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We are seeking a HCPC-registered Biomedical Scientist to join our Pathology team within South West Acute Hospital, Clinical Biochemistry Department. The successful candidate will work as part of a multidisciplinary laboratory service, delivering high-quality diagnostic testing to support patient care across the Trust.

This is an excellent opportunity to develop your skills within a supportive Trust environment that values professional development, quality, and patient safety. This is a temporary position, initially for 3 months, with the potential for extension. Hours of work - Monday to Friday 9am-5pm on a rota basis and may include evenings and weekends. The rate of pay is £19.78-£31.65 per hour. Candidates must have at least 1 Year's experience in a similar role and be HCPC Registered.

What We Need From You:

• Degree/Diploma in Biomedical Science
• HCPC Registration
• At least 1 year's Post Graduate Clinical Experience

What We Will Offer You:

• Weekly Pay
• A minimum of 28 days paid holiday (pro rata)
• Paid Annual Leave
• Inclusion into our company pension scheme

The Next Steps:

• Contact Jessica Young or Danielle Willis at First Choice Enniskillen
• Send your CV via the link

First Choice is an equal opportunities employer

Job Title: Specialist Biomedical Scientist - Infectious Sciences

Location: Taunton

Salary: 39,959 to 48,117 per annum

Job Type: Permanent, Full Time

Southwest Pathology Services (SPS) is seeking a highly motivated and organised Biomedical Scientist, with HCPC registration and IBMS Specialist Portfolio to join our friendly Infection Science team. Applicants can earn up to 48,117 per annum depending on qualifications and experience and subject to agreement, may be entitled to a 10,000 welcome bonus.

About us:

For over 10 years, SPS has supported healthcare improvement across Somerset. Formed in 2012, Southwest Pathology Services (SPS) is a joint venture between SYNLAB UK & Ireland and Somerset NHS Foundation Trust. The partnership serves a population of around 500,000 and delivers services to the Trust and more than 50 GP practices, delivering on over 11 million tests annually. We hold ISO15189 UKAS accreditation and are an HCPC-approved laboratory for IBMS Registration and Specialist Portfolio training.

SYNLAB has a strong commitment to investment in both people and services. A well-established central 'Hub' laboratory is based in Taunton, supported by Essential Service Laboratories at Musgrove Park Hospital and Yeovil District Hospital to provide urgent testing 24 hours a day, 7 days a week. The laboratory has one of the first new generation Kiestra automated platforms in the UK, with over 40 staff processing 400,000 samples per year.

We'd be able to provide sponsorship to those who meet the eligibility criteria.

About the role

SYNLAB UK & Ireland has a strong track record of working in partnership with the NHS to enhance pathology services through successful joint ventures, including SPS.

You will be based within the Infectious Sciences laboratory (including Bacteriology, Parasitology, Virology, Molecular and Mycology), at the Hub laboratory site in Taunton. There will be a requirement to rotate within all areas, subject to completion of suitable training. The department operates 7 days per week with rota for weekend working, on-call and bank holidays- all these have pay enhancements.

Key responsibilities include:

• To perform and interpret routine and specialist Biomedical investigations autonomously to provide patients results within agreed quality standards of service delivery and turnaround times under the supervision of senior staff.
• Work independently, implement and propose changes to procedures for own work area.
• Act as the lead specialist for a designated area within Infection Sciences, such as Quality Management, Health & Safety, Information Technology, or a specific technical discipline, providing expert oversight, driving service development, and ensuring compliance with relevant standards and policies.
• To continue with personal development through academic and/or practical experience.
• To provide professional leadership and training to Basic Grade, Trainee BMS, Associate Practitioners (equivalent grades) and Medical Laboratory Assistants.
• To maintain the standards of conduct required by the Health Professions Council to practice as a registered Biomedical Scientist.
• To provide technical advice to clinicians as to the appropriateness of tests and timescales.
• To assist and carry out duties as directed in Health and Safety, audit, training, incident reporting and quality assurance/quality control
• Together with Senior staff help ensure compliance with all policies as required by regulatory directives, accreditation bodies and local management.
• Utilise the laboratory LIMS, Q-Pulse quality monitoring system and other application software according to authorised protocols including assisting in computer data entry in all areas of the laboratory, document review, non-conformance review and quality assurance processes.
• Communicate efficiently, courteously and with clarity at all times, whether face to face, telephone or electronic methods referring enquiries to senior staff where appropriate. Matters being communicated may include complex information and/or results.
• Demonstrate on going competency against training plans and participate positively in CPD (continuous professional development) activities.

About you:

Qualifications:

• BSc Degree, accredited by the Healthcare Professions Council and IBMS.
• HCPC Registration
• Specialist Portfolio in Microbiology or equivalent experience prior to specialist portfolio release.

What we offer:

• All staff commencing on SYNLAB Hospital terms and conditions are subject to a 3-month probationary period and may be entitled to a welcome bonus of 10,000.
• We offer a comprehensive training budget to support career development, providing the resources and opportunities needed for professional growth.
• SPS promotes continuous professional development through regular seminars, and as part of HCPC registration, staff are expected to maintain an up-to-date CPD portfolio.
• There is a healthy training budget to allow local/distant attendance at Congress/seminars/symposiums.

Please click on the APPLY button to send your CV and Cover Letter for this role.

Candidates with experience of; Biomedical Scientist, Senior Biomedical Scientist, Clinical Scientist, Medical Laboratory Scientist, Laboratory Scientist, Specialist Clinical Scientist will also be considered for this role.

INDEEDH2F

Job Title: Specialist Biomedical Scientist - Infectious Sciences

Location: Taunton

Salary: £39,959 to £48,117 per annum

Job Type: Permanent, Full Time

Southwest Pathology Services (SPS) is seeking a highly motivated and organised Biomedical Scientist, with HCPC registration and IBMS Specialist Portfolio to join our friendly Infection Science team click apply for full job details

Principal Scientist - Analytical

Overview

A global pharmaceutical organisation are seeking a Principal Scientist to join their analytical development team in a state-of-the-art facility supporting cutting-edge API development.

This is an excellent opportunity for an individual looking to advance their career in analytical chemistry with broad responsibilties across AD, project management and commercial activites.

Responsibilities

• Collaborate with cross-functional teams to support drug substance process research and development.
• Develop and implement innovative analytical strategies to enhance operational efficiency and deliver high-quality results.
• Ensure compliance with industry standards, regulations, and company policies specific to analytical methodologies and practices.
• Provide scientific leadership and mentorship to team members, fostering a culture of technical excellence and continuous learning.
• Analyse complex datasets and generate comprehensive reports to support decision-making processes.
• Identify opportunities for growth, innovation, and process improvement within the analytical sciences space.

Qualifications

• Proven experience as a Principal Scientist or in a similar scientific role, demonstrating a strong track record of success in analytical sciences.
• Strong expertise in analytical techniques, problem-solving, and method development.
• Excellent communication, leadership, and collaboration skills.
• Ability to independently manage complex projects and collaborate effectively with multidisciplinary teams.
• Proficiency in advanced analytical tools and relevant software.
• A degree (PhD preferred) in chemistry, biochemistry, analytical sciences, or a related field is required.

Benefits

• Competitive salary of up to 57K.
• Opportunities for professional development and career progression in advanced analytical sciences.
• A supportive and inclusive work environment that values innovation and excellence.
• Access to a state-of-the-art facility equipped with the latest technology to facilitate your work.
• Comprehensive benefits package, including pension contributions and health coverage.
• Flexible working arrangements to promote work-life balance.

If you are an experienced and results-driven professional specialising in analytical sciences, we encourage you to apply for this exciting opportunity. Join us to contribute your expertise, work in a modern research environment, and take the next significant step in your career.

Job Advertisement: Method Development Scientist - Immunoassay

Overview

A leading bioanalytical lab is seeking an immunoassay scientist with expertise in running and developing ligand-binding assays to support client GLP / GCP Bioanalytical studies.

Responsibilities

• Develop and transfer ligand binding assays with support from trained staff.
• Communicate project updates and address client queries.
• Collaborate with Study Directors and operational teams to meet project timelines.
• Ensure seamless transition of methods into validation with internal teams.
• Troubleshoot and resolve assay-related technical challenges.
• Draft and review Analytical Laboratory Methods (ALMs) and Standard Operating Procedures (SOPs).
• Ensure compliance with regulatory requirements during assay development.

Qualifications

• Degree in a relevant scientific field.
• 1+ year of industry experience in ligand binding assay development.
• Strong scientific problem-solving and data interpretation skills.
• Proven ability to explain complex concepts to clients.
• Excellent written and verbal communication skills with high attention to detail.
• Effective task prioritisation and multi-responsibility management.
• Proactive, independent, and reliable work ethic.

Day-to-Day Responsibilities

• Design and execute method development and transfer experiments.
• Collaborate with internal and external stakeholders to meet milestones.
• Troubleshoot assay development challenges.
• Prepare and review relevant documentation.
• Participate in team meetings to discuss progress and resolve obstacles.
• Stay updated on and ensure compliance with regulatory guidelines.

Benefits

• Work with cutting-edge bioanalytical technology.
• Opportunities for professional growth and training.
• Collaborative and inclusive workplace culture.
• Competitive salary and benefits package.

If you're passionate about advancing drug development and meet the qualifications, we encourage you to apply and make a global impact in pharmaceutical research.

Talentmark are recruiting for a Clinical Research Scientist to join a company in the pharmaceutical industry on a contract basis for 12 months. This role is hybrid based, up to 3 days per week in Burgess Hill.

Company:
Our client is one of the world's premier innovative biopharmaceutical companies, discovering, developing and providing over 160 different medicines, vaccines and consumer healthcare products to help improve the lives of millions of people in the UK and around the world every year.

Salary:
Up to 250 per day PAYE or up to 331 per day Umbrella.

Clinical Research Scientist Role:

• Work on the clinical development strategy for large studies and programs in cardiovascular and metabolic diseases.
• Work with Global Regulatory Affairs on regulatory filings and review clinical documents for international submissions.
• Act as the medical lead with health authorities and build relationships with international Key Opinion Leaders.
• Oversee communication strategies for clinical studies and represent the organisation at medical congresses and advisory boards.
• Drive competitive differentiation and innovation, and help shape intellectual property strategies.
• Coach and mentor team members to help them build their skills and confidence.

• You hold an advanced degree, with experience in cardiology, metabolic diseases, obesity or a related field.
• You have experience in academia, diagnostics, or the pharmaceutical industry in the cardiovascular and metabolic diseases area.
• You have a proven track record managing In Vitro Diagnostics or Medical Device studies across all stages of global clinical trials.
• You have led large, complex development programs and guided cross-functional, matrixed teams.
• You have a strong understanding of global standards and regulations such as ICH-GCP, IVDD/IVDR, MDR, FDA, and NMPA.
• You are willing to travel up to 25% depending on project phases.

Asbestos and Exposure Measurement Scientist

Permanent

Based near Buxton, and some WFH

Monday to Friday.

47,686 - 54,453 plus generous Civil Service Pension

Initially the role is Project based, but will become research based.

Our client is seeking a Senior Scientist to deliver asbestos-related site investigations,

research and regulatory support activities across Great Britain.

Working within the Science and Research Centre in Buxton, you will use your asbestos knowledge and practical site experience to support the evidence base underpinning the Control of Asbestos Regulations and help improve the management of asbestos risks in workplaces across Great Britain.

We are particularly interested in candidates with practical experience of asbestos

surveys, duty-to-manage activities and clearance testing.

As a Senior Scientist, you will apply your asbestos expertise to support the regulatory,

forensic, incident investigations and research activities.

For the foreseeable future, a significant proportion of the role will involve external site-

based project delivery activities across Great Britain.

This role involves working with asbestos in both controlled laboratory environments and

during site-based activities. You will be required to wear close-fitting respiratory

protective equipment (RPE) when carrying out certain tasks and must therefore be able

to successfully complete face-fit testing.

Person:

Must be degree level educated.

Practical experience of asbestos surveys, duty-to-manage activities and clearance testing are essential to for the role.

The BOHS Certificate of Competence in Asbestos or a combination of recognised

asbestos qualifications and professional experience that demonstrates equivalent

competence in asbestos surveying, duty-to-manage activities and clearance testing.

Preclinical In-Vitro Toxicology Scientist up to c£70k + Bonus + Benefits

Hampshire, Full Time ABJ6761

ONSITE - 5 days

An exciting opportunity has arisen for an experienced In-Vitro Regulatory Toxicology Scientist to join a leading scientific research and product development organisation focused on in-vitro and pre-clinical assessment. This is an excellent opportunity for an experienced scientist to take a technically influential role within a multidisciplinary environment, contributing to advanced pre-clinical testing capabilities across in-vitro science, product development and regulatory toxicology.

You will provide technical expertise and scientific direction across in-vitro Regulatory and Genetic Toxicology, supporting pre-clinical research, product development and regulatory programmes. The role will suit an experienced toxicologist with strong hands-on laboratory expertise who can work independently, lead technical activities and collaborate with internal teams and external partners.

Key Responsibilities

• Provide technical expertise in the development and application of in-vitro Regulatory Toxicology approaches.
• Lead and execute in-vitro studies, delivering robust, reliable and scientifically defensible data.
• Develop, optimise and apply Neutral Red, Ames and in-vitro micronucleus assays.
• Apply complex cell culture, exposure techniques and biological testing methodologies to investigate product safety and potential human health effects.
• Interpret experimental findings and bridge in-vitro data with analytical, human-use and clinical information where appropriate.
• Provide technical direction for new testing capabilities, methodologies and assessment strategies.
• Plan and deliver technical work programmes to agreed timescales, quality standards and objectives.
• Collaborate with multidisciplinary teams across Preclinical Science, Analytical Science, Toxicology, Clinical and Product Development.
• Build relationships with external technical partners, CROs, academic groups and specialist consultants.
• Support method transfer, validation and implementation of new technologies.
• Ensure data is generated and managed in line with appropriate quality and regulatory requirements within controlled, quality-assured laboratory environments.
• Contribute to continuous improvement of laboratory methods, processes and scientific capabilities.
• Prepare, author and peer-review scientific reports, technical documentation, regulatory materials, presentations and publications.
• Support external scientific collaborations, including method transfer and inter-laboratory validation.

Experience & Skills Required

• Degree, MSc or PhD in Biological Sciences, Toxicology, Pharmacology, Biomedical Sciences, Cell Biology, Molecular Biology or a related discipline.
• Significant practical experience in in-vitro Regulatory Toxicology, Genetic Toxicology or pre-clinical area.
• Hands-on experience with Neutral Red, Ames and/or in-vitro micronucleus testing.
• Strong experience in complex cell culture, exposure techniques, biological assays and data interpretation.
• Experience developing, optimising, transferring or validating in-vitro testing methodologies.
• Understanding of relevant regulatory toxicology guidelines, including OECD, ECVAM and ICCVAM.
• Experience within a controlled, quality-assured laboratory environment, ideally with GMP, GLP or GxP.
• Ability to assess complex biological datasets using appropriate data analysis, computational or bioinformatics.
• Experience contributing to regulatory submissions, scientific reports, technical documentation or external scientific communications.

Desirable

• Experience in disease modelling, molecular toxicology or adverse outcome pathway frameworks.
• Knowledge of bioinformatics, computational biology or advanced biological data analysis.
• Experience with high-content screening, high-throughput assays or innovative in-vitro platforms.
• Experience managing CROs, suppliers or scientific collaborations.

Benefits: Up to £70k + up to 30% bonus + 20% pension

To Apply: Please contact Alison Basson on (phone number removed) / (phone number removed) or apply quoting ABJ6761 to