Lucence is a precision oncology company founded on a vision of a world where cancer is overcome by early detection and informed treatment. We develop advanced liquid biopsy blood tests that help physicians select suitable cancer treatments for patients by molecular profiling.
Key responsibilities:
• Monitoring clinical laboratory testing processes to ensure compliance with regulatory and state requirements.
• Maintaining accurate quality assurance and quality control records.
• Maintaining an internal audit schedule and conducting regular reviews/meetings to improve processes and quality controls.
• Organizing and hosting inspections by regulatory bodies as relevant.
• Assisting technical leads with instrument/test reviews, validations, and technical issues.
• Tracking the training and certification of employees to ensure the adequacy and competency of laboratory personnel.
• Continually staying updated on regulatory requirements and guiding laboratory personnel as relevant.
To be a good fit for this role, you would have:
• At least a Bachelor’s degree in a relevant field.
• At least two (2) years of experience working in quality assurance in a CLIA-certified laboratory.
• Familiarity with laws and regulations by CLIA, CAP, OSHA and other related legislative and/or state health departments and organizations.
• Exceptional attention to detail, being highly meticulous and organized. This is an important role in maintaining high quality standards for the laboratory.
• The ability to analyze issues critically and formulate solutions.
• The ability to work with others in a positive and collaborative manner to meet organizational goals.
Specific title may be calibrated to match a given candidate’s experience.
Interested applicants are welcome to send your CV to hr@lucence.com indicating the position you are applying for in the subject line. In addition, get creative and tell us in the email in less than 100 words (in any language you like) why you think you will be a right fit for Lucence. Don't limit yourself to a job description or job title, the world needs every skill you have.
Key responsibilities:
• Monitoring clinical laboratory testing processes to ensure compliance with regulatory and state requirements.
• Maintaining accurate quality assurance and quality control records.
• Maintaining an internal audit schedule and conducting regular reviews/meetings to improve processes and quality controls.
• Organizing and hosting inspections by regulatory bodies as relevant.
• Assisting technical leads with instrument/test reviews, validations, and technical issues.
• Tracking the training and certification of employees to ensure the adequacy and competency of laboratory personnel.
• Continually staying updated on regulatory requirements and guiding laboratory personnel as relevant.
To be a good fit for this role, you would have:
• At least a Bachelor’s degree in a relevant field.
• At least two (2) years of experience working in quality assurance in a CLIA-certified laboratory.
• Familiarity with laws and regulations by CLIA, CAP, OSHA and other related legislative and/or state health departments and organizations.
• Exceptional attention to detail, being highly meticulous and organized. This is an important role in maintaining high quality standards for the laboratory.
• The ability to analyze issues critically and formulate solutions.
• The ability to work with others in a positive and collaborative manner to meet organizational goals.
Specific title may be calibrated to match a given candidate’s experience.
Interested applicants are welcome to send your CV to hr@lucence.com indicating the position you are applying for in the subject line. In addition, get creative and tell us in the email in less than 100 words (in any language you like) why you think you will be a right fit for Lucence. Don't limit yourself to a job description or job title, the world needs every skill you have.