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3 дня назад

Senior Associate Quality Assurance (Biotech)

82 081 - 111 052$
Формат работы
onsite
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
Senior Associate Quality Assurance (Biotech): Sampling and inspecting raw materials and components, reviewing quality documentation, and maintaining sampling equipment in a fully onsite biopharmaceutical manufacturing environment with an accent on GMP practices, inspection accuracy, and safe handling of chemicals and large drums. Focus on leading continuous improvement projects, operating warehouse and inspection equipment, and solving documentation and sampling challenges while meeting quality and safety requirements.

Location: Fully onsite in Thousand Oaks, California, United States

Salary: $82,081.95–$111,052.05 annual base salary

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

  • Sample and inspect raw materials and components, primarily chemicals.
  • Review quality documentation for assigned functions, including equipment and maintenance records.
  • Lead small projects and continuous improvement initiatives.
  • Operate and maintain sampling instruments and equipment, including balances, drum lifts, and pallet jacks.
  • Maintain training records and record and calculate quality data.
  • Work independently and collaboratively while applying safety, sampling, and inspection procedures.

Requirements

  • High school diploma or GED with 4 years of Quality experience, an associate degree with 2 years of Quality experience, or a bachelor’s degree with 6 months of Quality or Operations experience; a master’s degree is also listed as qualifying.
  • Ability to work fully onsite in Thousand Oaks, California.
  • Ability to lift and maneuver 30+ pounds, including drums weighing 50+ pounds, and pass a vision assessment for inspection work.
  • Understanding of aseptic techniques, cGMPs, gowning, sampling procedures, and safety guidelines.
  • Strong written and verbal communication, attention to detail, time management, basic problem-solving, and computer skills.
  • Comfort working with raw materials and components and spending extended periods in the sampling suite.

Nice to have

  • Bachelor’s degree.
  • Prior GMP experience.
  • Experience using production or warehouse equipment.
  • Familiarity with inspection equipment.

Culture & Benefits

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

Hiring process

  • Applications are accepted until a sufficient number of candidates is received or a candidate is selected.
  • Sponsorship is not guaranteed.

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