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- Tasks: Lead the development of PCR diagnostic products and services in a collaborative lab environment.
- Company: Yourgene Health is a pioneering company in genomic medicine, focused on innovative diagnostic solutions.
- Benefits: Enjoy a competitive salary, benefits package, and a vibrant workplace culture.
- Why this job: Join a fast-paced team making impactful contributions to healthcare through cutting-edge technology.
- Qualifications: Requires a degree in life sciences and 7+ years of relevant industry experience.
- Other info: We value diversity and inclusion, ensuring everyone feels respected and empowered.
The predicted salary is between 36000 - 60000 £ per year.
Job title: Senior Scientist (PCR team)
Reports to: PCR Team Leader
Location: Manchester Science Park
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.
Yourgene primarily develops, manufactures, and commercialises simple and accurate molecular diagnostic solutions, for reproductive health, precision medicine and infectious diseases. The Group\’s flagship in vitro diagnostic products include non -invasive prenatal tests (NIPT) for Down\’s Syndrome and other genetic disorders, Cystic Fibrosis screening tests, invasive rapid aneuploidy tests and DPYD genotyping.
Yourgene has a range of innovative DNA sample preparation platforms, powered by Ranger® Technology, the Yourgene LightBench® and Yourgene QS250, ideal for cell free DNA applications in NIPT and oncology including liquid biopsy.
Yourgene also has a global laboratory service network equipped to be a full life-cycle partner for clinical, research and pharmaceutical organisations to support partners at the preclinical, clinical, and post market stage to develop, manufacture, obtain regulatory approval and commercialise new products and services. In addition, Yourgene offers and NIPT and high throughput Covid testing service.
Yourgene Health is headquartered in Manchester, UK with facilities in Taipei, Singapore, the US 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 nay social and well-being initiatives run by our Social Huddle that keep our sense of community alive during challenging times that the pandemic has thrown our way. 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:
Yourgene Health, part of the Novacyt Group, are recruiting for a Senior Scientist within our PCR Diagnostics Team based at Manchester Science Park. The Senior Scientist will work alongside the PCR Team Leader to lead the tactical delivery and development of PCR based in vitro diagnostic products and services.
Overall responsibility:
The Senior Scientist will provide scientific expertise and technical leadership on development projects ensuring tactical planning is performed effectively and consider problems at a system level. In addition, the Senior Scientist will design and develop in vitro PCR diagnostic products/ services for use in a range of applications to high quality and in a timely fashion. The scope will include PCR products developed in line with ISO 13485 and IVDR regulations.
Key areas of responsibility:
- Perform laboratory based technology development using molecular biology techniques including PCR and qPCR
- Independently design and execute experimental laboratory procedures
- Work collaboratively with others in the team, troubleshooting issues and suggesting next steps to resolve these whilst maintaining an innovative spirit
- Analyse experimental results, providing detailed conclusions and identifying technical solutions
- Effective management of required documentation in accordance with company Quality Management System and ISO 13485 regulations
- Provides scientific expertise and technical leadership on projects, as well as planning tactical delivery in functional area
- Lead and participate in activities requiring cross functional collaboration, including leading complex projects
- Support the resource planning activities of Team Leaders and Project Leaders
- Provide expertise into the creation, maintenance and improvement of;
- Overall process SOPs
- Process flows, standardized plans & reports
- Ensure planning and reporting of studies and work-packages is accurate and detailed
- Design effective and efficient studies involving;
- Accurate, efficient and timely documentation
- Developing and implementing protocols to show that tests meet acceptance criteria
- Data generation, ensuring integrity and organized data management
- Provide accurate, concise and independent data interpretation, factoring in systems-level thinking
- Determining test parameters, such as output specifications
- Meeting regulatory or other requirements
- Lead troubleshooting activities when technical issues arise
- Supports the development of external relationships, including through for example, grant applications, KOLs and partners
- Supports the identification of commercially and technically useful solutions for development
- Ensure own work meets regulatory & quality requirements (including compliance to SOPs, documentation using lab books, study plans, study reports and integrity of data)
- Ensure own work and that of junior staff is performed in line with company goals
- Provide support and guidance to junior staff
Qualifications, Skills and Abilities:
- Degree or further degree in a life science such as molecular biology, biochemistry or genetics
- Typically 7+ years of relevant industry experience
- Experience in the development, verification and validation of molecular diagnostics assays in adherence with CE marking and/or Design Control Regulations, ideally within IVDR and ISO 13485 regulations
- Hands on experience with PCR based assays including proficiency in primer and probe design and the use of Bioinformatics software (e.g. Geneious or equivalent)
- Analysis of data and interpretation of results
- Capable of independently performing experimental design and execution
- Enthusiasm, drive, thoroughness, diligence and a willingness to take personal responsibility to ensure that projects are successful
- Excellent communication, presentation and interpersonal skills
- Good organizational skills and thrives on working to tight deadlines
- Can summarize scientific data in written form to effectively communicate plans, progress and ideas with Management, Peers or External Audiences
- Good IT skills including Microsoft Office Suite and use of the statistical analysis software, JMP
Closing Date:
Sunday 19th January, 2025
Yourgene Health is committed to encouraging equality, diversity and inclusion among our workforce. The aim is for our workforce to be truly representative of all sections of society and for each employee to feel respected and able to give their best.
Yourgene Health | Senior Scientist (PCR team) employer: Yourgene Health
Contact Detail:
Yourgene Health Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Yourgene Health | Senior Scientist (PCR team)
✨Tip Number 1
Familiarize yourself with the latest advancements in PCR technology and molecular diagnostics. This will not only help you during the interview but also demonstrate your passion and commitment to the field.
✨Tip Number 2
Network with professionals in the genomics and diagnostics industry. Attend relevant conferences or webinars to connect with potential colleagues and learn more about Yourgene Health's work and culture.
✨Tip Number 3
Prepare to discuss specific projects you've worked on that align with the responsibilities of the Senior Scientist role. Highlight your experience with PCR assays, data analysis, and regulatory compliance to showcase your expertise.
✨Tip Number 4
Research Yourgene Health’s products and services thoroughly. Understanding their flagship products and recent innovations will allow you to engage in meaningful conversations during the interview process.
We think you need these skills to ace Yourgene Health | Senior Scientist (PCR team)
Some tips for your application 🫡
Understand the Role: Make sure to thoroughly read the job description for the Senior Scientist position. Highlight key responsibilities and qualifications that align with your experience, especially in PCR and molecular diagnostics.
Tailor Your CV: Customize your CV to reflect relevant experience in molecular biology, PCR techniques, and project management. Use specific examples from your past work that demonstrate your expertise and achievements in these areas.
Craft a Compelling Cover Letter: Write a cover letter that not only outlines your qualifications but also expresses your enthusiasm for working at Yourgene Health. Mention how your values align with their culture of innovation and collaboration.
Highlight Team Collaboration: In your application, emphasize your ability to work collaboratively within a team. Provide examples of past projects where you successfully led or contributed to cross-functional teams, showcasing your leadership and communication skills.
How to prepare for a job interview at Yourgene Health
✨Showcase Your Technical Expertise
Be prepared to discuss your hands-on experience with PCR and qPCR techniques. Highlight specific projects where you designed and executed experimental procedures, and be ready to explain the outcomes and any challenges you faced.
✨Demonstrate Problem-Solving Skills
Yourgene values innovative thinking. Prepare examples of how you've approached troubleshooting in past projects. Discuss how you identified issues, proposed solutions, and implemented changes effectively.
✨Emphasize Collaboration
Since the role involves cross-functional collaboration, share experiences where you worked as part of a team. Highlight your ability to communicate effectively and lead projects while supporting junior staff.
✨Understand Regulatory Standards
Familiarize yourself with ISO 13485 and IVDR regulations. Be ready to discuss how you have ensured compliance in previous roles, particularly in the development and validation of molecular diagnostics assays.
