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4 дня назад

Pharmaceutical Compliance Specialist (Pharma)

26 - 30$
Формат работы
onsite
Тип работы
fulltime
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
Pharmaceutical Compliance Specialist (GMP/Quality Systems): Developing and monitoring quality metrics, investigations, training reports, and improvement activities in a GMP-regulated pharmaceutical environment with an accent on cGMP, FDA requirements, and cross-functional quality oversight. Focus on analyzing quality trends, managing CAPA and audit-related activities, evaluating training effectiveness, and maintaining compliance with internal procedures.

Location: Rensselaer, New York, USA; onsite, Monday-Friday, 8:00 AM-4:30 PM

Salary: $26.25-$30.00 per hour

Company

Eurofins PSS provides analytical testing and scientific services for pharmaceutical, medical device, food, cosmetic, and consumer products companies through an international laboratory network.

What you will do

  • Develop quality metrics, KPIs, measurable objectives, and regular investigation and training reports.
  • Collect and analyze process, defect, and performance data to identify trends and improvement opportunities.
  • Collaborate with client Quality stakeholders and cross-functional PSS site teams.
  • Manage quality improvement activities, meetings, workflow, resources, and cross-functional training.
  • Support GMP-regulated quality activities and continuous improvement aligned with FDA requirements.
  • Provide oversight of quality systems, policies, procedures, documentation, and training effectiveness.

Requirements

  • Bachelor’s degree plus 2 years of relevant industry experience, or a master’s degree in Pharmacy, Biology, Chemistry, or a related scientific field plus 1 year of relevant experience.
  • Experience with quality investigations, deviations, audits, CAPAs, quality management systems, or controlled document storage.
  • Pharmaceutical industry and manufacturing operations experience.
  • Strong knowledge of global regulatory requirements, cGMP, and industry best practices.
  • Strong technical writing and communication skills.
  • Ability to work onsite in Rensselaer, New York, during the stated Monday-Friday schedule.

Culture & Benefits

  • Full-time employment with medical, dental, and vision coverage.
  • Life and disability insurance.
  • 401(k) with company match.
  • Paid vacation and holidays.
  • Potential yearly bonus and merit-based pay increases.

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