Responsibilities
- 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
Requirements
- 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
- Good organization skills, detailed oriented mindset
- Ability to thrive in a fast paced environment
Hard Skills
- Assay Characteristics Knowledge
- R&D Design Document Management
- Laboratory Validation
- Workflow And SOP Development
- Assay Performance Specifications Design
- Technical Issue Troubleshooting
- Project Budget Tracking
Soft Skills
- Leadership Capabilities
- Good Organization Skills
- Detail Oriented Mindset
- Ability To Thrive In Fast Paced Environment
Senior Scientist – R&D in chicago at Unknown Company
This position is listed as full time and onsite.