Alamar Biosciences, Inc.
Overview
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Analyst II, Quality Control
role at
Alamar Biosciences, Inc.
We are on a mission to transform proteomics for early detection of cancer and other diseases, and we are building a high-throughput, automated platform to support biomarker discovery and disease prevention. We provide opportunities for entrepreneurial individuals who enjoy developing novel technologies and growing with the company. Position Description
We seek a highly motivated Quality Control Analyst II to join our Operations team. This position will be part of the Quality Control team, supporting all product testing activities from raw materials to finished goods, as well as product stability. The role will also involve data evaluation, troubleshooting, and helping streamline processes, while adhering to ISO 13485/GMP requirements. Key Responsibilities
Perform analytical/functional testing for in-process and finished goods on manufactured products. Perform analytical/functional testing on incoming raw materials. Perform product testing to support product stability/dating. Review data and assess against established acceptance criteria. Prepare QC reference test materials per established procedures. Record, track, and maintain QC data in logs and spreadsheets for trending. Revise and update QC testing procedures and documentation for better workflow. Generate data and graphs for trending test results. Initiate and participate in nonconformance/deviation and troubleshooting activities. Generate equipment operation and maintenance SOPs. Participate and provide support in streamlining QC workflow. Occasional Duties and Responsibilities
Perform testing on non-routine samples to establish QC specifications. May assist in performing incoming inspection and visual inspection of manufactured products. Participate in Test Method Validation. Qualifications
B.S./B.A. in molecular biology, biochemistry, cell biology or related field with 2-3 years of industry laboratory experience, preferably in a Quality Control laboratory. Experience in molecular biology techniques. Detail-oriented, organized, and efficient. Strong team player who can also work independently. Excellent verbal and written communication skills. Experience working in ISO 13485 and GMP environment, preferably in QC processes. The base salary range for this full-time position is $80,000 - $95,000 plus bonus, equity, and benefits. Salary ranges are determined by location, skills, experience, and education. Ranges reflect minimum and maximum targets for new hires and may change if leveling is adjusted.
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Join to apply for the
Analyst II, Quality Control
role at
Alamar Biosciences, Inc.
We are on a mission to transform proteomics for early detection of cancer and other diseases, and we are building a high-throughput, automated platform to support biomarker discovery and disease prevention. We provide opportunities for entrepreneurial individuals who enjoy developing novel technologies and growing with the company. Position Description
We seek a highly motivated Quality Control Analyst II to join our Operations team. This position will be part of the Quality Control team, supporting all product testing activities from raw materials to finished goods, as well as product stability. The role will also involve data evaluation, troubleshooting, and helping streamline processes, while adhering to ISO 13485/GMP requirements. Key Responsibilities
Perform analytical/functional testing for in-process and finished goods on manufactured products. Perform analytical/functional testing on incoming raw materials. Perform product testing to support product stability/dating. Review data and assess against established acceptance criteria. Prepare QC reference test materials per established procedures. Record, track, and maintain QC data in logs and spreadsheets for trending. Revise and update QC testing procedures and documentation for better workflow. Generate data and graphs for trending test results. Initiate and participate in nonconformance/deviation and troubleshooting activities. Generate equipment operation and maintenance SOPs. Participate and provide support in streamlining QC workflow. Occasional Duties and Responsibilities
Perform testing on non-routine samples to establish QC specifications. May assist in performing incoming inspection and visual inspection of manufactured products. Participate in Test Method Validation. Qualifications
B.S./B.A. in molecular biology, biochemistry, cell biology or related field with 2-3 years of industry laboratory experience, preferably in a Quality Control laboratory. Experience in molecular biology techniques. Detail-oriented, organized, and efficient. Strong team player who can also work independently. Excellent verbal and written communication skills. Experience working in ISO 13485 and GMP environment, preferably in QC processes. The base salary range for this full-time position is $80,000 - $95,000 plus bonus, equity, and benefits. Salary ranges are determined by location, skills, experience, and education. Ranges reflect minimum and maximum targets for new hires and may change if leveling is adjusted.
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