Research and Development Scientist

Multiplex PCR Research Scientist – BioGX

Perform laboratory research to develop multiplex PCR tests for a variety of real‑time PCR platforms. This involves using both automated and non‑automated PCR instruments, planning experiments, evaluating and selecting target sequences through scientific literature research, analyzing data, documenting, summarizing research, and transferring developed tests. All protocols, reports, and other documented information meet QMS requirements.

• Use chemistry, biochemistry, and molecular biology knowledge to solve development problems associated with genetic tests for specific DNA and RNA sequences.
• Supervise R&D associates, work in the laboratory, and participate on product transfer teams.
• Carry out design‑of‑experiments (DOE) studies needed to establish robust PCR‑based genetic test performance and use experimental results to develop raw material requirements, product performance specifications, packaging requirements, stability characteristics, and manufacturing release test criteria.
• Perform feasibility and development experiments, develop protocols and procedures using Good Documentation Practices and provide clear, professional report writing to support timely project completion.
• Maintain current knowledge of competitive technologies, new principles, and theories relevant to product R&D and commercialization.
• Train, motivate, and develop R&D staff as needed.
• Document experimental protocols, study results, and process design/development history to meet QMS requirements.

• Experience with nucleic acid, PCR‑based diagnostic test product development.
• Experience with DNA and RNA sample processing and sample stabilization procedures.
• Experience with BSL‑2 procedures and safe handling of human blood and fluids for purified nucleic acid acquisition.
• Direct experience with ISO design control procedures and participation in development, verification, validation stages for technology transfer into a GMP manufacturing unit.
• Well organized and efficient at handling multiple tasks simultaneously.
• Technician supervisory experience.
• Experience with short, intermediate, and long‑term project planning and clinical research.
• Fluent in Microsoft Word, Excel, and PowerPoint.
• Excellent written and verbal communication skills.
• Work seamlessly in a team environment, relating effectively to both highly educated and unskilled team members.
• Ability to resolve conflicts and perform well under stressful conditions.
• Ph.D. or M.S. (plus 2–5 years experience) in Microbiology, Molecular Biology, or a related field. Direct experience with Real‑Time qPCR is desirable.

Mid‑Senior level

Full‑time

Research, Analyst, and Information Technology