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4 дня назад

Senior Analyst, Quality Control (QC Analyst)

92 500 - 120 000$
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 Analyst, Quality Control (QC Analyst) (Biotech): Performing routine and non-routine quality control sampling and testing for raw materials, in-process materials, final products, and water with an accent on GMP compliance, analytical methods, and laboratory qualification. Focus on establishing raw-material identity testing, reviewing laboratory data, validating equipment and methods, and troubleshooting analytical testing in support of production schedules.

Location: Framingham, Massachusetts, United States; 5-day on-site expectation

Salary: $92,500–$120,000 base pay annually, plus performance bonus, equity, and benefits.

Company

hirify.global develops oncolytic immunotherapies designed to activate durable systemic anti-tumor responses and transform cancer treatment.

What you will do

  • Support the setup, stocking, monitoring, and maintenance of QC laboratories and sampling areas.
  • Manage raw-material sampling and testing programs to support production schedules and material release.
  • Perform routine and non-routine testing of raw materials, in-process materials, final products, and water using established methods and SOPs.
  • Establish internal raw-material identity tests and manage qualification programs aligned with Pharmacopeia requirements.
  • Coordinate external laboratory testing, review testing data, and support method transfers, qualifications, and equipment validation.
  • Write and revise SOPs, protocols, and technical reports; support investigations, audits, inspections, and continuous improvement.

Requirements

  • BA or BS in Chemistry, Biochemistry, or a related science; additional industrial experience may substitute for degree requirements.
  • Three to five years of laboratory-based testing experience, preferably in a GMP environment.
  • Experience with product and raw-material testing and a thorough understanding of GMP raw-material testing requirements.
  • Analytical experience with techniques such as pH, conductivity, osmolality, plaque assay, ELISA, gel electrophoresis, spectroscopy, and visual inspection.
  • Computer literacy, including Microsoft Word and Excel, with strong communication and organizational skills.
  • Ability to work independently and collaboratively in a team.

Culture & Benefits

  • Mission-driven work focused on improving cancer treatment and patient outcomes.
  • Collaborative, bold, dedicated, and candid working environment.
  • Medical, dental, and vision insurance.
  • 401(k) matching, flexible time off, and paid holidays including a year-end shutdown.
  • Annual performance incentive bonus and new-hire and ongoing performance-based equity.

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