Назад
Company hidden
7 дней назад

Visual Inspection Manager (Biopharma)

90 000 - 130 000$
Формат работы
onsite
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
Для мэтча и отклика нужен Plus

Мэтч & Сопровод

Для мэтча с этой вакансией нужен Plus

Описание вакансии

Текст:
/
TL;DR
Visual Inspection Manager (Biopharma): Leading third-shift visual inspection operations in a regulated vaccine manufacturing environment with an accent on safety, quality, delivery, cost, and people performance. Focus on strengthening manual and automated inspection systems, leading deviation investigations, improving throughput, and developing inspection teams under cGMP and FDA requirements.

Location: Swiftwater, Pennsylvania, United States; onsite third-shift leadership role. US and Puerto Rico residents only.

Salary: $90,000–$130,000 annually

Company

hirify.global is an R&D-driven biopharmaceutical company developing medicines and vaccines through science, digital technology, and AI-powered innovation.

What you will do

  • Lead visual inspection operations during the third shift in a regulated vaccine manufacturing environment.
  • Own safety, quality, delivery, cost, and people performance while setting clear expectations and accountability.
  • Review batch records and inspection documentation and maintain inspection standards and audit readiness.
  • Lead preliminary deviation investigations, support root cause analysis, and implement corrective and preventive actions.
  • Oversee production planning, scheduling, throughput, waste reduction, process optimization, and visual inspection automation initiatives.
  • Recruit, onboard, train, coach, and manage the performance of inspectors and frontline leaders.

Requirements

  • Bachelor’s degree in any field or five years of equivalent pharmaceutical operations experience.
  • At least five years of relevant experience in pharmaceutical or biologics manufacturing.
  • At least two years of experience leading teams with direct reports.
  • Strong knowledge of cGMP requirements and quality systems, including FDA and EU Annex 1 requirements.
  • Experience driving accountability and performance improvement, including root cause investigations and corrective actions.
  • Must be available for an onsite third-shift leadership role in Swiftwater, Pennsylvania.

Nice to have

  • Direct visual inspection experience in a GMP-regulated environment.
  • Experience with manual and automated inspection processes.
  • Experience in high-volume manufacturing operations.

Culture & Benefits

  • Supportive, future-focused environment with opportunities for promotion, lateral career moves, and international development.
  • Healthcare, prevention, and wellness programs.
  • At least 14 weeks of gender-neutral parental leave.
  • Rewards package and employee benefit programs.
  • Opportunity to contribute to digital, data, AI-driven, medicine, and vaccine delivery innovation.

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 →