Standard BioTools
Overview
Join to apply for the QC Analyst I role at Standard BioTools. Would you like to join an innovative team driven by a bold vision – unleashing tools to accelerate breakthroughs in human health? We invite you to join a leading provider of indispensable life sciences tools that is accelerating global research on multiple frontiers of human health. At Standard BioTools, we are building a positive culture where our people can do the best work of their careers, informed and influenced by our core behaviors: Keep customers front and center in all of our work Be accountable and deliver on commitments Drive continuous improvement Be collaborative and work as one team: fostering communications in a learning, coaching, and helpful environment We are currently looking for a QC Analyst to perform analytical testing of raw materials, finished product, stability samples, and R&D materials as part of the quality team. Key Job Responsibilities
Complying with cGMPs, CLIA regulations, SOPs, safety requirements, and all company policies and procedures Take ownership of and responsibility for analytical testing, including supporting method development or optimization as needed Generating and maintaining laboratory data and records in accordance with company policies Conducting product stability testing in accordance with defined schedule (per protocol) Functional analysis of material to determine binding efficiency, specificity, and other parameters as required. Testing may be performed in support of multiple working groups Analytical analysis of material to determine identity, purity, conformance to release specifications and other testing parameters Independently perform and adequately document basic investigations for out-of-specification or out-of-trend results Assisting or leading the execution / implementation of larger projects, including revising/improving test methods, SOP revisions, process improvement projects, etc. As appropriate, will cross-train in other departments or job functions to meet production or assay timelines when needed Participates in departmental or cross functional projects Qualifications
Education
Bachelor’s Degree – major in biology, chemistry, or related science is required Skills And Experience
0 - 5 years of experience in a Quality Control work environment, preferably in the pharmaceutical or medical device industries, working under cGMP or ISO regulations Ability to test raw materials, in-process materials, and finished products Experience with ELISA, microbiology, PCR, or related test methods Experience with HPLC, MS, UV-Vis, and related test methods Devise solutions for complex problems Ability to prioritize and meet deadlines, ability to multi-task effectively Learn to utilize new software as it relates to job function Strong communication and presentation skills, including technical writing and reporting Ability to build and maintain effective relationships across departments and working groups Proficient in MS Office applications, highly proficient in Excel Work Environment
Ability to work in a fast-paced environment As Somalogic is a Hazardous Waste Generator, this position performs hazardous waste duties in accordance with internal controlled documents, local, State and Federal regulations Works in a laboratory setting. The individual will be required to enter production support areas and laboratories while wearing appropriate PPE (personal protective equipment) such as lab coat, gloves and safety glasses. Note: Potential to work in proximity to patient samples, including blood, plasma, CSF, and other matrices, including known and suspected infectious material. Salary Range
$54,200 - $63,000 Annual Equal Employment Opportunity Statement
All qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status or other legally protected status.
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Join to apply for the QC Analyst I role at Standard BioTools. Would you like to join an innovative team driven by a bold vision – unleashing tools to accelerate breakthroughs in human health? We invite you to join a leading provider of indispensable life sciences tools that is accelerating global research on multiple frontiers of human health. At Standard BioTools, we are building a positive culture where our people can do the best work of their careers, informed and influenced by our core behaviors: Keep customers front and center in all of our work Be accountable and deliver on commitments Drive continuous improvement Be collaborative and work as one team: fostering communications in a learning, coaching, and helpful environment We are currently looking for a QC Analyst to perform analytical testing of raw materials, finished product, stability samples, and R&D materials as part of the quality team. Key Job Responsibilities
Complying with cGMPs, CLIA regulations, SOPs, safety requirements, and all company policies and procedures Take ownership of and responsibility for analytical testing, including supporting method development or optimization as needed Generating and maintaining laboratory data and records in accordance with company policies Conducting product stability testing in accordance with defined schedule (per protocol) Functional analysis of material to determine binding efficiency, specificity, and other parameters as required. Testing may be performed in support of multiple working groups Analytical analysis of material to determine identity, purity, conformance to release specifications and other testing parameters Independently perform and adequately document basic investigations for out-of-specification or out-of-trend results Assisting or leading the execution / implementation of larger projects, including revising/improving test methods, SOP revisions, process improvement projects, etc. As appropriate, will cross-train in other departments or job functions to meet production or assay timelines when needed Participates in departmental or cross functional projects Qualifications
Education
Bachelor’s Degree – major in biology, chemistry, or related science is required Skills And Experience
0 - 5 years of experience in a Quality Control work environment, preferably in the pharmaceutical or medical device industries, working under cGMP or ISO regulations Ability to test raw materials, in-process materials, and finished products Experience with ELISA, microbiology, PCR, or related test methods Experience with HPLC, MS, UV-Vis, and related test methods Devise solutions for complex problems Ability to prioritize and meet deadlines, ability to multi-task effectively Learn to utilize new software as it relates to job function Strong communication and presentation skills, including technical writing and reporting Ability to build and maintain effective relationships across departments and working groups Proficient in MS Office applications, highly proficient in Excel Work Environment
Ability to work in a fast-paced environment As Somalogic is a Hazardous Waste Generator, this position performs hazardous waste duties in accordance with internal controlled documents, local, State and Federal regulations Works in a laboratory setting. The individual will be required to enter production support areas and laboratories while wearing appropriate PPE (personal protective equipment) such as lab coat, gloves and safety glasses. Note: Potential to work in proximity to patient samples, including blood, plasma, CSF, and other matrices, including known and suspected infectious material. Salary Range
$54,200 - $63,000 Annual Equal Employment Opportunity Statement
All qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status or other legally protected status.
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