Job Description
About ANGLE:
ANGLE is a world leading liquid biopsy company with sample-to-answer solutions. ANGLE's proven patent protected circulating tumor cell (CTC) harvesting technology is known as the Parsortix® system. ANGLE's Parsortix® system is FDA cleared for its intended use in metastatic breast cancer and is currently the first and only FDA cleared medical device to harvest intact circulating cancer cells from blood.
The Parsortix system enables a liquid biopsy (a simple blood test) to be used to provide the circulating metastatic breast cancer cells to the user in a format suitable for multiple types of downstream analyses. The system is based on a microfluidic device that captures cells based on a combination of their size and compressibility. The system is epitope independent and can capture all phenotypes of CTCs (epithelial, mesenchymal and EMTing CTCs) as well as CTC clusters in a viable form (alive). CTCs harvested from the system enable a complete picture of a cancer to be seen; as being an intact cell they allow DNA, RNA and protein analysis as well as cytological and morphological examination and may provide comparable analysis to a tissue biopsy in metastatic breast cancer. Because CTC analysis is a non-invasive process, unlike tissue biopsy, it can be repeated as often as needed. This is important because cancer develops and changes over time and there is a clear medical need for up-to-date information on the status of a patient’s tumor. In addition, the live CTCs harvested by the Parsortix system can be cultured, which offers the potential for testing tumor response to drugs outside the patient.
Join our Team:
This is an exciting time at ANGLE and our team in Guildford are looking for a Scientist 1 to join Product & Technology Development – Engineering department.
At ANGLE, we foster a dynamic, entrepreneurial approach to translating leading edge translational research into clinical diagnostics. We offer the potential for significant corporate growth and career development. We promote a culture of collaboration and shared excellence while encouraging an open and honest exchange of ideas.
We are always in search of potential employees who share our vision and want to make a difference today. In your submission, please describe your background and what you can bring to our team along with attaching your resume.
Principal Accountabilities:
- Hands-on laboratory bench work, primarily in the area of medical device development.
- Provide scientific and technical support to programmes and projects.
- Responsible for on-time and on-budget delivery of work packages within a project, including timely reporting of progress on projects and on metrics to monitor and mitigate risk and to ensure product deadlines are met.
- Responsible for quality and regulatory compliance of work undertaken.
- Independently keep a current knowledge base in relevant areas of scientific and technical research.
- Manage the day to day running of assigned development projects within the Quality Management System (ISO13485:2016) and working to the New Product Development (NPD) operating procedure.
- Undertake additional ad-hoc tasks as required.
Qualifications, Experience, Knowledge and Attributes:
- B.Sc. in either Life Sciences or Engineering.
- Product Development or design of Medical devices experience is essential.
- Basic laboratory skills including but not limited to, pipetting and reagent preparation.
- Experience working to strict quality standards such as Medical Device regulations and standards including, but not limited to, 21 CFR 820, ISO 13485, 93/42/EEC, IVD 98/79 EC, ISO14971, GMP, GLP, QSR.
- A strong understanding of the importance of accurate record keeping within a strictly controlled quality system is essential.
- Manage and deliver product development projects to agreed performance specifications, on time and within budget.
- An eye for detail and commitment to high quality data
- A flexible, can-do approach to the requirements of the job
- Organisational skills and the ability to rapidly prioritise tasks in response to unexpected opportunities or risks.
- Excellent accuracy and attention to detail in practical and written work.
- Strong team player with excellent analytical and interpersonal skills.
- Good report writing skills, with the ability to communicate results to technical and non-technical staff.
- Ability to work independently with minimal supervision.
- Continuous learner with a keen appetite for cross-disciplinary work.
- Entrepreneurial thinking and work ethic.
Important! Due to the nature of the role, our requirement is for this position to be Guildford based, office hours, five days per week.
As a member of our highly skilled and fast-growing team you will receive opportunities for development and a competitive benefits package.
Please let us know if you require disability-related accommodation during the recruitment process so that we can work with you to meet your needs.
Furthermore, please be advised that if you submit an application to us for this position, your application and personal details will be processed in accordance with our Data Privacy Notice for Job Candidates.
Job Type: Full-time
Salary: £30,000.00-£32,000.00 per year
Benefits:
- Bereavement leave
- Company events
- Company pension
- Cycle to work scheme
- Employee discount
- Financial planning services
- Flexitime
- Free parking
- Health & wellbeing programme
- Life insurance
- On-site parking
- Private medical insurance
- Referral programme
- Shuttle service provided
- Sick pay
Schedule:
Work Location: In person
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