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Research And Development Scientist

Job in Bartlett, Shelby County, Tennessee, USA
Listing for: Ospri BioPath
Full Time position
Listed on 2026-08-18
Job specializations:
  • Quality Assurance - QA/QC
    Regulatory Compliance Specialist
  • Research/Development
    Regulatory Compliance Specialist, Medical Science
Salary/Wage Range or Industry Benchmark: 70000 - 100000 USD Yearly USD 70000.00 100000.00 YEAR
Job Description & How to Apply Below

We are seeking a detail-oriented Validation Scientist to design, execute, and document validation and verification studies for laboratory assays and instrumentation. The successful candidate will ensure that test methods perform reliably, meet regulatory and quality requirements, and are ready for routine use. Experience with molecular assays (e.g., PCR, qPCR, dPCR) is strongly preferred, though candidates with strong general assay validation experience are encouraged to apply.

Key Responsibilities
  • Plan, execute, and document method validation and verification studies in accordance with applicable regulatory and quality standards.
  • Author and review validation protocols, test plans, reports, and standard operating procedures (SOPs).
  • Analyze validation data, interpret results, and present clear conclusions with supporting statistics.
  • Troubleshoot assay and instrument performance issues and recommend corrective actions.
  • Support technology transfer of new or modified assays from development into routine use.
  • Maintain accurate, audit-ready documentation and records.
  • Collaborate with R&D, quality control, and production teams to meet project timelines.
Required Qualifications
  • Bachelor's or Master's degree in a life science discipline (Molecular Biology, Biochemistry, Microbiology, Biotechnology, Chemistry, or a related field).
  • Hands-on experience with validation and verification testing of laboratory assays or instruments.
  • Working knowledge of assay performance parameters and the statistics used to evaluate them.
  • Strong technical writing skills for protocols, reports, and SOPs.
  • Solid attention to detail, documentation discipline, and organizational skills.
  • Ability to work independently and as part of a cross-functional team.
Preferred Qualifications
  • Experience validating molecular assays (PCR, real-time/qPCR, next-generation sequencing, or similar).
  • Familiarity with regulated laboratory environments (CLIA, ISO 13485, GLP/GMP, or FDA/IVD).
  • Experience with data analysis and statistical tools.
  • Understanding of quality management systems, deviations, and change control.
  • Analytical and problem-solving mindset.
  • Clear written and verbal communication.
  • Ability to manage multiple projects and meet deadlines.
  • Commitment to quality, accuracy, and continuous improvement.
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