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12 дней назад

Systems Administrator, Cell Manipulation Core Facility

106 000 - 123 500$
Формат работы
hybrid
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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TL;DR
Systems Administrator, Cell Manipulation Core Facility (Clinical Laboratory Systems): Managing and validating computer systems supporting cell therapy, laboratory, manufacturing, and transfusion workflows with an accent on system integration, data integrity, and regulatory compliance. Focus on designing and maintaining internal applications, executing validation testing, securing PHI and electronic records, and coordinating complex projects across clinical and enterprise IT systems.

Location: Boston, Massachusetts, United States; hybrid with 2–3 days onsite per week, Monday–Friday, 9:00 a.m.–5:00 p.m.

Salary: $106,000–$123,500 per year

Company

hirify.global advances cancer research, treatment, education, and patient care in partnership with Harvard Medical School-affiliated hospitals.

What you will do

  • Manage, design, test, implement, and maintain systems supporting cell therapy, laboratory, manufacturing, transfusion, and clinical workflows.
  • Administer department servers, databases, interfaces, and internal applications, including FileMaker, Access, Epic, Sunquest, LIMS, MES, and environmental monitoring systems.
  • Analyze data flows and system risks, maintain business-continuity procedures, and support secure handling of critical clinical and operational data.
  • Create and execute validation plans, functional and system testing, audits, quality checks, and corrective actions for regulated systems.
  • Coordinate projects with Partners Healthcare, DFCI Information Services, vendors, programmers, and clinical or laboratory stakeholders.
  • Develop training materials, conduct end-user training, generate compliance reports, and support CIBMTR data submissions.

Requirements

  • Bachelor’s degree in a relevant field and at least five years of experience in a blood bank or cGMP laboratory, plus five years of systems experience.
  • Knowledge of cell therapy, laboratory workflows, medical terminology, PHI compliance, validated systems, and networked computer systems.
  • Experience with FileMaker Pro, Microsoft applications, Excel pivot tables, OneDrive, SharePoint, Teams, Rees, MasterControl, Eceptionist, BOE/BPAA, Sunquest, Epic, LIMS, and MES.
  • Working knowledge of SQL or another relevant programming language, scripting, reporting, ODBC/JDBC interfaces, and complex IT architecture data flows.
  • Ability to write and execute validation plans and testing documentation aligned with DQ, IQ, OQ, and performance qualification requirements.
  • Knowledge of 21 CFR Part 11, cGDP, HIPAA, FACT, Joint Commission, ISO 27001/27002, NIST, OWASP, and CIS security standards.

Nice to have

  • Project management certification.

Culture & Benefits

  • Hybrid work arrangement with required onsite presence in Boston.
  • Inclusive, diverse, and equitable environment focused on compassionate patient care.
  • Opportunity to support cancer research, clinical operations, and public health programs.
  • Schedule may require occasional off-shift or weekend assignments based on workload.

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