36 jobs found

Regulatory Affairs Consultant PCD320184 Company Description the organisation (PhD) is a London-based service provider specializing in helping pharmaceutical companies gain marketing authorizations in Europe. Role Description This is a part-time, fully remote, contract role for a Regulatory Consultant with experience in EU food contact legislation At the organisation, you are not a freelancer or have your own consultancy business. The consultant will need to provide advice and perform hands-on w ...

R&D Analytical Scientist £17.49–£18.49 an hour Contractor PCD320193 Job description Job Description: R&D Analytical Scientist Location: Slough Contract Length: 12 months Working Hours: 37.5 hours/week  About the Role This is a fully lab-based position within the R&D Analytics team - Remote working is not available. The successful candidate will support multiple projects in a matrix organizational structure and contribute to analytical development and sample an ...

Quality Assurance Manager PCD300085 The organisation have exclusively partnered with an innovative pharmaceutical company who are driven by their purpose to reimagine how drugs can improve the quality of life of patients with rare diseases. They are a fast growing, agile organisation transforming the lives of patients and care givers through the use of cutting-edge pharmaceutical technologies to translate pioneering science to medicine products. Due to continued growth, we are supporting them with a newly created role, looking for an experience ...

Qualified Person in Sheffield PCD330199 Part-time and Contractor Job Description Qualified Person (QP) Following a successful partnership supporting key hires during a period of expansion and rising product demand, this next phase marks continued growth within the Quality function. The organisation specialises in advanced sterile manufacturing and is seeking QPs who are comfortable being site-based for release activities and can offer flexibility around start times. Due to the complexity of the products, comprehensive training ...

Job Title: Biomedical Scientist - LIMS tester (Band 6/7) PCD300087 Location: West Yorkshire Duration: 6-month contract (ASAP start) Schedule: Monday - Friday, 9:00 AM - 5:00 PM Rate of Pay: £30 - £37 per hour DOE (umbrella equivalent) What You'll Be Doing: As a Biomedical Scientist with extensive experience in Winpath and project management, you will play a crucial role in leading and managing a key project across multiple pathology sites. Your main duties will include: • Managing the testing and implementation of Winpath across two sites, ...

Creative Strategist / Copywriter  Full–time PCD320216 Job description 1. THE OPPORTUNITY Base Salary: €2,400 – €3,600/month (depending on experience & skills). Total Compensation with Performance Bonuses: €4,800 – €8,400/month (or more, depending on performance). 2. WHO WE ARE? We’re one of the fastest-growing health & wellness brands in Europe, with a one-of-a-kind product and proven product market fit. If you want to spend your day writing killer ads (and get rewarded big when they scale)—this is the opportunity. ...

Process Mapping Consultant (Lean Six Sigma) -/enterprise resource planning platform £600a day Contractor PCD300098 Global pharmaceutical company require a process mapping consultant with Lean Sigma skills to work in the Centre of Process Excellence team, this role will help to drive enterprise resource planning platform process design with a view to supporting process excellence initiatives across the business. Partner with business and programme teams to identify high-impact opportunities for process optimisation, develo ...

Senior Clinical Project Manager London Contract Competitive PCD320180 Senior Clinical Project Manager Are you an experienced full service Project Manager in the field of clinical trials who's engaged in addressing the challenges facing the research and development of novel compounds in Oncology. Are you passionate about impacting the health and lives of patients around the world? Do you take a consultative approach to trial management, proving to be a valuable partner in trial operational delivery? In this pivotal role you will have full service oversight f ...

Entry Level - Clinical Research Associate London, United Kingdom Clinical Research Associate PCD320181 Job Summary Our successful Clinical Research Associates possess varied backgrounds in medical and other science-related healthcare fields. Individuals who have succeeded in the CRA role include: Nurses Dieticians Pharmacy Technicians Pharmaceutical/Device Sales Representatives Biotech Engineers PhD/Pharm.D candidates Health and Wellness Coordinators Site Coordinators, Clinical Research Coordinators Research As ...

public healthcare sector Programme Manager PCD330204 Contractor Job Description public healthcare sector Programme Manager - 5-month Contract - Outside of IR35 My Customer is seeking an experienced Programme Manager to lead a range of transformational IT programmes within the public healthcare sector, driving improvements across clinical, operational, and business processes. This is a high-impact role where you will deliver technology-enabled change that enhances patient care, streamlines workflows, and maximis ...

Clinical Project Manager Location: Hybrid Salary: £67,000 to £82,000 per annum Hours: full-time Contract Type: Fixed-Term/Contract PCD330191 About the role: The post is funded by the NIHR to investigate A Low-Cost, Scalable Treatment Strategy For Improving Hypertension Control In Low And Middle-Income Settings The Project Manager is responsible for the operational development, conduct, oversight and completion of clinical trial research projects. Excellent stakeholder management, problem-solving skills, and adherence to Good Cl ...

Senior Medical Writer Full–time PCD320188 Job description EXPERIENCE State both the minimum and the preferred number of years of relevant experience, and describe the essential functions of the job. Relevant Experience Fulfills one of the following: · Up to 6 years of as a medical writer in the pharmaceutical industry. · At least 10 years of medical or scientific writing experience as a primary job responsibility. Clinical Studies · Advanced understanding of the drug development process (discovery to ...

customer relationship management platform Health Cloud Specialist PCD330209 Full-time Job Description Role: customer relationship management platform Health Cloud Specialist Location: United Kingdom - Remote Salary: Up to £122,000- DOE The organisation has partnered with a leading healthcare technology organisation and they are on a mission to transform patient engagement, streamline care coordination, and revolutionise the way health services are delivered through customer relationship management platfor ...

CSV Engineer PCD320185 Sweden / Europe Regulatory & QA – Quality /Full-time /Remote About the Role At the organisation, we develop innovative medical technologies that enhance healthcare outcomes. As a Computer System Validation Engineer, you will execute validation activities for software tools and computer systems used across engineering, manufacturing, operations, and quality. You will ensure validation activities are planned, executed, and documented in compliance with medical device regulations, maintaining validated state for systems in scope while supporting business continuity and audit readiness. More than just ticking compli ...

Senior Systems Engineer, Medical Devices, Electro-mechanical Systems, Risk, Compliance, ISO 13485, COR7121 £62k - £103k a year Full-time PCD330206 Job Description Senior Systems Engineer, Medical Devices, Electro-mechanical Systems, Risk, Compliance, ISO 13485, COR7121 A rare and exciting opportunity has arisen for an experienced Senior Systems Engineer to join a pioneering scientific R&D company that specializes in the development of medical devices. The Role The Senior Systems Engineer will join a multidisciplinary team to lead the develo ...

Senior Clinical Project Manager Slough, UK PCD300083 Premium Remote Friendly Full-time Clinical Research Archiving Quality System Commercialization Electronic Data Capture The organisation is a global full-service CRO dedicated to professional development and providing an excellent work-life balance, with a quality-focused, collaborative “one-team” culture. We are looking for a dynamic person to join our in-house UK team as a Senior Clinical Project Manager. You will work on projects from our varied client base, ranging from small t ...

Head Of Lab Systems And Engineering PCD300088 Overview The organisation (EIT) Oxford's purpose is to have a global impact by fundamentally reimagining the way science and technology translate into end-to-end solutions and delivering these solutions in programmes and platforms that respond to humanity's most challenging problems. The organisation will ensure scientific discoveries and pioneering science are turned into products for the benefit of society that can have high-impact worldwide and, over time, be commercialised to ensure long-term sustainabil ...

Quality Coordinator United Kingdom £72k – £96k a year PCD300231 Position: Quality Coordinator New United Kingdom The organisation (Nasdaq: CMPS) is a biotechnology company dedicated to accelerating patient access to evidence-based innovation in mental health. the organisation is headquartered in London, UK, with offices in New York City in the US. We focus on developing novel treatments that have the potential to improve the lives of those who are suffering with mental health conditions and who are not helped by current treatm ...

Senior Medical Writer PCD330200 Full-time Job Description About the organisation At the organisation we are a progressive health partner, delivering value and outcomes where needed. We pursue innovative science, focussing initially on the areas of greatest potential and then developing solutions where patient need is high, often in rare or under-served disease areas and in life-threatening or life-limiting diseases and conditions. We work directly with patients, doctors and health care professionals on the front line to ensure patient and clinical needs are guiding our development activities at ...

Scientist / Senior Scientist, Manufacturing / stable cell generation, Cell Engineering and CMC  £43K – £72K a year Full–time PCD320194 Job description Independently of geography, the organisation Pharma is committed to upholding key Nordic values. The company has created a culture of straightforward and honest interactions, and its management emphasizes the balance of professional and home life, leading to happier and motivated employees. This motivation is key to meeting the company's bold mission of becoming a ...

Lab Engineer £86k - £108k a year Full-time PCD330203 Job Description We are talking about the kind of difference that has folks naming their pets / park benches / airports after you. Here, you will team up with world-class researchers, scientists, and IT professionals who are collaborating to facilitate industry-leading research that is saving the lives of millions of patients worldwide. Think of it like the Avengers, but with more lab coats and less spandex. Working in the HPC and Storage team, you will be the supe ...

NPI Engineer - Clinical Diagnostics Salary negotiable Cambridge, Cambridgeshire Permanent, full-time PCD330103 NPI Engineer - Clinical Diagnostics The Role This is a great opportunity for an NPI engineer to play a pivotal role in bringing innovative medical devices from concept through to commercial production. You will be at the heart of new product introduction (NPI) activities, working closely with cross-functional teams to ensure seamless product launches. Essential Requirements Ideally around five years in manufacturing th ...

Senior Medical Writer I (Medical Affairs & Medical Education) PCD300086 Overview THE ROLE We're looking for a Senior Medical Writer I. Our SMW1s work as part of our high-performing writing team, stepping up from Medical Writer 2 level to take on more responsibility for projects, supporting clients with scientific knowledge and content development on their assigned accounts, supporting and reviewing work of junior colleagues, and supporting with organic and new business growth. Qualifications WHO ARE YOU • Considerable experience within a medical communications agen ...

CSV Engineer - Glasgow - Circa 50K plus bonus full-time Glasgow, Lanarkshire PCD330196 CSV Engineer - Glasgow - Circa 50K plus bonus The organisation's client, a rapidly growing organisation with bases across the UK and overseas providing life-saving products to people around the globe, is looking to secure the services of a CSV Specialist / Systems Validation Engineer to take ownership of validation activity across multiple regulated systems, working at the intersection of IT, Quality, and Operations. This is a site-based role reporting into the Head of IT ...

Quality Coordinator Location: London Employment Type: Full-time Salary: £72K–£96K a year PCD290096 Role Overview Position: Quality Coordinator New United Kingdom The organisation (Nasdaq: CMPS) is a biotechnology company dedicated to accelerating patient access to evidence-based innovation in mental health. The Company is headquartered in London, UK, with offices in New York City in the US. We focus on developing novel treatments that have the potential to improve the lives of those who are suffering with ment ...

Associate Pharmacovigilance (PVG) Specialist Watford Entry level 43,000 - 72,000 £ / year (est.) PCD330194 At a Glance Tasks: Monitor safety reports and support patient safety initiatives in a collaborative team. Benefits: Flexible working environment with opportunities for professional growth. Why this job: Kickstart your career in pharmacovigilance and make a real impact on patient safety. The organisation: Bachelor’s degree in Life Sciences or related field; attention to detail is key. Other info: Join a passionate team and learn from experienced ...

Associate Clinical Trial Manager (PhD) - Renal Permanent PCD330192 Competitive Job Description The organisation is currently seeking candidates with Renal related PhDs and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our the organisation Clinical Trial Management team. The aCTM will be a part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. Candidate mus ...

Manufacturing Scientist £43k – £72k a year PCD300090 Job highlights Identified by Google from the original job post Responsibilities The organisation is a key technical role supporting external manufacturing operations across international markets The successful candidate will provide expertise in packaging processes and materials, ensure compliance with global standards, and lead or support initiatives such as product launches, tech transfers, and continuous improvement projects You’ll ...

R&D Scientist | United kingdom jobs in pharmaceuticals PCD330207 £43k - £70k a year Full-time Job Description Overview This is an excellent role if you are looking for your first role in the industry or if you are looking to further expand your industry experience and work on some exciting new science! As part of this role, you will be working across cell biology and molecular biology to work on large scale bioprocessing and protein purification. For this position, the organisation is looking fo ...

Principal Biostatistician FSP - Late Phase Oncology PCD330201 Full-time Job Description As a Principal Biostatistician, you are responsible for statistical activities in support of Oncology late phase clinical trials, including study designs, study protocol and analysis plan development, reviewing and interpreting the analysis of study data, and conducting ad hoc and exploratory analyses. • Minimum Work Requirements: • At least 6 years of experience as biostatistician in the Pharmaceutical/Biotechnology industry in cl ...