gmpcloningmolecular biologyprotein purificationprotein expressionrna isolationgenomic dna
Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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$82к-102к/год
$68к$83кмедиана$97к
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Работа Company hidden над ранним выявлением рака придаёт этой лабораторной роли значимый биотехнологический фокус, а обязанности и требования описаны понятно; очный формат и редкая работа по вечерам или выходным - важные компромиссы.
Иногда по выходным
Понятные обязанности
Раннее выявление рака
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Текст:
Hirify AI/Оригинал
TL;DR
Associate Scientist 2 - Assay R&D (Molecular Biology/Protein Purification): Performing molecular biology, protein expression, purification, and analytical laboratory workflows for early cancer detection research with an accent on experimental accuracy, regulatory compliance, and reproducible documentation. Focus on executing RNA and genomic DNA isolation, cloning, fermentation, data interpretation, equipment troubleshooting, and laboratory protocol improvement.
Location: Durham, North Carolina; full-time on-site attendance required at hirify.global's Research Triangle Park laboratory
Annual base pay: $82,000–$102,000 in Durham, NC
Company
hirify.global is a healthcare company developing technologies for early cancer detection using next-generation sequencing, population-scale clinical studies, and computer and data science.
What you will do
Perform molecular biology experiments including RNA isolation, genomic DNA isolation, cDNA preparation, cloning, fermentation, protein expression, and purification.
Prepare, process, and analyze samples, reagents, buffers, and media while maintaining accurate documentation and procedural compliance.
Collect, interpret, and document experimental data in laboratory notebooks or electronic systems.
Operate, maintain, and troubleshoot laboratory equipment, escalating issues when needed.
Refine laboratory protocols, prepare technical reports and data summaries, and support quantitative analysis and project decisions.
Maintain laboratory safety, regulatory, quality, inventory, and continuous-improvement standards while providing technical guidance to junior staff.
Requirements
Bachelor’s degree in Biology, Chemistry, Biochemistry, or a related scientific discipline with 2–5 years of relevant experience, or a related master’s degree with 0–2 years of relevant experience.
Knowledge of applicable regulatory standards appropriate to the role’s complexity and scope.
Knowledge of GMP quality management systems, such as ISO 13485.
Experience or knowledge of operations in a regulated medical device environment, including IVDD, IVDR, FDA 21 CFR 800 series, and FDA 21 CFR Part 11.
Nice to have
Technical proficiency in standard laboratory techniques and equipment operation.
Ability to analyze data, identify issues, and communicate findings clearly.
Strong organizational and problem-solving skills with attention to detail.
Written and verbal communication skills, with the ability to work independently and collaboratively.
Familiarity with laboratory documentation systems, data management tools, reporting processes, laboratory safety, compliance, and quality standards.
Culture & Benefits
Work primarily takes place in a laboratory with exposure to biological, chemical, or hazardous materials; routine PPE use is required.
The role involves prolonged standing, pipetting, and handling laboratory materials, with occasional evening or weekend work when project demands require it.
Flexible time off or vacation, 401(k) with employer match, medical, dental, vision, and well-being programs are provided according to applicable plans.
The role operates under moderate supervision with periodic review of work products and outcomes.
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