Назад
Company hidden
7 дней назад

Senior Quality Compliance Specialist (CVRM)

94 000 - 174 600$
Формат работы
onsite
Тип работы
fulltime
Грейд
senior
Английский
c1
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

Senior Quality Compliance Specialist (CVRM): Leading the design and implementation of Quality Risk Management and Data Integrity initiatives for a new high-volume drug manufacturing facility with an accent on risk-based operational controls and GxP compliance. Focus on chairing the Change Review Board, ensuring data integrity in automated systems, and fostering a proactive quality culture during the site's ramp-up phase.

Location: Must be based in Holly Springs, North Carolina

Salary: $94,000–$174,600

Company

hirify.global, a member of the Roche group, is a pioneer in the biotechnology industry dedicated to developing groundbreaking medicines for serious and life-threatening diseases.

What you will do

  • Lead the site's Quality Risk Management (QRM) program, facilitating complex risk assessments using methodologies like FMEA and PHA.
  • Take full ownership of the Data Integrity program, ensuring compliance for all automated, digital, and analytical systems.
  • Chair the site Change Review Board to evaluate and approve high-impact modifications during commissioning and validation.
  • Provide technical leadership to resolve compliance issues and support core quality systems including inspections and supplier management.
  • Partner cross-functionally with Engineering, Operations, and Global teams to integrate risk-based principles into operational design.

Requirements

  • Bachelor's degree in a scientific or technical discipline required.
  • Minimum 8–10 years of experience in a GxP environment.
  • At least 4 years of experience leading QRM, Data Integrity, or Change Control programs in manufacturing.
  • Deep knowledge of global GxP regulations (FDA, EMA, ICH, ISO) for sterile drug product manufacturing.
  • Proven success in auditing or implementing site-wide Data Integrity programs in highly automated facilities.
  • Must be able to work onsite in Holly Springs, NC; relocation assistance is not available.

Culture & Benefits

  • Opportunity to launch a state-of-the-art $2B greenfield manufacturing facility from the ground up.
  • Work in a fast-paced, entrepreneurial environment focused on next-generation metabolic medicines.
  • Comprehensive benefits package including health insurance and retirement plans.
  • Commitment to a culture of transparency, solution-oriented dialogue, and operational excellence.

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 →