Назад
Company hidden
5 дней назад

Associate Quality Control (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
Для мэтча и отклика нужен Plus

Мэтч & Сопровод

Для мэтча с этой вакансией нужен Plus

Описание вакансии

Текст:
/
TL;DR
Associate Quality Control (Biotech) (cGMP laboratory testing): Executing and reviewing analytical testing of raw materials using HPLC, GC, ICPMS, and wet chemistry methods with an accent on regulatory compliance, accurate documentation, and laboratory operations. Focus on reviewing assays and records, participating in investigations, identifying quality and safety risks, and supporting continual improvement in a pharmaceutical manufacturing network.

Location: US - Rhode Island - West Greenwich; onsite laboratory role based at hirify.global Rhode Island

Salary: $62,571.90–$84,656.10 annual

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

  • Execute and review analytical testing of raw materials in a cGMP laboratory.
  • Operate laboratory equipment and instrumentation, including HPLC, GC, and ICPMS systems.
  • Prepare complete and accurate laboratory documentation using electronic systems and laboratory notebooks.
  • Review and approve assays, documents, and records while ensuring compliance with cGMP and other regulations.
  • Participate in laboratory investigations, continual improvement initiatives, and quality, compliance, supply, and safety risk escalation.
  • Maintain laboratory housekeeping and complete required training.

Requirements

  • High school diploma or GED plus 2 years of Quality or Operations experience, or an Associate’s degree plus 6 months of Quality or Operations experience, or a Bachelor’s degree.
  • Experience or knowledge in laboratory practices, preferably in a fast-paced GxP laboratory.
  • Ability to manage multiple tasks, remain adaptable, and work effectively with supervision.
  • Knowledge of USP and PhEUR pharmacopeial testing is preferred.
  • Experience with benchtop wet chemistry, titrations, HPLC, or GC is preferred.

Culture & Benefits

  • Collaborative, innovative, and science-based work environment.
  • Health, dental, vision, life, disability, and flexible spending benefits for eligible employees and dependents.
  • Retirement and savings plan with company contributions.
  • Discretionary annual bonus, stock-based long-term incentives, and award-winning time-off plans.
  • Career development and work-life balance support.

Hiring process

  • Applications are accepted until a candidate is selected or a sufficient number of applications is received.
  • Sponsorship for this role is not guaranteed.

Будьте осторожны: если работодатель просит войти в их систему, используя iCloud/Google, прислать код/пароль, запустить код/ПО, не делайте этого - это мошенники. Обязательно жмите "Пожаловаться" или пишите в поддержку. Подробнее в гайде →