Careers in Personalised Medicine for Cancer Patients

MDxHealth seeks talented people who are passionate about improving the diagnosis and treatment of cancer patients.

MDxHealth offers a rewarding work environment with career opportunities in the growing cancer genomics arena. We seek experienced, highly motivated professionals who are dedicated to working side by side to achieve the company’s goal of improving patient care.

MDxHealth is building a world class healthcare company, providing significant career development and financial opportunities. If you have interest in joining the MDxHealth team, please contact our Human Resources Department.

Product Development Scientist/Senior Product Development Scientist

Job Description:

The Product Development Scientist will support the development of molecular diagnostic oncology tests to be offered in our CLIA laboratory. In this hands-on position, the Scientist will be responsible for: 1)  Development of molecular diagnostic qPCR assays. 2) Ensuring the successful transfer and validation of the tests in the CLIA lab. 3) The successful candidate must be able to work effectively across functional disciplines, under tight deadlines with minimal supervision.

• Design and develop molecular diagnostic assays under Design Controls from late stage feasibility through test launch. Identify all issues critical to successful test development and manufacture
• Evaluate suppliers of equipment, materials and reagents for suitability in product
  development and assay component manufacturing
• Apply knowledge of molecular biology and oncology to evaluate and create new methods and procedures as needed
• Perform lab work according to internal quality standards, document accurately the results and archive them accordingly in order to facilitate downstream work (intellectual property, regulatory affairs or research follow-ups)
• Analyse results using statistical methods, control for consistency with previous work, summarise and communicate main outcomes to team members
• Prepare experimental plans and protocols, technical reports, summaries, and quantitative analyses that accurately and clearly communicate necessary information.
• Drive creation of all necessary documentation to support test manufacture, including manufacturing specifications, QC test procedures, raw material specifications and validation protocols.
• Effectively drive transfer and validation of new tests into the clinical laboratory
• Utilize independent project management and cross-functional teamwork skills to ensure
  timely and reliable results

Desired Skills & Experience

• Advanced degree (Ph.D. or M.S.) in molecular biology or related discipline
• A strong foundational knowledge of molecular biology
• At least 5 years' experience in advanced molecular assay development, especially qPCR
• IVD Industry experience with proven history of delivering commercially successful results
  and working under Design Controls.
• Strong problem solving and bench scientist skills and ability to work independently
• Strong written and verbal communication skills required