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Principal Scientist Assay Development Jobs in Georgia

Senior Scientist, Molecular Assay Development in R&D Passionate about precision medicine and advancing the healthcare industry? Recent advancements in underlying technology have finally made it ...

Lead development, optimization, and commercialization of new products serving the rubber and tire industry. * Identify and champion technology opportunities that strengthen existing product lines and ...

Principal Scientist

Macon, GA · On-site

$140 - $210/hr

Principal Scientist - Rubber & Tire Technologies Location: Macon, GA Department: Research ... Lead development, optimization, and commercialization of new products serving the rubber and tire ...

Lead development, optimization, and commercialization of new products serving the rubber and tire industry. * Identify and champion technology opportunities that strengthen existing product lines and ...

Lead development, optimization, and commercialization of new products serving the rubber and tire industry. * Identify and champion technology opportunities that strengthen existing product lines and ...

We are seeking a Principal Data Scientist in Atlanta to design, build, and validate agentic AI ... Scaling AI initiatives and agentic development across Invesco Technology teams by creating reusable ...

We are seeking a Principal Data Scientist in Atlanta to design, build, and validate agentic AI ... Scaling AI initiatives and agentic development across Invesco Technology teams by creating reusable ...

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Principal Scientist Assay Development information

What does a principal scientist assay development do?

A Principal Scientist in Assay Development leads the design, optimization, and validation of assays used for research, diagnostics, or drug development. They oversee laboratory teams, develop protocols, and ensure that assays meet regulatory and quality standards. Their role also involves troubleshooting complex scientific problems, collaborating with cross-functional teams, and staying current with technological advances in assay technologies. Principal Scientists play a key role in translating scientific concepts into reliable, reproducible assays that support broader organizational goals.

What are some common challenges faced by principal scientists assay development, and how can they be addressed?

Principal Scientists in Assay Development often encounter challenges such as optimizing assay sensitivity and specificity, troubleshooting inconsistent results, and scaling up assays for high-throughput screening. Addressing these issues requires strong analytical thinking, effective cross-functional collaboration with research, engineering, and quality assurance teams, and staying updated with the latest technological advances. Regularly reviewing validation protocols and actively participating in peer discussions can also help in overcoming technical hurdles and ensuring robust assay performance.

What are the key skills and qualifications needed to thrive as a principal scientist assay development, and why are they important?

To thrive as a Principal Scientist Assay Development, you need advanced expertise in biochemistry or molecular biology, a PhD or equivalent experience, and a strong background in assay design and validation. Familiarity with laboratory automation, data analysis software, and regulatory compliance systems such as GLP/GMP is typically required. Leadership, project management, and effective communication are crucial soft skills for guiding teams and collaborating across departments. These skills ensure robust assay performance, regulatory adherence, and efficient innovation in complex scientific environments.

What is the difference between Principal Scientist Assay Development vs Senior Scientist Assay Development?

AspectPrincipal Scientist Assay DevelopmentSenior Scientist Assay Development
CredentialsAdvanced degree (PhD or equivalent), extensive experienceMaster's or PhD, significant industry experience
Work EnvironmentLeads assay development projects, strategic planningExecutes assay development tasks, supports project teams
Employer & Industry UsagePharmaceutical, biotech, CROs, biotech companiesPharmaceutical, biotech, research labs

The main difference between Principal Scientist Assay Development and Senior Scientist Assay Development lies in their level of responsibility and leadership. Principal Scientists typically lead projects, set strategies, and have more extensive experience, while Senior Scientists focus on executing assays and supporting project goals. Both roles require strong technical expertise, but the Principal Scientist position involves higher-level decision-making and oversight.

What job categories do people searching Principal Scientist Assay Development jobs in Georgia look for?

The top searched job categories for Principal Scientist Assay Development jobs in Georgia are:

What cities in Georgia are hiring for Principal Scientist Assay Development jobs?

Cities in Georgia with the most Principal Scientist Assay Development job openings:

Infographic showing various Principal Scientist Assay Development job openings in Georgia as of August 2026, with employment types broken down into 74% Full Time, 13% Part Time, and 13% Contract. Highlights an 100% In-person job distribution.

$94K - $135K/yr

Full-time

Re-posted 25 days ago


Job description

Passionate about precision medicine and advancing the healthcare industry?

Recent advancements in underlying technology have finally made it possible for AI to impact clinical care in a meaningful way. Tempus' proprietary platform connects an entire ecosystem of real-world evidence to deliver real-time, actionable insights to physicians, providing critical information about the right treatments for the right patients, at the right time.

Senior Scientist, Molecular Assay Development in R&D

Passionate about precision medicine and advancing the healthcare industry?

Recent advancements in underlying technology have finally made it possible for AI to impact clinical care in a meaningful way. Tempus' proprietary platform connects an entire ecosystem of real-world evidence to deliver real-time, actionable insights to physicians, providing critical information about the right treatments for the right patients, at the right time.

We are looking for a Senior Scientist within the Molecular Assay Development group to co-lead the design and development of assays in support of IVD & CDx programs. In this role you will lead projects with staff scientists that lead the wet lab efforts during development and guide documentation specialists to assist in IVD documentation efforts. You will rise to the challenge of designing, supporting and documenting V&V studies for molecular assays, ensure project deliverables are compliant with applicable regulations, and provide technical reports to support FDA submissions. You are expected to collaborate cross-functionally with members of technology development, bioinformatics, quality control, regulatory affairs, and the clinical lab.

What you'll do:

  • Maintain overall knowledge of the assay characteristics

  • Provide scientific leadership to cross-functional teams

  • Manage and lead generation of R&D design documents

  • Lead validation team from project inception through launch including sample selection, hands-on laboratory validation, establishing workflow and SOPs, and authoring validation plans and summaries

  • Ensure activities are consistent with project critical path and respond appropriately to changing priorities

  • Assist in developing and tracking project budgets

  • Design assay performance specifications

  • Ensure assay development process meets milestones and timelines

  • Troubleshoot and solve technical issues

  • Maintain compliant laboratory documents and procedures

  • Proactively improve efficiency, quality and effectiveness of R&D efforts

Qualifications:

  • PhD in Nucleic Acids Biochemistry, Molecular Biology, or related field with 3+ years industry experience -or- MS with industry experience commensurate with requirements

  • Demonstrated leadership capabilities in assay development in an FDA regulated environment for IVD products under design controls

  • Strong technical expertise and hands on experience with nucleic acid technologies with a preference towards NGS, PCR, and qPCR techniques

  • Proven ability to apply principles of quality control and quality assurance to development activities

  • Strong understanding of FDA, EUA, and other global regulatory requirements

  • Demonstrated technical and project leadership expertise

  • Good organization skills, detailed oriented mindset

  • Ability to thrive in a fast paced environment

  • Team driven


$94,000.00-$135,000.00

The expected salary range above is applicable if the role is performed from Illinois and may vary for other locations (California, Colorado, New York). Actual salary may vary based on qualifications and experience. Tempus offers a full range of benefits, which may include incentive compensation, restricted stock units, medical and other benefits depending on the position.

We are an equal opportunity employer. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.