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- Tasks: Conduct research and product development in medical devices with minimal supervision.
- Company: Join a leading company in the medical device sector, focused on innovation and quality.
- Benefits: Enjoy flexible hours, travel expenses covered, and potential for permanent employment.
- Why this job: Make a real impact in healthcare while working in a supportive and dynamic environment.
- Qualifications: PhD or MSc in microbiology; experience in regulated industries preferred.
- Other info: Role based in Liverpool, moving to a modern site in Deeside.
The predicted salary is between 36000 - 60000 £ per year.
Type: 12 month FTC (has the potential to go permanent /to be reviewed at the end of the term)
Location: Liverpool initial (role will be moving to Deeside long term at their new modern site)
Hours: 8:30 - 16.30 Mon-Fri with some flex if needed (onsite)
NB expenses will be provided when travelling to Liverpool *tunnel etc.
The Role:
- To be responsible for carrying out existing and new product development activities as agreed under the general supervision of the line manager. All activities are to be conducted to the agreed scientific and regulatory standard or directives e.g. European IVDD and IVDR of the department and promptly reporting deviations from stated targets of performance.
- To be responsible, with minimum supervision, for conducting reviews of literature related to investigations being undertaken, conducting and, where necessary, enhancing experimental design, carrying out research studies, analysis of experimental data, reporting of studies in the form of a written report as per laboratory standards and ensuring raw materials are available as required for investigative studies.
- To be responsible for performing scientific and documentary activities related to regulatory requirements e.g. European IVDD and IVDR, to the agreed scientific and regulatory standards and promptly reporting deviations.
- To ensure products are designed and manufactured with sufficient robustness, so they do not compromise the health and safety of patients, users and third parties and attain the performance levels specified by the manufacturer.
- Supporting senior staff to provide a high standard of technical service and support including the investigation of customer complaints, production problems and assistance with validation studies.
- To be responsible for the collation of reference information relevant to all investigations and for the correct maintenance and updating of technical records in appropriate project files for allocated projects.
- To participate in laboratory project meetings where technical matters affecting current projects and present results are discussed.
- To provide assistance to senior staff in technical training for Sales and Marketing and laboratory personnel.
- To provide cover for Quality Control staff, as agreed between the Quality Control and R&D Managers when necessary.
- Prepare and present written reports and documents as directed, including the preparation and updating of Standard Operating Procedures, technical dossiers demonstrating product compliance with regulatory standards or directives, reports and documents for company policy and other meetings.
- To use specialised technical knowledge and skills to work on the development, documentation and evaluation of new products.
- To perform investigations related to the improvement of existing products and to investigate resolution of manufacturing issues.
- To apply a good understanding of QA, GMP, IVD Directive (IVDD) and Regulation (IVDR), ISO 9001 and ISO 13485 guidelines to Client Group products, allowing them to meet regulatory and market requirements and to generate significant profit for the company over their lifecycle.
The Person:
- Will hold a degree in a relevant microbiology-based subject (the ideal Candidate will hold an MSc but not essential).
- The ideal Candidate will have experience working in an ISO 13485, IVDR (or related) - regulated industry.
- Experience in bacteriology with an emphasis on conventional techniques over molecular techniques.
- Proven report writing skills.
Important Information: We endeavour to process your personal data in a fair and transparent manner. In applying for this role, Russell Taylor will be acting within your interest and will contact you in relation to the role, either by email, phone or text message. For more information see our Privacy Policy on our website. It is important you are aware of your individual rights and the provisions the company has put in place to protect your data. If you would like further information on the policy or GDPR please get in touch with us here.
Research Scientist, Medical Devices, PhD employer: Russell Taylor Group Ltd
Contact Detail:
Russell Taylor Group Ltd Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Research Scientist, Medical Devices, PhD
✨Tip Number 1
Familiarise yourself with the European IVDD and IVDR regulations, as well as ISO 13485 standards. Understanding these guidelines will not only help you in interviews but also demonstrate your commitment to compliance and quality in medical device development.
✨Tip Number 2
Network with professionals in the medical devices field, especially those who have experience in IVD. Attend relevant conferences or webinars to connect with potential colleagues and learn about the latest trends and challenges in the industry.
✨Tip Number 3
Prepare to discuss specific examples of your previous research projects, particularly those involving bacteriology and conventional techniques. Being able to articulate your hands-on experience will set you apart from other candidates.
✨Tip Number 4
Showcase your report writing skills by preparing a mock report based on a hypothetical research study. This will not only help you practice but also give you a tangible example to discuss during your interview, highlighting your ability to communicate complex information effectively.
We think you need these skills to ace Research Scientist, Medical Devices, PhD
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in microbiology and any work you've done in ISO 13485 or IVDR regulated environments. Emphasise your report writing skills and any specific projects that align with the job description.
Craft a Strong Cover Letter: In your cover letter, explain why you're interested in the Research Scientist position and how your background makes you a suitable candidate. Mention your familiarity with regulatory standards like IVDD and IVDR, and provide examples of your previous work that demonstrate your capabilities.
Highlight Relevant Skills: Clearly outline your skills related to experimental design, data analysis, and technical documentation. Make sure to mention any experience you have with customer complaints or production problems, as these are key aspects of the role.
Proofread Your Application: Before submitting, carefully proofread your application for any spelling or grammatical errors. A well-presented application reflects your attention to detail, which is crucial in a scientific role.
How to prepare for a job interview at Russell Taylor Group Ltd
✨Know Your Regulations
Familiarise yourself with the European IVDD and IVDR regulations. Being able to discuss how your experience aligns with these standards will show that you understand the regulatory landscape and can contribute effectively to the role.
✨Demonstrate Your Research Skills
Prepare to discuss specific research projects you've worked on, particularly those involving bacteriology and conventional techniques. Highlight your ability to design experiments, analyse data, and report findings clearly.
✨Showcase Your Report Writing Abilities
Since proven report writing skills are essential for this role, be ready to provide examples of reports you've written in the past. Discuss the structure, clarity, and detail you included to meet laboratory standards.
✨Engage in Technical Discussions
Be prepared to participate in discussions about technical matters relevant to the role. This could include sharing insights from literature reviews or discussing how you would approach resolving manufacturing issues.
