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5 дней назад

Associate Quality Control - Nights (Biotech)

62 571 - 84 656$
Формат работы
onsite
Тип работы
fulltime
Грейд
junior
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
Associate Quality Control - Nights (Biotech): Performing GMP analytical and microbiological testing in a Quality Control laboratory for manufacturing samples, raw materials, environmental monitoring, and critical utilities with an accent on time-sensitive testing, accurate documentation, and regulatory compliance. Focus on operating laboratory instrumentation, reviewing assays and records, troubleshooting deviations, and managing quality and safety risks during the Tuesday–Friday night shift.

Location: US - Rhode Island - West Greenwich; onsite night shift, Tuesday–Friday, 10 PM–8 AM

Annual salary: USD 62,571.90–84,656.10

Company

hirify.global is a biotechnology company developing, manufacturing, and delivering medicines for serious illnesses across oncology, inflammation, general medicine, and rare disease.

What you will do

  • Perform GMP analytical and microbiological testing, including titer, MMV, mycoplasma, endotoxin, bioburden, TOC, conductivity, raw material, environmental monitoring, and critical utilities testing.
  • Receive and aliquot samples and operate laboratory equipment and instrumentation.
  • Prepare complete laboratory documentation using electronic systems and laboratory notebooks.
  • Review and approve assays, documents, and records.
  • Support troubleshooting, investigations, deviations, and quality risk escalation.
  • Complete required training and perform additional quality control duties.

Requirements

  • High school diploma or GED plus 2 years of Quality experience, an associate degree plus 6 months of Quality experience, or a bachelor’s degree.
  • Experience in a GMP analytical laboratory is preferred, including analytical or biological testing based on methods or compendia.
  • Knowledge of QC analytical and quality systems, GMP principles, biopharmaceutical processes, and related unit operations is preferred.
  • Strong analytical, organizational, communication, documentation, and problem-solving skills.
  • Ability to manage multiple time-sensitive tasks independently with attention to detail and accuracy.

Culture & Benefits

  • Health, dental, vision, life, disability, and flexible spending benefits.
  • Retirement and savings plan with company contributions.
  • Annual bonus program and stock-based long-term incentives.
  • Paid time-off plans and career development opportunities.
  • Inclusive, collaborative, science-based work environment.

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