Advanced Biomedical Scientist Job at Great Western Hospitals NHS Foundation Trust (Swindon)

Senior Scientist – Research Computational Biology Platforms

The ARIA Computational Biology team is seeking a talented and creative computati...

Location

United States , South San Francisco; Boston; Thousand Oaks

Salary:

146404.00 - 198076.00 USD / Year

Amgen

Expiration Date

Until further notice

Requirements

PhD in computational biology, bioinformatics, data science, or a related discipline [and relevant post-doc where applicable]
Master’s degree in computational biology, bioinformatics, data science, or a related discipline and 3 years of relevant research experience
Bachelor’s degree in computational biology, bioinformatics, data science, or a related discipline and 5 years of relevant research experience
Strong programming expertise in Python and R, with proficiency in Linux/Unix environments, cloud computing, HPC, and collaborative development practices (e.g., Git)
Experience developing complex computational tools and visualizations that translate biological insights into actionable strategies
Experience developing and deploying computational tools and pipelines, including use of workflow management systems (e.g., Nextflow), CI/CD practices, and interactive visualization tools (e.g., Shiny/Streamlit)
Strong background in molecular and systems biology
Demonstrated expertise in the analysis and interpretation of single-cell omics data
Experience leveraging and fine-tuning transcriptional foundation models, large language models (LLMs), and biomedical knowledge graphs to advance research objectives
Familiarity with high-value public data resources (e.g., DepMap, Human Cell Atlas, TCGA, GTEx, and Tahoe-100M) used to complement and enhance analyses of internal datasets

Job Responsibility

Developing and applying methods and platforms to discover, prioritize, and validate targets across a broad range of diseases and therapeutic modalities
Designing and building a Precision Targeting Engine that integrates internal and high-value public data into an automated, scalable framework with custom expression analytics across diverse data types and disease areas
Contributing to the design and evolution of Amgen’s preclinical omics data ecosystem in partnership with the Research Informatics team
Evaluating and integrating emerging AI/ML technologies (e.g., biological foundation models), and developing custom research agents to accelerate early pipeline efforts
Partnering with data science and information systems teams to embed tools and analyses developed within ARIA Computational Biology into integrated R&D platforms
Training and mentoring other scientists in the use of advanced research tools and platforms

What we offer

A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
Stock-based long-term incentives
Award-winning time-off plans
Flexible work models where possible

Fulltime

Senior Clinical Scientist

The Senior Clinical Scientist role is suited to scientifically minded candidates...

Location

United States , Salt Lake City

Salary:

Not provided

Blackrock Neurotech

Expiration Date

Until further notice

Requirements

Ph.D. in Neuroscience, Biomedical Engineering, or a related field
Proven expertise in experimental design, data analysis, and scientific communication
Demonstrated experience working across pre-clinical and clinical research settings, with the ability to translate study objectives into executable protocols and comparable datasets across settings
Experience developing and/or executing acute and/or intraoperative electrophysiology studies
Strong analytical skills and proficiency with statistical software and data visualization tools, including analysis of electrophysiology and device performance data
Excellent written and verbal communication skills
Ability to work independently and as part of a collaborative team

Job Responsibility

Lead and manage clinical research projects, collaborating with pre-clinical and multidisciplinary teams, and ensuring alignment with company goals and regulatory requirements
Partner between clinical and pre-clinical teams to develop and execute acute and intraoperative electrophysiology studies, including defining endpoints, coordinating execution workflows, and ensuring high-quality data acquisition
Support and/or coordinate hardware testing in the context of acute/intraoperative clinical studies (e.g., test planning, setup verification, troubleshooting, and structured capture of outcomes to inform development decisions)
Analyze and interpret complex data sets, providing actionable insights to guide BCI development
Collaborate with cross-functional teams, including engineering, regulatory, and clinical affairs, with emphasis on bridging clinical and pre-clinical stakeholders to align study execution and hardware testing needs
Prepare and present scientific reports, publications, and presentations to internal and external stakeholders
Stay current with advancements in neurotechnology and related fields to inform research strategies
Mentor and provide guidance to junior scientists and other team members

Fulltime

Senior Director, Research and Innovation, Advanced Surgery

Baxter’s Advanced Surgery division ($1+B) offers a portfolio of clinically prove...

Location

United States , Deerfield

Salary:

216000.00 - 297000.00 USD / Year

Baxter

Expiration Date

Until further notice

Requirements

Ph.D. or equivalent in Pharmaceutical Sciences, Biomedical Engineering, Bioengineering, Materials Science, Chemistry, or related discipline. Advanced business degree a plus
15+ years of progressive R&D leadership experience in medical devices, drug delivery, or combination product development
Demonstrated expertise in biomaterial implants, drug formulation, delivery technologies, and translational science
Proven track record advancing programs from concept through IND-enabling or equivalent preclinical/early development stages
Experience with regulatory strategy and clinical pathways for drug-device combination products
Strong communication, strategic thinking, and organizational leadership skills
Must possess strong knowledge of scientific disciplines and solid knowledge of related disciplines. Specific knowledge of Oxidized Cellulose, PEG Hydrogels (for tissue sealing and drug delivery), Fibrin Sealants, Gelatin, Collagen, Recombinant drug development, and Synthetic implantable biomaterials is required
Knowledge of quality and general business systems
Must possess strong ability to negotiate for resources and influence others internally and externally
Must be able to set strategic direction for the organization and broadly communicate the vision

Job Responsibility

Define and execute the long-range research and innovation strategy for Advanced Surgery, with a focus on drug/device combination technologies, local drug delivery, biologics, and biomaterials
Identify and prioritize emerging science and technology opportunities in areas such as anti-adhesion, infection prevention, wound healing, hemostasis, tissue regeneration, and controlled drug release
Build and manage a multi-year innovation portfolio that balances internal R&D programs with external partnerships and exploratory research
Provide scientific leadership in the design and development of local and regional drug delivery solutions, including formulation, stability, and release kinetics
Guide preclinical strategy and translational science to enable robust development pathways for drug-device combination products
Partner closely with Regulatory, Clinical, Quality, and CMC functions to ensure alignment with drug development requirements and regulatory frameworks
Lead multidisciplinary teams of scientists and engineers across biomaterials, drug delivery, pharmaceutical sciences, and surgical technologies
Foster a culture of scientific excellence, creativity, and executional rigor
Ensure effective transition of early concepts to product development programs through disciplined stage-gate processes
Establish strategic collaborations with academic centers, startups, and industry partners to accelerate access to emerging technologies and novel drug delivery approaches

What we offer

Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer
medical and dental coverage that start on day one
insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance
Employee Stock Purchase Plan (ESPP)
401(k) Retirement Savings Plan (RSP)
Flexible Spending Accounts

Fulltime

Histopathology Consultant

An excellent opportunity has arisen for a Consultant in Histopathology to join a...

Location

United Kingdom

Salary:

109725.00 - 145478.00 GBP / Year

Remedium Partners

Expiration Date

Until further notice

Requirements

MBBS (or equivalent medical qualification)
Full GMC registration with a licence to practise
FRCPath (or equivalent)
Broad knowledge and experience across histopathology
Proven ability to work effectively in multi-professional teams
Strong organisational, communication, and leadership skills
Commitment to CPD, audit, and clinical governance
Evidence of involvement in postgraduate and undergraduate teaching

Job Responsibility

Reporting of histology and cytology specimens
Macroscopic specimen dissection (including scientist-supervised dissection)
Multidisciplinary team meetings (MDTs)
Frozen section cover and rapid on-site cytology assessment
Contribution to subspecialty services, including pulmonary pathology and at least one other area
Supervise and train postgraduate doctors and specialty trainees within the deanery
Contribute to dedicated teaching sessions and undergraduate teaching in collaboration with regional universities
Support the development of biomedical scientists in specialist reporting and dissection
Engage with audit, CPD, and quality improvement initiatives
Opportunity to contribute to molecular pathology and digital pathology projects

Fulltime

Senior Principal Scientist – Target Discovery & Biology

Amgen’s Target Discovery & Biology (TD&B) organization integrates functional gen...

Location

United States , Thousand Oaks

Salary:

171106.00 - 209556.00 USD / Year

Amgen

Expiration Date

Until further notice

Requirements

Doctorate degree PhD OR PharmD OR MD [and relevant post-doc where applicable] and 3 years of directly related experience
Master’s degree and 6 years of directly related experience
Bachelor’s degree and 8 years of directly related experience
Doctorate degree in cell biology, molecular biology, biomedical engineering, or related discipline
6+ years of relevant experience in biotech or pharma, including leadership of scientific teams
Strong track record in complex in vitro model development, cell engineering, and high-throughput or automated screening
Experience with high-content imaging and transcriptional assay readouts
Demonstrated ability to collaborate with cross-functional teams to translate disease biology into experimental models
Experience with viral vector systems (AAV, lentivirus, or related technologies) for gene delivery and perturbation
Experience in leading or mentoring scientists, with proven success in project execution and team development

Job Responsibility

Provide scientific and operational leadership for a team of scientists delivering advanced in vitro models and screening-ready systems in collaboration with therapeutic area partners
Guide the design, optimization, and screen implementation of cellular models that capture disease-relevant biology, integrating insights from disease tissue profiling data
Champion partnerships with automation colleagues accelerate model deployment and reproducibility
Collaborate with Amgen therapeutic area scientists to define requirements, ensure biological relevance, and deliver systems that enable mechanistic and translational insights
Identify and implement emerging technologies in cell engineering, automation, and complex model systems to enhance the sophistication and throughput of discovery platforms
Foster a collaborative, creative, and scientifically rigorous team culture committed to delivering impact across Amgen’s pipeline

What we offer

A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
Stock-based long-term incentives
Award-winning time-off plans
Flexible work models where possible

Fulltime

Senior Scientist, Device Engineering

Lead the development and launch of drug-device combination products, with a stro...

Location

United States , Waltham

Salary:

115000.00 - 140000.00 USD / Year

Kailera Therapeutics

Expiration Date

Until further notice

Requirements

Minimum of 10+ years of experience in medical device or combination product development, with at least 3 years in a team leadership role
Proven experience with autoinjector, pre-filled syringe, or multidose pen development and launch
Deep understanding of design controls, risk management, human factors, and design transfer
Strong knowledge of applicable regulatory standards and guidance documents
Excellent communication, leadership, and cross-functional collaboration skills
Bachelor’s degree in mechanical engineering, biomedical engineering, or related field with 12+ years of experience. Advanced degree with 10+ years of experience is preferred.

Job Responsibility

Lead the design and development of combination products, including autoinjectors, pre-filled syringes, and multidose pens, from concept through commercialization
Develop device and combination product requirements including user and stakeholder needs, technical requirements, and ensure appropriate engineering translation and subsequent verification and validation of requirements
Oversee and ensure compliance with design controls per FDA and ISO 13485 requirements
Manage risk management activities in accordance with ISO 14971, including hazard analysis, FMEA, and risk mitigation strategies
Drive design verification and validation activities, including test method development, protocol execution, and documentation
Oversee human factors and usability engineering efforts, ensuring compliance with FDA guidance and IEC 62366
Facilitate design transfer to manufacturing, ensuring smooth transition and scalability
Collaborate cross-functionally with clinical, regulatory, commercial, supply chain, and other key functions to ensure integration of device development activities
Author relevant portions of regulatory submissions (INDs, IMPDs, NDAs, BLAs, etc.) for devices and combination product programs
Manage and collaborate with vendors including Contract Design and Manufacturing Organizations (CDMOs), test vendors, and consultants to integrate deliverables into the project Design History File

What we offer

comprehensive health coverage
flexible time off
paid holidays
year-end shutdown
monthly wellness stipend
generous 401(k) match
tuition reimbursement
commuter benefits
disability and life insurance
annual bonus opportunities

Fulltime

IT Data Scientist

Department: 10126 Enterprise Corporate - Enterprise Advanced Analytics. Status: ...

Location

United States

Salary:

51.05 - 76.60 USD / Hour

Advocate Aurora Health

Expiration Date

Until further notice

Requirements

PhD in Data Science, Computer Science, Statistics, Applied Mathematics, Engineering, Biomedical Informatics or a related field, OR a Master’s degree with 2-4 years of applied experience in data science or machine learning
Typically requires 2-4 years of experience in solving complex problems in an analytical environment
Extensive experience working with large-scale structured and unstructured data, ensuring data quality and interpretability
Proficiency in Python and/or R for advanced data analysis, machine learning, and model deployment, along with strong SQL skills for working with large datasets
Expertise in statistical modeling, machine learning, and AI techniques, including regression, classification, time series forecasting, and ensemble methods, with experience in at least some advanced techniques (e.g., Bayesian inference, causal modeling, deep learning, LLMs, NLP, or knowledge engineering)
Demonstrated ability to lead collaborations with stakeholders, define analytics initiatives, and mentor junior team members
Strong critical thinking and problem-solving skills, with an iterative and pragmatic approach to real-world challenges
Proven ability to translate complex data into actionable insights, using storytelling, interactive dashboards, and presentations
Ability to independently manage multiple complex projects, set clear objectives, and drive high-impact initiatives
Experience writing clean, reusable, and well-documented code and working with containerization tools like Docker for model deployment

Job Responsibility

Collaborate with stakeholders and subject matter experts to define and refine data-driven initiatives that enhance healthcare operations and outcomes
Develop a strong understanding of complex, high-volume, and heterogeneous data, ensuring rigorous data development, cleaning, and validation
Apply machine learning and statistical modeling techniques, including regression, classification, clustering, time series forecasting, and ensemble methods
Utilize LLM-based text analytics and NLP techniques to extract insights from unstructured data sources such as clinical notes and reports
Perform exploratory data analysis and build structured analytical workflows using Python, R, and SQL
Communicate findings and methodologies effectively to both technical and non-technical audiences through reports, presentations, and interactive visualizations
Independently manage projects, setting clear objectives, benchmarks, and milestones while balancing iterative development with accountability
Develop well-documented, reusable code on cloud computing platforms to support analytical pipelines
Follow best practices in collaborative software development, including version control (Git) and modular code design

What we offer

Paid Time Off programs
Health and welfare benefits such as medical, dental, vision, life, and Short- and Long-Term Disability
Flexible Spending Accounts for eligible health care and dependent care expenses
Family benefits such as adoption assistance and paid parental leave
Defined contribution retirement plans with employer match and other financial wellness programs
Educational Assistance Program
Premium pay such as shift, on call, and more based on a teammate's job
Incentive pay for select positions
Opportunity for annual increases based on performance

Fulltime

Sr. Program Manager

We are looking for an outstanding individual to join our Program Management grou...

Location

United States , Pleasanton

Salary:

151100.00 - 204500.00 USD / Year

10x Genomics

Expiration Date

Until further notice

Requirements

Bachelor's degree or higher in engineering, chemistry, biology, or a related life science or biomedical engineering field
5+ years proven experience in new product or technology development at a Life Sciences company, with a successful track record (2+ years) as the lead program manager
Demonstrated ability to manage programs spanning both early exploratory research and late-stage development
comfortable with ambiguity early and rigor late
Concrete cases of working with diverse stakeholders — biologists, engineers, chemists, computational scientists — to build shared plans and drive alignment
Demonstrated adoption of advanced AI tools (such as Claude or AI-integrated platforms like Asana or equivalent) as a meaningful part of your day-to-day work
Ability to clearly communicate complex technical topics across various levels of the organization
Strong grasp of technical project management techniques for building and managing project schedules and project costs

Job Responsibility

Serve as Program Manager on 10x R&D teams across new product development and introduction programs, leading cross-functional teams to define and commit to the right scope, schedule, and budget to deliver scientific and business results
Partner closely with technical leads to establish and actively manage program priorities, risks, resources, and schedules — adjusting as the science and development landscape evolves
Drive and track day-to-day program work, ensuring problems are rapidly identified and resolved using modern program management tools and techniques
Lead program communications and phase approval reviews, providing clear and concise updates to all levels of the team and stakeholders, tailoring style to a broad range of audiences
Actively leverage advanced AI tools (e.g., Claude, Gemini, Asana AI) to accelerate program planning, synthesize complex information, and establish best practices for AI-assisted program management across the group
Assess and improve Program Management workflows and communication processes

What we offer

Equity grants
Comprehensive health and retirement benefit programs
Annual bonus program or sales incentive program
Health Package
Easy-to-use Benefits
Family oriented policies like parental leave
Generous Time Off

Fulltime

Advanced Biomedical Scientist

Great Western Hospitals NHS Foundation Trust

Location:
United Kingdom , Swindon

Category:
Health and Beauty

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Nice to have:

Additional Information:

Job Posted:
April 24, 2026

Expiration:
April 30, 2026

Looking for more opportunities? Search for other job offers that match your skills and interests.

Similar Jobs for Advanced Biomedical Scientist