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4 часа назад

Manufacturing, Training and Compliance Lead (Pharmaceutical)

94 760 - 119 480$
Формат работы
onsite
Тип работы
fulltime
Грейд
lead
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

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TL;DR
Manufacturing, Training and Compliance Lead (Pharmaceutical): Coordinating floor-level training, qualification programs, and regulatory compliance activities for a site-based manufacturing facility with an accent on cGMP readiness, LMS administration, and operator competency. Focus on maintaining audit-ready training records, investigating human-error deviations, and designing CAPA training interventions across manufacturing and quality teams.

Location: Site-based at the Northbridge Manufacturing facility; travel to other manufacturing locations may be required

Salary: $94,760–$119,480 USD annually

Company

hirify.global is an ophthalmology company developing and commercializing innovative therapeutics focused on preventing blindness.

What you will do

  • Coordinate and deliver technical on-the-job training and onboarding for manufacturing technicians and operators.
  • Administer the site Learning Management System, including course assignments, completion tracking, and qualification reports.
  • Conduct performance evaluations and practical exams to certify safe and accurate operation of production equipment.
  • Monitor training matrices and review SOPs, training logs, and logbooks for alignment with shop-floor practices.
  • Support regulatory inspections by retrieving training documentation and maintaining inspection readiness.
  • Partner with Quality and Operations on root-cause investigations and implement training interventions within CAPAs.

Requirements

  • Bachelor’s degree in Engineering, Life Sciences, or a related technical field, or an equivalent combination of education and hands-on manufacturing experience.
  • At least five years of experience in a highly regulated manufacturing environment such as pharmaceutical, biotech, medical device, or aerospace.
  • At least two years in a dedicated training, compliance, or coordinator role.
  • Experience with inspection readiness initiatives and PAI inspections.
  • Ability to interpret regulatory requirements and data trends into actionable manufacturing workflows.
  • Strong communication, organizational, critical-thinking, problem-solving, and cross-functional collaboration skills.

Culture & Benefits

  • Work in a fast-paced, dynamic, high-growth environment.
  • Collaborate across Manufacturing, Quality, and Operations teams.
  • Culture emphasizes transformational innovation, integrity, compassionate excellence, and inclusive collaboration.
  • Commitment to equal opportunity, diversity, and inclusion.

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