Diabetes Care**
**Witney, Oxfordshire**
**Competitive Salary + Excellent Benefits**
Abbott Diabetes Care designs, develops and manufactures leading-edge glucose monitoring systems and test strips for use in both home and hospital settings. Our product portfolio includes Freestyle Libre, a recently launched system that is revolutionising how people with diabetes around the world monitor their glucose levels. We are passionate about doing work that improves the quality of people's lives.
We currently have an opportunity for a Regulatory Affairs Manager to join our team, based in Oxfordshire, supporting the significant manufacturing capacity expansion underway at the Witney site plus other Operational and R&D projects.
**Primary Job Function**
You will set the EU Regulatory Strategy that is well-defined and effective. The strategy sets out innovative solutions to Regulatory Approval so that plans can be set out.
You will oversee the Project Management of regulatory projects, integrating with the US and OUS Regulatory organisation, the R&D organisation and other key functional groups.
**Core Job Responsibilities**
+ Ensures maintenance of strong communication and working relationships with the Alameda RA group and other RA teams globally.
+ Ensures maintenance of strong communication and working relationships with the Clinical Affairs organisation, R&D Development groups and US Project Management.
+ Supports the interface and guidance of any external auditors such as FDA and ISO assessors reviewing Technical Files.
+ Provides leadership on Notified Body strategy and regional/global planning of product registration.
+ Responsible for defining the regulatory strategy for product approvals in EU and region.
+ Each new development project (product) requires a regulatory strategy to be created and maintained.
+ Responsible for supporting RA compliance with site EHS policy and procedures.
+ Responsible for maintaining the effectiveness of the Quality System at the site in accordance with Abbott Corporate requirements and applicable regulations.
+ Excellent communication / negotiating skills for discussions with Notified Bodies and Competent Authorities etc.
**Position Accountability / Scope**
+ Responsible for ensuring that products designed, changed or purchased by ADC in Europe meet the quality and regulatory standards as required by regulatory, quality, Abbott Corporate and national requirements.
+ This position must ensure that the products are registered in the countries as appropriate and ensure compliance to QS Regulations, ISO regulations, etc.
+ Responsible for ensuring that products designed, changed or purchased by ADC in Europe meet the quality and regulatory standards as required by regulatory, quality, Abbott Corporate and national requirements.
**Minimum** **Education**
+ Minimum of a Bachelor's degree or equivalent preferably in a Scientific discipline e.g. Chemistry, life Sciences, Biology.
**Minimum** **Experience/Training Required**
+ Minimum of a bachelor's degree is required to ensure that the jobholder has sufficient technical knowledge to effectively and confidently be the Regulatory Affairs Project Mgr in the EMEA region.
+ Knowledge of regulatory requirements for ISO 13485, EMC, MDD (93/42/EEC), IVDD (98/79/EC), MDR 2017/745 & IVDR 2017/756, and FDA Quality Systems Regulations is essential.
+ Experience within a medical or healthcare manufacturing industry in a regulatory role. The position requires an understanding of the needs of the customer and knowledge of regulations and standards affecting IVDs and MDDs, the regulatory bodies and country regulations that govern ADC products to enable the jobholder to interpret and apply regulations and standards to products and processes.
+ You need to have excellent written and oral communication skills necessary to be able to produce succinct reports and documentation and to effectively communicate with other departments, managers and external regulatory organizations.
+ You need to have the depth of Regulatory knowledge to be able to define a Regulatory Strategy that is well defined and effective. Additionally, the depth of experience is required to ensure that innovative solutions to Regulatory Approval paths can be set out.
An Equal Opportunity Employer
Abbot welcomes and encourages diversity in our workforce.
We provide reasonable accommodation to qualified individuals with disabilities.
To request accommodation, please call or email

At Gilead, we're creating a healthier world for all people. For more than 35 years, we've tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer - working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight against the world's biggest health challenges, and our mission requires collaboration, determination and a relentless drive to make a difference.
Every member of Gilead's team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve our bold ambitions, and we're looking for the next wave of passionate and ambitious people ready to make a direct impact.
We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfil their aspirations. Join Gilead and help create possible, together.
**Job Description**
**POSITION OVERVIEW:**
You will act as the Regional Regulatory Lead on more complex or multiple products, compounds, indications or projects in the assigned therapeutic (TA) area. You will typically be assigned multiple products or projects to lead, manage and oversee simultaneously. You will define the regulatory strategy, plans and objectives for assigned products or projects. You may act as the Global Regulatory Lead for early-stage or other programs. You will lead Regulatory Submissions Teams or other Regulatory Project Teams and represent Global TA Regulatory on cross-functional core and sub-teams. You will typically serve as a Gilead contact to / for regulatory authorities. You will oversee preparation and maintenance of regulatory submissions, regulatory labelling and packaging for assigned products or projects; guiding and advising other colleagues in the thorough and compliant completion of these activities. You will also play a leadership role in ad hoc or special projects that continuously improve or otherwise advance Regulatory Affairs capabilities.
**RESPONSIBILITIES:**
+ As needed, represents Gilead in negotiations with regulatory authorities.
+ Makes significant contributions to the ongoing development and refinement of regulatory strategies, processes, standards, practices, efficiencies and capabilities.
+ Represents Regulatory Affairs and may serve as Regional Lead or Global Regulatory Lead on cross-functional/cross-regional Regulatory Submission Teams. Provides strategic advice and guidance to Regulatory Affairs and cross-functional leaders and teams.
+ May participate on other Sub-teams (e.g., Study Management, Clinical, Nonclinical, Biomarkers) or assign such to other colleagues and oversee and guide their sub-team participation.
+ Defines the regulatory strategy for multiple Gilead products or projects.
+ Proactively identifies regulatory or related risks/issues and develops mitigation and/or contingency plan.
+ Oversees and guides the preparation, compilation, and timely filing of regulatory submissions, which require cross-functional interactions for commercial or investigational product(s). Examples include meeting requests, briefing packages, original Investigational New Drug (IND), IND amendment, and routine submissions (e.g., Development Safety Update Reports / DSURs, Investigator Brochure/ IB updates, etc.).
+ Oversees and approves the authoring of regulatory documents, including meeting requests, Module 1 documents for original IND, etc.
+ Oversees and guides labeling, packaging and associated information updates and maintenance in accordance with the product license for assigned products and markets.
+ Critically reviews documents for submission to regulatory authorities.
+ Provides matrix management and leadership to project teams.
+ Provides accurate and thorough input and recommendations into resource plans required to complete own deliverables. Tracks resources to ensure compliance with agreed resource allocation, including budgets.
+ Ensures own work complies with established practices, policies and processes, and any regulatory or other requirements.
**REQUIREMENTS:**
We are all different, yet we all use our unique contributions to serve patients. Please see the following for the qualifications and skills we seek for this role.
**Rest of World Education & Experience**
BA/BSC or advanced degree in life sciences or related field with significant regulatory experience in the biopharma industry, regulatory agency, clinical research or other related healthcare environment. Experience leading a broad range of regulatory activities and setting the regulatory strategy for biopharmaceutical products.
**Knowledge & Other Requirements**
+ In-depth understanding of U.S. Food & Drug Administration (FDA) and European Medicines Agency (EMA) regulatory requirements and International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH) standards for medicinal products. Understands varying regional or country regulatory requirements for assigned markets.
+ In-depth knowledge of current global and regional trends in biopharmaceutical regulatory affairs. Proven effectiveness applying this knowledge to optimize team deliverables and results.
+ Demonstrates advanced regulatory and business knowledge and advanced analytical abilities, as evidenced by strengths in assessing complex, multidisciplinary data, understanding and effectively advising on its regulatory implications.
+ In-depth knowledge of relevant health authorities (HAs), including people, system, processes and requirements, as evidenced by past effectiveness and successes in conducting HA interactions.
+ Able to represent Gilead to regulatory authorities when managing standard and non-standard negotiations.
+ Thorough knowledge of the drug development process, including all key functions involved in the various stages of drug development from early research through post-marketing.
+ Strong leadership presence with demonstrated ability to lead without authority and influence programs, projects and/or initiatives.
+ Strong interpersonal skills and understanding of team dynamics.
+ Strong communication and organizational skills.
+ Strong negotiation and conflict resolution skills.
+ When needed, ability to travel.
**Equal Employment Opportunity (EEO)**
It is the policy of Gilead Sciences, Inc. and its subsidiaries and affiliates (collectively "Gilead" or the "Company") to recruit select and employ the most qualified persons available for positions throughout the Company. Except if otherwise provided by applicable law, all employment actions relating to issues such as compensation, benefits, transfers, layoffs, returns from layoffs, company-sponsored training, education assistance, social and recreational programs are administered on a non-discriminatory basis (i.e. without regard to protected characteristics or prohibited grounds, which may include an individual's gender, race, color, national origin, ancestry, religion, creed, physical or mental disability, marital status, sexual orientation, medical condition, veteran status, and age, unless such protection is prohibited by federal, state, municipal, provincial, local or other applicable laws). Gilead also prohibits discrimination based on any other characteristics protected by applicable laws.
**For Current Gilead Employees and Contractors:**
Please apply via the Internal Career Opportunities portal in Workday.
Gilead Sciences, Inc. is a biopharmaceutical company that has pursued and achieved breakthroughs in medicine for more than three decades, with the goal of creating a healthier world for all people. The company is committed to advancing innovative medicines to prevent and treat life-threatening diseases, including HIV, viral hepatitis and cancer. Gilead operates in more than 35 countries worldwide, with headquarters in Foster City, California.

Are you an experienced regulatory affairs professional looking for a new opportunity? We are currently seeking a talented **Regulatory Affairs Consultant** to join our dynamic team! This is a client dedicated project, and the role can be office or home based in various European locations.
As the Regulatory Affairs Consultant you will play a vital role in our company's worldwide post-approval regulatory activities, specifically focused on Chemistry, Manufacturing, and Controls (CMC) for biological products.
**Primary Tasks & Responsibilities:**
+ Develop submission strategies and plans for post-approval CMC activities such as variations, renewals, market expansions, and annual reports.
+ Assess change controls and provide regulatory assessments of quality changes in production and quality control.
+ Review study reports from the quality control and production departments to ensure compliance with regulatory requirements.
+ Coordinate submission preparation with various departments including manufacturing, supply chain, quality control and quality assurance, and other regulatory departments and local companies.
+ Write and/or review submission content to ensure alignment with regulatory requirements, specifically related to variations and questions from health authorities.
+ Manage projects within all Regulatory Information Management systems, ensuring the maintenance of worldwide submissions.
+ Identify, escalate, and mitigate risks associated with regulatory procedures and activities.
**Experience and Knowledge Requirements:**
+ University-level education, preferably in Life Sciences, or equivalent by experience.
+ Previous experience in regulatory affairs, particularly related to technical/CMC/quality, within the pharmaceutical industry.
+ Strong understanding of CMC and post-approval regulatory requirements.
+ Experience in writing CMC (technical) sections of regulatory documents such as registration files or variations.
+ Knowledge of biological processes.
+ Background in validation/Quality Assurance/production in the pharmaceutical industry, with experience in preparing regulatory documentation. Understanding of qualification/validation principles.
+ Proficiency in Word, PowerPoint, Excel, and experience with Veeva Vault is valued.
+ Team spirit, flexibility, accountability, and organizational skills.
+ Fluent in English (written and spoken).
#LI-REMOTE
EEO Disclaimer
Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.

Description
Project Kuiper is an initiative to launch a constellation of Low Earth Orbit satellites that will provide low-latency, high-speed broadband connectivity to unserved and underserved communities around the world.
Key job responsibilities
Functions include providing strategic direction and executing in the following areas:
· Working with the technical and systems/RF engineering teams to analyze the potential for harmful interference between Kuiper and other satellite networks (both geostationary and non-geostationary) and terrestrial systems, developing the coordination strategy and mitigation techniques, and negotiating favorable coordination agreements.
· Preparing and managing ITU satellite network filings in conformity with the Radio Regulations and applicable deadlines.
· Executing the coordination strategy and reviewing satellite network filings and preserving coordination rights by commenting on filings within the regulatory deadlines.
·Assist with the global licensing strategy by advancing coordination requirements for Kuiper's system.
· Excellent communication skills with the ability to identify tradeoffs, risks, and opportunities; remove bottlenecks; and establish mechanisms to speed progress.
This position may require access to export-controlled information (ECI) subject to EAR and ITAR. Final employment decision is contingent upon satisfactory completion of export control screenings and obtaining any necessary export licenses or approvals, based on nationality, citizenship, and other factors considered by applicable export control regulations.
A day in the life
The Engineer, International Spectrum Management and Strategy will articulate and execute the strategy for enabling and protecting Kuiper's use of radio frequency spectrum and satellite orbits through the ITU filing, coordination, and notification processes. The ideal candidate has strong experiences with RF simulation tools and knowledge of the applicable Radio Regulations, Rules of Procedure, and ITU-R Recommendation.
About the team
The Global Regulatory Affairs team is responsible for enabling and protecting Kuiper's use of radio frequency spectrum at home and abroad, defining and leading the Project Kuiper regulatory agenda. The Regulatory Affairs team operates worldwide, engaging with the International Telecommunication Union (ITU) and regional organizations, coordinating the use of spectrum with other operators, obtaining licenses for Kuiper services, and promoting safety in space. The Global Regulatory Affairs team is also responsible for domestic licensing and collaborates with associations, government agencies, and other satellite operators in order to advocate for rules and regulations in the best interest of our customers. This team works in close collaboration with the Kuiper technical design teams to optimize for spectrum sharing and customer experience as well as with Amazon's public policy and legal teams to enhance the overall regulatory strategy.
Basic Qualifications
- Experience analyzing dynamic interference from satellite systems and/or other radiocommunication systems
Preferred Qualifications
- Masters Degree in Electrical Engineering or related discipline (telecommunications)
- Experience preparing, managing, and coordinating ITU satellite network filings with other satellite operators internationally in conformity with the Radio Regulations
- Experience with non-geostationary satellite systems
- Experience with satellite systems in the 20/30 GHz bands.
- Experience with Visualyse Professional
- Excellent analytical, problem solving, and communication skills.
Amazon is an equal opportunities employer. We believe passionately that employing a diverse workforce is central to our success. We make recruiting decisions based on your experience and skills. We value your passion to discover, invent, simplify and build. Protecting your privacy and the security of your data is a longstanding top priority for Amazon. Please consult our Privacy Notice ( ) to know more about how we collect, use and transfer the personal data of our candidates.
Amazon is an equal opportunity employer and does not discriminate on the basis of protected veteran status, disability, or other legally protected status.
Our inclusive culture empowers Amazonians to deliver the best results for our customers. If you have a disability and need a workplace accommodation or adjustment during the application and hiring process, including support for the interview or onboarding process, please visit for more information. If the country/region you're applying in isn't listed, please contact your Recruiting Partner.

Band 8a Pharmacists (Locum)– Winter Pressure Support |Lincolnshire

Contract : 01 October 2025 – 31 March 2026 Location : Lincolnshire, On-site only Hours : Monday–Friday, 09:00–17:15 Accommodation : Available via Progress Housing

One of our Lincolnshire Clients are on the lookout for a Band 8a Pharmacist to join their escalation ward team during the critical winter pressure period. This is a high-impact locum opportunity for an experienced hospital pharmacist to step in and make a real difference.

What We’re Looking For:

• Essential : Experience in hospital clinical pharmacy services
• Desirable : Frailty/HCOP experience, prescribing qualifications
• Systems Used : Allocate and EMIS