At Alamar, we are passionate about enabling our customers to make scientific discoveries that translate into clinical outcomes and benefit patients. Our team is growing quickly as we develop innovative approaches to measure critical protein biomarkers from liquid samples that can enable the earliest possible detection of disease. We believe the next frontier in biology is enabled by measuring proteins at higher sensitivity in highly multiplexed assays at the push of a button, which is something only Alamar can do. As we build our team, we seek collaborative, driven, intellectually curious people committed to solving complex challenges. Our culture rewards accountability and cross functional teamwork because we believe this enables the kind of breakthrough thinking that will accelerate our mission.
Position Summary
We are seeking a highly motivated Sr. Scientist I to join the Product Development team supporting New Product Introduction (NPI). This role focuses on downstream product development, including QC method development, analytical strategy, process optimization, and transfer of assays and reagents from R&D into Manufacturing. The Product Development team operates at the interface of R&D and Operations and is responsible for ensuring products are robust, scalable, and manufacturable.
Duties and Responsibilities
- Design, develop, and optimize QC methods to characterize assay performance, reagent quality, and product consistency
- Define QC strategies across the product lifecycle, including raw material, in-process, and finished goods QC
- Design and execute V&V studies including precision, sensitivity, linearity, and robustness testing
- Support end-to-end product development from late-stage R&D through commercialization
- Lead or support product and process transfer to Manufacturing, including documentation and training
- Develop scalable and robust production processes for complex assay and reagent systems
- Troubleshoot process and QC issues during transfer and early manufacturing runs
- Collaborate with R&D, Manufacturing, QC, Quality, and Engineering teams
- Author SOPs, validation reports, and transfer documentation
- Lead or support root cause investigations and continuous improvement initiatives
Qualifications
- Ph.D. in Biochemistry, Molecular Biology, Immunology, or a related discipline with 5+ years OR M.S. with 8+ years of relevant industry experience
- Deep expertise in QC method development, validation, and transfer to manufacturing
- Experience leading NPI and product transfer efforts for commercially successful biotech tools or diagnostic products
- Strong background in assay development, reagent formulation, and analytical methods
- Experience with writing technical documentation including SOPs and validation reports
- Strong problem solving and troubleshooting skills
- Experience with immunoassays (ELISA, MSD, Simoa) and molecular assays (qPCR, ddPCR, NGS)
- Experience working in IVD or regulated environments (e.g., ISO 13485)
- Familiarity with statistical analysis tools such as JMP
- Understanding of manufacturing and scale-up considerations
- Demonstrated ability to work effectively as a team player, collaborating openly and constructively within cross-functional teams
The base salary range for this full-time position is $150,000 - $165,000 + bonus + equity + benefits. Our salary ranges are determined by work location, job-related skills, experience, and relevant education or training. The ranges displayed on each job posting reflect the minimum and maximum target for new hire salaries but are subject to change if the leveling of the role is adjusted. Your recruiter can share more about the specific salary range during the hiring process.
Please Note - We participate in E-Verify to confirm authorization to work in the United States.
Skills Required
- Ph.D. in Biochemistry, Molecular Biology, Immunology, or related discipline with 5+ years OR M.S. with 8+ years of relevant industry experience
- Deep expertise in QC method development, validation, and transfer to manufacturing
- Experience leading NPI and product transfer efforts for commercially successful biotech tools or diagnostic products
- Strong background in assay development, reagent formulation, and analytical methods
- Experience writing technical documentation including SOPs and validation reports
- Strong problem solving and troubleshooting skills
- Experience with immunoassays (ELISA, MSD, Simoa) and molecular assays (qPCR, ddPCR, NGS)
- Experience working in IVD or regulated environments (e.g., ISO 13485)
- Familiarity with statistical analysis tools such as JMP
- Understanding of manufacturing and scale-up considerations
- Demonstrated ability to work effectively as a team player in cross-functional teams
What We Do
Alamar Biosciences is powering precision proteomics with automated, high throughput solutions for ultra-high sensitivity protein analysis across a range of multiplex levels. Our proprietary NULISA™ Chemistry utilizes a novel sequential capture and release method that significantly reduces background signal and increases the sensitivity and dynamic range compared with standard approaches and allows both qPCR and NGS readouts. The NULISAseq Inflammation Panel contains 200+ important markers related to immune and inflammatory diseases and will run on our ARGO™ System. This innovative platform allows for a fully automated workflow with less than 30 minutes hands on time from sample to data
