Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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$79к-132к/год
$130к$150кмедиана$180к
По похожим ролям (49) ~ $150к/год
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Хорошая вакансия
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Чётко описанная специализированная роль в крупной фармацевтической R&D-компании предлагает содержательную работу в регулируемых исследованиях и хороший пакет льгот, но предполагает работу на месте и доступна только при постоянном разрешении на работу в США.
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Понятные задачи
Крупная R&D-компания
Хорошие льготы
Требуется разрешение
Мэтч & Сопровод
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Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
DSRD Global Pathology Quality Control Scientist (Pathology): Performing independent quality control of anatomic and clinical pathology data, specimens, and reports for complex investigative, exploratory, and regulatory studies with an accent on GLP compliance, data integrity, and high-complexity pathology methods. Focus on developing and validating procedures, supporting necropsy and histology work, and ensuring reliable regulatory study reporting.
Location: Groton, Connecticut, United States; on-premise. Candidates must have permanent authorization to work in the United States; U.S. work visa sponsorship is not available.
Annual base salary: $79,400–$132,400, plus eligibility for a 7.5% bonus target.
Company
hirify.global is a pharmaceutical research and development company focused on developing therapies and vaccines that improve patients’ lives.
What you will do
Independently perform quality control of anatomic and/or clinical pathology data, specimens, and reports.
Perform regulatory responsibilities in compliance with Good Laboratory Practices and animal welfare regulations.
Support necropsy and histology procedures for complex investigative, exploratory, and regulatory studies, based on qualifications.
Develop, troubleshoot, validate, document, and refine high-complexity pathology methods, processes, assays, and reporting.
Contribute to laboratory procedures, controlled documents, publication data-integrity quality control, and pathology scheduling.
Interact with and train individuals while maintaining study-report timelines.
Requirements
Bachelor’s degree in biology or a related field with at least 6 years of experience, or a master’s degree with at least 4 years of experience.
At least 3 years of experience in a GLP environment and at least 2 years of relevant quality-control experience.
Exceptional communication skills and strong organizational change-management abilities.
Proficiency in Word, Teams, spreadsheets, PowerPoint, and relevant scientific software.
Permanent U.S. work authorization and authorization to work in the United States by any employer are required.
U.S. work visa sponsorship is not available now or in the future.
Ability to sit, stand, walk, and lift 20 pounds.
Nice to have
HT (ASCP) certification.
Master’s degree with more than 4 years of relevant experience.
Strong understanding of and adherence to regulatory guidelines.
Proficiency in VBA, .NET, SAS, SQL Server, Oracle, and MS Access, plus scripting capabilities.
Research laboratory experience.
Experience using generative AI tools such as ChatGPT or Microsoft Copilot for problem solving and productivity, with an understanding of responsible AI, risk management, and ethical use.
Culture & Benefits
Full-time, on-premise role supporting hirify.global Research and Development.
Benefits include a 401(k) with hirify.global matching and an additional retirement contribution.
Paid vacation, holidays, personal days, caregiver/parental leave, and medical leave.
Medical, prescription drug, dental, and vision coverage are provided.
Relocation assistance may be available based on business needs and eligibility.
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