Senior QC Scientist I

Alamarbiosciences; Fremont (CA); On-site; USD 150,000 - 165,000; Full time

Benefits offered by this job

Bonus

Equity

Benefits

Job summary

Alamarbiosciences seeks a highly skilled Sr. QC Scientist I for the Operations team, starting with a 6-month onboarding in Product Development. After training on the NULISAseq platform, you will lead QC, troubleshooting, and batch release for antibody pools, ensuring high quality and compliance.

Role blends scientific rigor with manufacturing discipline, offering opportunities to drive continuous improvement in QC strategies and data-driven investigations across production and quality teams.

Qualifications

• PhD (Biochemistry, Molecular Biology, Immunology) with 5+ years of industry experience or MS with 8+ years of relevant industry experience.
• Background in NGS and immunoassays; experience with single-molecule or multiplexed protein detection platforms is a plus.
• Ability to analyze large complex datasets and identify meaningful issues efficiently.
• Strong QC principles knowledge, data-driven root cause analysis, and traceability practices.
• Experience writing and executing SOPs and batch records in a regulated environment (ISO 13485 or equivalent).
• Excellent organizational skills and ability to maintain full traceability across materials and processes.

Responsibilities

• Develop understanding of the NULISAseq antibody pool formulation process and data interpretation.
• Coordinate production and accurate pooling of antibodies per protocols.
• Perform in-process and finished goods QC on NULISAseq products.
• Analyze multi-analyte NGS datasets to evaluate performance metrics and root causes.
• Troubleshoot QC failures with data-driven investigations to meet production and quality needs.
• Maintain records to support traceability and root cause analysis.
• Author and review SOPs, batch records, and COAs under ISO/GMP standards.
• Collaborate with Tech Transfer on QC strategy, method qualification/validation, and transfer.

Skills

NGS data analysis

Immunoassays QC

SOP writing and documentation

Troubleshooting

Cross-functional communication

Attention to detail

Data interpretation

Education

PhD in Biochemistry / Molecular Biology / Immunology

MS in Biochemistry / Molecular Biology / Immunology

Tools

Hamilton liquid handling

Python / R / JMP

Job description

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.

We are seeking a highly skilled and quality-driven Sr. QC Scientist I to join our Operations team in a role that begins with an intensive 6-month onboarding period embedded within our Product Development group. During this period, the Sr. QC Scientist will receive comprehensive training in Alamar’s NULISAseq platform, antibody pool production processes, and our suite of QC methodologies. Upon completing this training, the Sr. QC Scientist will transition to Operations, where they will be the primary owner of building, QC, and troubleshooting for Alamar’s NULISAseq antibody pools. This role sits at the intersection of scientific rigor and manufacturing discipline and is critical to ensure that every panel we release meets the highest standards of quality and performance.

Responsibilities

• Develop deep understanding of the NULISAseq antibody pool formulation process and interpretation of the data generated.
• Coordinate the production of NULISAseq antibody pools, including accurate pooling of all antibodies, using established protocols.
• Perform in-process QC and finished goods QC on NULISAseq products.
• Analyze complex, multi-analyte NGS datasets to evaluate product performance metrics; identify meaningful deviations and drive targeted investigations to root cause.
• Troubleshoot pool QC failures using structured, data-driven root cause investigations in a timely manner to meet both production needs and quality standards.
• Track and maintain records to support traceability and root cause analysis.
• Author, review, and execute SOPs and batch records in compliance with ISO 13485 and/or GMP quality standards.
• Collaborate with Tech Transfer Team on the establishment of QC strategies, including method qualification/validation, specifications setting, and method transfer for new and existing products. Support the generation of Certificates of Analysis (COAs) and release documentation for manufactured antibody pools.
• Collaborate closely with Product Development, Quality, and Manufacturing teams to communicate QC outcomes, elevate failures, and drive continuous improvement.
• Maintain an organized, controlled, and inspection-ready work area; enforce safe work practices and compliance expectations.
• Contribute to the development and refinement of QC acceptance criteria and troubleshooting decision frameworks as new panels and lots are introduced.

Qualifications

• D. in Biochemistry, Molecular Biology, Immunology, or a related discipline with 5+ years, OR M.S. with 8+ years of relevant industry experience.
• Background in next-generation sequencing (NGS) and immunoassays; experience with proximity ligation, proximity extension, or related single-molecule or multiplexed protein detection platforms is a plus.
• Demonstrated ability to analyze and interpret large, complex datasets, with proficiency to efficiently identify meaningful issues in the data.
• Strong working knowledge of immunoassay QC principles, including signal characterization and failure mode analysis.
• Exquisite attention to detail and an uncompromising commitment to quality - this role requires precision at every step, from in-lab execution to documentation to data review.
• Experience writing and executing SOPs, batch records, and other controlled documents in a regulated environment (ISO 13485 or equivalent).
• Excellent organizational and record-keeping skills; ability to maintain full traceability across raw materials, in-process steps, and finished goods.
• Strong troubleshooting skills; able to work through complex, multi-variable failure modes systematically and with scientific rigor.
• Effective communicator who can clearly convey QC findings and escalation needs to cross-functional partners.

Preferred Qualifications

• Experience with antibody-oligonucleotide conjugation chemistry and quality assessment of conjugated products.
• Familiarity with high-plex proximity-based immunoassays or other highly complex products.
• Experience with automated liquid handling platforms, particularly Hamilton, and automated assay systems.
• Proficiency in data analysis tools such as R, Python, or JMP for processing NGS-based QC data.
• Experience supporting or leading root cause investigations and CAPA processes in a quality system context.

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.

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