6,608 Laboratory Scientist jobs in the United Kingdom
Trainee Laboratory Scientist
Posted today
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Job Description
Outline of Role
To help in all aspects of the laboratory workflow
Responsible for ensuring all calibration checks are performed according to schedule
Following procedures in the:
a. Registering samples
b. Preparation of samples for analysis
- Ensure cleanliness of laboratory by:-
a. general cleaning of laboratory work surfaces, floors, equipment and fridges/freezers when necessary and according to the laboratory cleaning schedule
- Conform to ISO17025 standards by:-
a. following procedures
b. maintaining good cleanliness and safe working practices
c. bringing any quality issues to the attention of the Laboratory Manager
- Informing the Laboratory Manager when new stock is required
Key Responsibilities:
To ensure that all laboratory staff are supported to ensure operations run efficiently to meet customer requirements
To prepare samples for analysis
Ensure the Calibration check schedule is maintained
To assist with relevant laboratory paperwork as directed by Laboratory Scientists and Laboratory Manager
To ensure good working practices across the Laboratory
To maintain a high level of personal and professional development
To ensure that all laboratory operations are in accordance with relevant QC and QA systems and procedures
To assist with administrative duties.
To bring any quality issues to the attention of the Laboratory Manager.
To maintain customer confidentially
At no time to accept any inducement in relation to test results
To undertake any other duties that fall within the spirit of this job description
Performance Expectations
o Work accurately and independently
o Excellent Attention to detail is crucial
o Drive and Maintain industry leading IQC and EQA performance
o An excellent level of customer satisfaction
o Adhere to the Impartiality and Confidentiality Policies set out by PiQ Laboratories Ltd
Essential Qualifications
o Degree or equivalent qualification in relevant scientific subject
o Good customer service skills
o Competent IT skills (e.g. emailing, word processing, data entry systems).
o The capability to write clear and concise documentation.
o Able to learn and assimilate new information and maintain confidentiality at all times
o Good level of written and numerical / data handling skills
o Excellent communication and interpersonal skills including ability to build relationships
o Able to work flexibly as required to ensure business needs are met
o Methodical approach to solving queries
o Good time management skills with the ability to work on own initiative, but understand level of responsibility within the team
o Excellent planning and organisation skills with the ability to prioritise work and manage a number of tasks concurrently
o Be highly motivated demonstrating good initiative and self-confidence
o Have the drive and ability to work calmly under pressure under your own direction or within a small team of professionals
o Strong interpersonal skills with the ability to exercise authority and responsibility where required in a diplomatic manner.
o Willingness to undergo any further training to meet the needs of the company
Desirable Qualifications
o Advanced knowledge of SOP's Risk assessments and COSHH
o Validation of results in one of the above disciplines
o Experience in dealing with ISO 17025 quality management system
Job Types: Full-time, Permanent
Pay: £25,000.00-£25,750.00 per year
Benefits:
- Company pension
- On-site parking
Application question(s):
- Do you have experience working to ISO 17025?
- Are you within 30 miles of Crickhowell?
Education:
- Bachelor's (required)
Experience:
- Laboratory: 1 year (required)
Work Location: In person
Application deadline: 20/10/2025
HCPC Clinical Laboratory Scientist
Posted today
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Job Description
Job title: HCPC registered Clinical Scientist
Reports to: Head of Laboratory
Location: Hybrid / 3 days a week onsite at our Manchester HQ
Contract Type: Full-time, Permanent
Salary & Benefits: Competitive Salary + Benefits Package
About Yourgene Health:
Yourgene Health is a leading integrated technologies and services business, enabling the delivery of genomic medicine. The group works in partnership with global leaders in DNA technology to advance diagnostic science. Our mission to enable scientific advances to positively impact human health remains at the core of our focus. It drives and motivates us to develop class leading products and services to meet our customers’ needs.
Yourgene primarily develops, manufactures, and commercialises simple and accurate molecular diagnostic solutions, for reproductive health, precision medicine and infectious diseases. We have a comprehensive offering of non-invasive prenatal tests (NIPT) NGS workflows that have been built with labs in mind, and clinical prenatal screening services. The IONA® test was the pioneer, the first to market as an IVD product, changing the NIPT screening landscape back in 2015. Continuing to build on our expertise in cell-free DNA, our next generation size selection Ranger® Technology uses machine vision for superior precision. With multiple platforms for a range of clinical and research cfDNA sample preparation applications including NIPT, liquid biopsy, gene synthesis and long fragment recovery.
In addition, we offer a portfolio of screening products in reproductive health, precision medicine and infectious disease including screening assays for cystic fibrosis and DPYD genotyping to prevent chemotoxicity.
Yourgene Genomic Services provides a range of genetic analysis services for our clinical, research and pharma customers to support partners with DNA extractions, biobanking, genotyping, arrays and sequencing workflows (WES and WGS). Yourgene Genomic Services offers a Non-Invasive Prenatal Testing (NIPT) Service, enabling clinics to run their own NIPT service for pregnant women with our prenatal screening tests and service laboratory based in Manchester.
Yourgene Health is part of the Novacyt group of companies and is headquartered in Manchester, UK with facilities in Singapore and Canada.
Our Culture:
Yourgene is a growing, vibrant and exciting place to work, we are looking for committed driven individuals to be part of our next growth journey. Our culture is described by our employee's as collegiate, friendly, professional, innovative, open and fast paced. We have many social and wellbeing initiatives run by our Nova Social and Charity Huddle that keep our sense of community and togetherness alive. At Yourgene we focus on putting values led programmes in place to ensure that we can attract, retain and develop our people. We want our people to have a career with Yourgene and we ensure that they are recognised and rewarded for their achievements and commitment, everyone plays a critical role in our growth journey.
Description of role:
We have an opportunity for a full-time and permanent HCPC registered Clinical Scientist to join our genomic services team based onsite at Manchester Science Park. As a clinical scientist you will lead a team of scientists delivering clinical molecular testing services including a Non-Invasive Prenatal Testing within a ISO15189, CQC accredited lab.
You will use your expertise as a clinical scientist to lead the delivery of NIPT service laboratory ensuring compliance with quality and regulatory requirements. You will lead the development of new clinical services, leading the implementation and validation of new tests, ensuring the delivery of high quality testing services. You will lead the troubleshooting of assays and techniques both existing and in development. To implement laboratory procedures for sample receipt, processing, IQC, analysis, checking, interpretation, preparation of reports (both standard and complex) and reporting of results.
You will supervise more junior members of the team and cultivate an open, continuous improvement culture in the lab. In partnership with others, to be responsible for the accuracy, timeliness and appropriateness of a variety of genetic testing, returning results to ordering clinicians and customers.
Key areas of responsibility:
- To run clinical genetic testing service providing NIPT and other complex genetic tests.
- To supervise junior staff ensuring they are trained and maintain their competence in laboratory methods used to provide clinical tests.
- To develop and implement lab procedures to receive, track and process clinical samples.
- To provide expertise in the clinical interpretation of test results and communication of test results to clinicians.
- To use your expertise as a clinical scientist to assist other departments with the development of leading products and services in precision medicine and reproductive health.
- Conduct all activities in accordance with ISO 15189 and CQC requirements, following our quality management services and promoting a continuous improvement mindset.
- Maintain patient data integrity and regulatory compliance for all projects and documentation, adhering to GDPR, GCLP and HTA regulations.
- Identify and address non-conformities, deviations, and risks associated with laboratory activities.
- Develop study plans/protocols, SOPs, and technical documents, ensuring compliance and approval.
- Stand up new clinical services in accordance with the ISO15189 standards ensuring they assays are robust, verified/validated and offer our service customers state of the art molecular testing.
- Lead internal meetings, audits, and communication with senior management to ensure transparency and alignment.
- Liaise with the Quality Department to maintain correct documentation and SOPs.
- Coordinate service schedules with senior management and project managers to meet business needs.
- Ensure compliance with health and safety regulations, including COSHH systems.
- Stay updated on scientific advancements and industry trends to align with company strategy.
Qualifications, Skills and Abilities:
- BSc in an appropriate biological science
- State Registered Clinical Scientist
- 3+ years’ experience working in a clinical laboratory carrying out molecular genetics testing
- Extensive experience working under ISO 15189 Quality Management System.
- Strong understanding of genetics, NGS, bioinformatics, diagnostics, and precision medicine.
- Experience in Oncology testing, whole genome sequencing and Reproductive Health is desirable.
- Ability to critically analyse and interpret scientific data.
- Ability to concentrate and work under pressure
- Excellent writing, oral communication, and presentation skills.
- Experience working with the selection of suitable bioinformatics and clinical reporting tools preferred.
- Demonstratable knowledge of patient consent, HTA, ethics and GDPR
- Confident communicator who is happy to communicate directly with external customers.
- Experience in the supervision of junior staff
Closing Date:
Sunday 26th October, 2025
Equal opportunities:
Yourgene Health and the Novacyt Group of companies provides equal employment opportunities for all current employees and applicants for employment. This policy means that no one will be discriminated against because of race, religion, creed, color, national origin, nationality, citizenship, ancestry, sex, age, marital status, physical or mental disability, affectional or sexual orientation, gender identity, military or veteran status, genetic predisposing characteristics or any other basis prohibited by law.
Notice to Agency and Search Firm Representatives:
Yourgene Health and the Novacyt Group of companies is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Yourgene Health and Novacyt Group employee by a third party agency and/or search firm without a valid written and signed search agreement, will become the sole property of Yourgene Health and the Novacyt Group of companies. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.
HCPC Clinical Laboratory Scientist
Posted today
Job Viewed
Job Description
Job title: HCPC registered Clinical Scientist
Reports to: Head of Laboratory
Location: Hybrid / 3 days a week onsite at our Manchester HQ
Contract Type: Full-time, Permanent
Salary & Benefits: Competitive Salary + Benefits Package
About Yourgene Health:
Yourgene Health is a leading integrated technologies and services business, enabling the delivery of genomic medicine. The group works in partnership with global leaders in DNA technology to advance diagnostic science. Our mission to enable scientific advances to positively impact human health remains at the core of our focus. It drives and motivates us to develop class leading products and services to meet our customers’ needs.
Yourgene primarily develops, manufactures, and commercialises simple and accurate molecular diagnostic solutions, for reproductive health, precision medicine and infectious diseases. We have a comprehensive offering of non-invasive prenatal tests (NIPT) NGS workflows that have been built with labs in mind, and clinical prenatal screening services. The IONA® test was the pioneer, the first to market as an IVD product, changing the NIPT screening landscape back in 2015. Continuing to build on our expertise in cell-free DNA, our next generation size selection Ranger® Technology uses machine vision for superior precision. With multiple platforms for a range of clinical and research cfDNA sample preparation applications including NIPT, liquid biopsy, gene synthesis and long fragment recovery.
In addition, we offer a portfolio of screening products in reproductive health, precision medicine and infectious disease including screening assays for cystic fibrosis and DPYD genotyping to prevent chemotoxicity.
Yourgene Genomic Services provides a range of genetic analysis services for our clinical, research and pharma customers to support partners with DNA extractions, biobanking, genotyping, arrays and sequencing workflows (WES and WGS). Yourgene Genomic Services offers a Non-Invasive Prenatal Testing (NIPT) Service, enabling clinics to run their own NIPT service for pregnant women with our prenatal screening tests and service laboratory based in Manchester.
Yourgene Health is part of the Novacyt group of companies and is headquartered in Manchester, UK with facilities in Singapore and Canada.
Our Culture:
Yourgene is a growing, vibrant and exciting place to work, we are looking for committed driven individuals to be part of our next growth journey. Our culture is described by our employee's as collegiate, friendly, professional, innovative, open and fast paced. We have many social and wellbeing initiatives run by our Nova Social and Charity Huddle that keep our sense of community and togetherness alive. At Yourgene we focus on putting values led programmes in place to ensure that we can attract, retain and develop our people. We want our people to have a career with Yourgene and we ensure that they are recognised and rewarded for their achievements and commitment, everyone plays a critical role in our growth journey.
Description of role:
We have an opportunity for a full-time and permanent HCPC registered Clinical Scientist to join our genomic services team based onsite at Manchester Science Park. As a clinical scientist you will lead a team of scientists delivering clinical molecular testing services including a Non-Invasive Prenatal Testing within a ISO15189, CQC accredited lab.
You will use your expertise as a clinical scientist to lead the delivery of NIPT service laboratory ensuring compliance with quality and regulatory requirements. You will lead the development of new clinical services, leading the implementation and validation of new tests, ensuring the delivery of high quality testing services. You will lead the troubleshooting of assays and techniques both existing and in development. To implement laboratory procedures for sample receipt, processing, IQC, analysis, checking, interpretation, preparation of reports (both standard and complex) and reporting of results.
You will supervise more junior members of the team and cultivate an open, continuous improvement culture in the lab. In partnership with others, to be responsible for the accuracy, timeliness and appropriateness of a variety of genetic testing, returning results to ordering clinicians and customers.
Key areas of responsibility:
- To run clinical genetic testing service providing NIPT and other complex genetic tests.
- To supervise junior staff ensuring they are trained and maintain their competence in laboratory methods used to provide clinical tests.
- To develop and implement lab procedures to receive, track and process clinical samples.
- To provide expertise in the clinical interpretation of test results and communication of test results to clinicians.
- To use your expertise as a clinical scientist to assist other departments with the development of leading products and services in precision medicine and reproductive health.
- Conduct all activities in accordance with ISO 15189 and CQC requirements, following our quality management services and promoting a continuous improvement mindset.
- Maintain patient data integrity and regulatory compliance for all projects and documentation, adhering to GDPR, GCLP and HTA regulations.
- Identify and address non-conformities, deviations, and risks associated with laboratory activities.
- Develop study plans/protocols, SOPs, and technical documents, ensuring compliance and approval.
- Stand up new clinical services in accordance with the ISO15189 standards ensuring they assays are robust, verified/validated and offer our service customers state of the art molecular testing.
- Lead internal meetings, audits, and communication with senior management to ensure transparency and alignment.
- Liaise with the Quality Department to maintain correct documentation and SOPs.
- Coordinate service schedules with senior management and project managers to meet business needs.
- Ensure compliance with health and safety regulations, including COSHH systems.
- Stay updated on scientific advancements and industry trends to align with company strategy.
Qualifications, Skills and Abilities:
- BSc in an appropriate biological science
- State Registered Clinical Scientist
- 3+ years’ experience working in a clinical laboratory carrying out molecular genetics testing
- Extensive experience working under ISO 15189 Quality Management System.
- Strong understanding of genetics, NGS, bioinformatics, diagnostics, and precision medicine.
- Experience in Oncology testing, whole genome sequencing and Reproductive Health is desirable.
- Ability to critically analyse and interpret scientific data.
- Ability to concentrate and work under pressure
- Excellent writing, oral communication, and presentation skills.
- Experience working with the selection of suitable bioinformatics and clinical reporting tools preferred.
- Demonstratable knowledge of patient consent, HTA, ethics and GDPR
- Confident communicator who is happy to communicate directly with external customers.
- Experience in the supervision of junior staff
Closing Date:
Sunday 26th October, 2025
Equal opportunities:
Yourgene Health and the Novacyt Group of companies provides equal employment opportunities for all current employees and applicants for employment. This policy means that no one will be discriminated against because of race, religion, creed, color, national origin, nationality, citizenship, ancestry, sex, age, marital status, physical or mental disability, affectional or sexual orientation, gender identity, military or veteran status, genetic predisposing characteristics or any other basis prohibited by law.
Notice to Agency and Search Firm Representatives:
Yourgene Health and the Novacyt Group of companies is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Yourgene Health and Novacyt Group employee by a third party agency and/or search firm without a valid written and signed search agreement, will become the sole property of Yourgene Health and the Novacyt Group of companies. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.
Senior Freshwater Macroinvertebrate Laboratory Scientist
Posted 1 day ago
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Job Description
About The Role
Are you passionate about freshwater ecology and the vital role aquatic invertebrates play in understanding environmental health? Do you have a sharp eye for detail, strong taxonomic skills, and the drive to deliver scientific excellence?
APEM are looking for a Senior Freshwater Macroinvertebrate Laboratory Scientist to join our expert team at one of our laboratories in Stockport, Edinburgh, or Letchworth . Our analysts are at the forefront of environmental monitoring—supporting projects for water companies, regulators, and consultancies, from drought permits and pollution assessments to invasive species monitoring.
In this role, you’ll analyse and identify macroinvertebrate samples to APEM’s industry-leading standards, ensuring accuracy, consistency, and efficiency in all analyses. You’ll contribute to high-profile environmental monitoring projects, supervise and support junior staff, and continue developing your own expertise—potentially specialising in specific taxonomic groups. You’ll also have opportunities to get involved in fieldwork, data reporting, and the preparation of tenders and technical documentation.
To be successful in this role, you’ll need:
- At least 5 years’ experience identifying freshwater macroinvertebrates from a range of UK habitats
- An excellent AQC record and ability to work to tight deadlines
- A strong understanding of aquatic ecology and the UK water industry
- The ability to manage workloads effectively and maintain high-quality standards
- An understanding of other types of aquatic biological analysis (e.g. phytoplankton, zooplankton, diatoms)
What helps you stand out:
- Experience identifying macroinvertebrates to mixed taxon/species level
- Specialist knowledge in specific macroinvertebrate groups (e.g. damselflies, dragonflies, INNS species)
- Experience in live bankside analysis or training junior staff
- Understanding of Water Framework Directive methodologies
- Experience contributing to business cases or tenders
At APEM, our people are our greatest asset. We value integrity, quality, collaboration, and forward thinking , and we’re committed to providing an inclusive, flexible workplace where everyone belongs. Whether you’re deepening your taxonomic expertise or mentoring the next generation of freshwater scientists, you’ll have the opportunity to grow, contribute, and make a difference.
You will be offered the chance to work on a variety of projects, many of our employees have worked on projects that have been of personal interest to them. We match this with a commitment to continuous development and learning to support your career. We also offer benefits to look after you, from private medical insurance for all employees, access to mental health first aiders and comprehensive income protection if you cannot work. We also offer superb flexible working options, balancing work with your life.
Next steps
We are focused on creating a diverse and inclusive team. If you can’t tick every box on our job description, then we are still keen to hear from you and are open to supporting your development. That may be working part time or supporting you to gain experience in a specific area – we are a growing company and are able to adapt roles to reflect individual skills.
If you think you have what it takes to join our fast-growing business, then please apply immediately on our website. All we need some basic information and your CV, we will review all applications quickly and will respond to all applications.
About Us
The APEM Group is a global environmental consultancy, we work with a range of clients including large corporations and governments to help them understand and solve a wide variety of environmental projects in the UK and globally. Our successful pioneering work has enabled us to grow and combine forces with other businesses who share our ethos and integrity. At our core, our people are working towards the protection of the environment across the globe.
Senior Medical Laboratory Scientist (Microbiology)
Posted 24 days ago
Job Viewed
Job Description
Responsibilities:
- Perform a wide range of microbiological tests on patient samples, including culture, identification, and susceptibility testing.
- Operate and maintain sophisticated laboratory equipment, such as automated culture systems, mass spectrometers, and PCR platforms.
- Interpret and report test results accurately and efficiently, often under pressure.
- Implement and monitor quality assurance procedures to ensure the highest standards of laboratory practice.
- Troubleshoot technical issues with instrumentation and methodologies, escalating complex problems as needed.
- Participate in the validation of new laboratory tests and technologies.
- Assist in the training and supervision of junior laboratory staff and students.
- Maintain detailed and accurate laboratory records in compliance with regulatory requirements.
- Contribute to the development and implementation of laboratory policies and procedures.
- Ensure a safe working environment by adhering to health and safety regulations.
- Liaise with clinicians and other healthcare professionals regarding test results and interpretation.
- Participate in continuing professional development to stay current with advancements in microbiology.
- Contribute to departmental audits and performance improvement initiatives.
- Manage laboratory inventory and reagents, ensuring adequate stock levels.
- A Bachelor's or Master's degree in Microbiology, Biomedical Science, or a related field.
- HCPC registration (or eligibility to register).
- Significant post-qualification experience working as a Medical Laboratory Scientist in a clinical microbiology setting.
- Demonstrated expertise in diagnostic microbiology techniques, including bacteriology, virology, mycology, and parasitology.
- Proficiency in operating and maintaining a variety of laboratory instruments.
- Strong understanding of quality control, accreditation standards (e.g., UKAS), and health and safety legislation.
- Excellent analytical and problem-solving skills.
- Meticulous attention to detail and a commitment to accuracy.
- Effective communication and interpersonal skills.
- Ability to work independently and as part of a multidisciplinary team.
- Experience in staff supervision or training is advantageous.
- Familiarity with laboratory information management systems (LIMS).
Senior Scientific Research Scientist (Bioinformatics)
Posted 3 days ago
Job Viewed
Job Description
Key Responsibilities:
- Design and execute bioinformatics analyses for large-scale genomics, transcriptomics, proteomics, and metabolomics datasets.
- Develop and implement novel computational tools and algorithms to support research objectives.
- Collaborate with experimental biologists, clinicians, and other researchers to interpret biological data and generate actionable insights.
- Contribute to the conceptualization and design of new research projects and grant proposals.
- Manage bioinformatics workflows and pipelines, ensuring data integrity and reproducibility.
- Stay abreast of the latest advancements in bioinformatics, computational biology, and relevant scientific fields.
- Present research findings at internal meetings and external scientific conferences.
- Mentor junior scientists and contribute to the growth of the research team's computational capabilities.
- Author scientific publications in peer-reviewed journals.
- Ensure compliance with data management best practices and ethical guidelines.
Qualifications:
- PhD in Bioinformatics, Computational Biology, Computer Science, Statistics, or a related quantitative field.
- Minimum of 6 years of post-doctoral research experience in bioinformatics or computational biology.
- Proven track record of leading successful research projects and contributing to high-impact publications.
- Expertise in analysing diverse biological datasets using statistical and machine learning methods.
- Proficiency in programming languages commonly used in bioinformatics (e.g., Python, R, Perl) and experience with bioinformatics software packages and databases.
- Strong understanding of molecular biology principles and experimental techniques.
- Excellent problem-solving, analytical, and critical-thinking skills.
- Outstanding communication and presentation skills, with the ability to articulate complex scientific concepts effectively.
- Experience with high-performance computing environments is a plus.
- Ability to work independently, manage priorities, and collaborate effectively in a remote research setting.
This is an exceptional opportunity for a dedicated scientist to drive innovation in a dynamic and collaborative remote research environment. Our client offers a highly competitive salary, comprehensive benefits, and the chance to contribute to significant scientific breakthroughs.
Principal Scientific Research Scientist (Biotechnology)
Posted 15 days ago
Job Viewed
Job Description
Key Responsibilities:
- Lead the design and execution of ambitious research projects in biotechnology, with a focus on developing novel therapeutics for unmet medical needs.
- Direct and mentor a team of research scientists and technicians, fostering a collaborative and high-performance research environment.
- Develop and implement innovative experimental strategies using advanced molecular biology, genomics, and proteomics techniques.
- Critically analyse complex biological data, interpret results, and draw robust conclusions to guide research direction.
- Contribute to the preparation of grant proposals and secure external funding for research initiatives.
- Publish findings in high-impact peer-reviewed journals and present research at international conferences.
- Collaborate effectively with cross-functional teams, including chemistry, pharmacology, and clinical development departments.
- Ensure compliance with all relevant ethical guidelines, regulatory requirements, and safety protocols within the laboratory.
- Identify emerging scientific trends and technologies relevant to the company's strategic goals.
- Contribute to the intellectual property strategy through patent filings and disclosures.
Qualifications and Skills:
- A Ph.D. in Molecular Biology, Biochemistry, Genetics, Biotechnology, or a closely related life science discipline.
- A minimum of 10 years of post-doctoral research experience in an academic or industrial R&D setting.
- A distinguished track record of publications in leading scientific journals and successful grant acquisition.
- Extensive hands-on experience with advanced techniques such as CRISPR-Cas9, next-generation sequencing (NGS), mammalian cell culture, protein expression and purification, and various assay development platforms.
- Proven experience in leading and managing research projects and scientific teams.
- Strong understanding of drug discovery and development processes.
- Exceptional analytical, critical thinking, and problem-solving skills.
- Excellent written and verbal communication skills, with the ability to present complex scientific information effectively.
- A strategic mindset with the ability to identify and pursue novel research opportunities.
- Experience in bioinformatics and computational biology is advantageous.
This is a fantastic opportunity to make a significant impact on the future of medicine within a leading research organization. If you are a visionary scientist ready to lead groundbreaking discoveries, we want to hear from you.
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Senior Scientific Research Scientist - Genomics
Posted 17 days ago
Job Viewed
Job Description
Your key responsibilities will include:
- Designing and implementing advanced genomic research projects, including Next-Generation Sequencing (NGS) experiments.
- Developing and optimizing protocols for DNA/RNA extraction, library preparation, and sequencing.
- Analyzing large-scale genomic datasets using bioinformatics tools and statistical methods.
- Interpreting genomic data to identify disease markers, understand biological pathways, and drive therapeutic insights.
- Managing and maintaining genomic research infrastructure, including sequencing platforms and bioinformatics pipelines.
- Collaborating with internal and external research groups to foster new scientific partnerships.
- Preparing high-impact research publications for peer-reviewed journals and presenting findings at scientific conferences.
- Mentoring and providing technical guidance to junior scientists and research assistants.
- Ensuring strict adherence to all laboratory safety protocols and ethical guidelines.
- Contributing to the development of grant proposals and securing research funding.
Senior Scientific Research Scientist - Genomics
Posted 22 days ago
Job Viewed
Job Description
Your responsibilities will include designing and conducting complex experiments, analyzing large-scale genomic datasets, and developing innovative research methodologies. You will play a key role in interpreting experimental results, contributing to scientific publications, and presenting findings at conferences. Collaboration is key, and you will work closely with a multidisciplinary team of scientists, bioinformaticians, and clinicians, sharing knowledge and expertise effectively. Staying abreast of the latest advancements in genomics, molecular biology, and bioinformatics is essential.
The ideal candidate will possess a PhD in Genomics, Molecular Biology, Genetics, or a related field, with a strong publication record and extensive experience in experimental design and data analysis. Proven expertise in various genomic technologies (e.g., NGS, qPCR, microarrays) and bioinformatics tools is required. Excellent critical thinking, problem-solving skills, and the ability to manage multiple research projects simultaneously are paramount. Exceptional communication and collaboration skills are necessary to thrive in this remote research environment.
Qualifications:
- PhD in Genomics, Molecular Biology, Genetics, or a related life science discipline.
- Minimum of 5 years of post-doctoral research experience or equivalent industry experience.
- Extensive hands-on experience with Next-Generation Sequencing (NGS) technologies and associated workflows.
- Proficiency in bioinformatics tools and software for genomic data analysis (e.g., R, Python, Bioconductor).
- Strong understanding of molecular biology techniques and genetic principles.
- Proven ability to design, execute, and interpret complex scientific experiments.
- Excellent analytical and problem-solving skills.
- Strong publication record in reputable peer-reviewed journals.
- Excellent written and verbal communication skills for scientific reporting and presentations.
- Ability to work independently and as a collaborative member of a remote research team.
Principal Scientific Research Scientist - Biologics
Posted 24 days ago
Job Viewed
Job Description
Key Responsibilities:
- Lead independent research projects focused on the discovery and development of biologic drugs (e.g., antibodies, proteins, vaccines).
- Design, optimize, and perform complex in vitro and in vivo experiments.
- Analyze and interpret large datasets, employing advanced statistical methods.
- Develop and implement novel assays and technologies for biological research.
- Author high-impact publications in peer-reviewed journals and present findings at international conferences.
- Mentor and guide junior research scientists and postdoctoral fellows.
- Collaborate effectively with cross-functional teams, including medicinal chemistry, pharmacology, and clinical development.
- Contribute to intellectual property generation and patent applications.
- Ensure adherence to all laboratory safety regulations and ethical guidelines.
- Manage research budgets and resources effectively.
- Stay abreast of the latest scientific advancements and competitive landscape in biologics research.
Qualifications:
- PhD in Molecular Biology, Immunology, Biochemistry, or a related life science discipline.
- Minimum of 8 years of post-doctoral research experience in the biopharmaceutical industry or equivalent academic setting, with a strong focus on biologics.
- Demonstrated track record of successfully leading research projects and delivering impactful scientific outcomes.
- Extensive hands-on experience with a wide range of molecular and cellular biology techniques relevant to biologics development.
- Proven expertise in assay development, validation, and characterization of biologic molecules.
- Excellent scientific writing and presentation skills.
- Strong leadership, mentorship, and team collaboration abilities.
- Proficiency in data analysis software (e.g., GraphPad Prism, R).
- Experience with bioinformatics tools is a plus.
- Strong understanding of drug discovery and development processes.
This demanding role requires on-site presence at our state-of-the-art research facilities in Birmingham, West Midlands, UK , to foster intensive collaboration and hands-on experimentation. Our client offers a stimulating research environment, competitive compensation, and opportunities for significant career advancement.