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6 часов назад

Co-Op, Compliance and Data QC (Biotech)

20 - 60$
Формат работы
hybrid
Тип работы
fulltime
Грейд
trainee
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
Co-Op, Compliance and Data QC (GCLP/biotech): Supporting laboratory compliance, document control, training records, quality events, and audit readiness in a regulated clinical laboratory with an accent on data accuracy, traceability, and ALCOA+ documentation practices. Focus on organizing compliance records, tracking quality issues, preparing inspection materials, and collaborating with laboratory and compliance stakeholders.

Location: Norwood, Massachusetts, United States; 70% in-office work model. Full-time summer co-op from January 18, 2027 to June 25, 2027; candidates must be available for the entire program. Applicants must already hold US work authorization and qualify as US persons; future immigration sponsorship is not available.

Salary: $20.00–$60.00 per hour.

Company

hirify.global develops mRNA technology and medicines through a biotechnology platform and regulated laboratory operations.

What you will do

  • Support laboratory compliance activities within the CBL laboratory according to GCLP guidelines, procedures, and quality requirements.
  • Review and organize governance documents, SOPs, forms, worksheets, training records, and compliance documentation.
  • Assist with quality event and issue management through documentation, tracking, data gathering, and follow-up.
  • Support audit and inspection readiness by preparing documents, tracking requests, and organizing records.
  • Review laboratory records against good documentation practices and ALCOA+ principles.
  • Collaborate with laboratory scientists, study teams, Compliance, and cross-functional partners on quality-system projects.

Requirements

  • Currently enrolled in a bachelor's or master's STEM degree program, such as Biology, Biochemistry, Molecular Biology, Chemical Engineering, or a related field.
  • Foundational laboratory, compliance, and quality skills applicable to analytical testing.
  • Existing US work authorization that can be maintained without future sponsorship.
  • Eligibility as a US person under applicable export-control requirements.
  • Availability for the complete January 18, 2027–June 25, 2027 program.
  • Strong attention to detail, written and verbal communication, and commitment to quality.

Nice to have

  • GPA of 3.5 on a 4.0 scale or equivalent academic achievement.
  • Interest in regulated laboratory environments.
  • Ability to work independently while contributing effectively within a team.

Culture & Benefits

  • In-person collaboration, teamwork, and direct mentorship supported by a 70/30 work model.
  • Premium access to meditation and mindfulness classes.
  • Subsidized commuter benefits.
  • Paid vacation, sick time, holidays, volunteer days, and a discretionary year-end shutdown.
  • Location-specific perks and extras.

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