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SENIOR QC ASSOCIATE

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Company :
ChromaCode

Location :
Carlsbad, California

Expiry Date :
Mon, 21 Dec 2020 23:59:59 GMT

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Description :
Job Details Full-timeEstimated: $56,000 – $78,000 a year4 hours ago Qualifications – Analysis skills – Math – Laboratory experience – Spectrophotometer – Communication skills – Bachelor’s degree Full Job Description We are seeking a highly motivated individual to join our reagent manufacturing team. The qualified candidate is expected to perform testing of PCR reagents as well as drive NCRs and Deviations to completion. itional responsibilities include drafting procedures, preparing protocols for experiments of simple to moderate complexity with minimal supervision, preparing technical reports, and summaries of assigned projects. Must be comfortable performing bench work, and in self-direction of work plans and procedures. Who we are: We are a fast-growing life sciences tools company, passionate about increasing the performance of molecular diagnostics instruments to drive better decision-making. We are currently using our HDPCR technology to deliver some of the best diagnostic testing solutions for COVID-19. You will join a team of highly talented people in a well-funded, exciting environment. What you will be responsible for: Work within a cGMP production-based pipeline Complete all Production and QC testing as scheduled Lead quality investigations, root cause analysis, corrective actions, preventive actions, and support quality system continuous improvement Create and revise QC documentation Strictly adhere to established policies and procedures for reagent manufacturing and quality control; report any problems with documentation Troubleshoot technical challenges in both production and testing of products Interface with members in manufacturing and product development to understand new methods pertaining to testing All other reasonable tasks as may be requested by supervisor Your ideal qualifications: Requires a Bachelor’s degree in Biology or related field with 3+ years of relevant work experience in Biotech industry Highly experienced in the laboratory, including use of pipettes, scales, centrifuge, spectrophotometer, and PCR instrumentation Proficiency in PCR and data analysis is required Ability to effectively communicate technical results, formulate options and interface with R & D, and manufacturing Self-motivated, hard-working, detail-oriented and able to work in a fast-paced team environment with demonstrated problem solving skills. Excellent time/task management skills with an ability to work independently and manage numerous tasks at once Excellent math skills, strong organizational skills, and very detail oriented. Familiar with cGMP, ISO9000/13485, product specifications incoming inspection procedures. Effective verbal and written communication, analytical, and interpersonal skills. If interested, please email resume and cover letter describing your qualifications to: ChromaCode believes that everyone has the ability to make an impact, and we are proud to be an equal opportunity employer committed to providing employment opportunity regardless of sex, race, creed, color, gender, religion, marital status, domestic partner status, age, national origin or ancestry, physical or mental disability, medical condition, sexual orientation, pregnancy, military or veteran status, citizenship status, and genetic information. If you have a disability or special need that requires accommodation, please contact us at . To learn more, visit: Show full job description Quick