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Supervisor Engineering Supervisor - Quality Control (Pharma Laboratory)

72 400 - 108 600
Формат работы
onsite
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
Ireland
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
Supervisor Engineering Supervisor - Quality Control (Pharma Laboratory) (Pharmaceutical Quality Control): Leading quality control laboratory operations and batch release support for pharmaceutical combination products with an accent on cGMP compliance, analytical testing, and laboratory performance. Focus on developing laboratory personnel, supporting method validation and transfer, maintaining data integrity, and driving continuous improvement in a regulated manufacturing environment.

Location: Galway, County Galway, Ireland; full-time, with no remote or hybrid arrangement stated.

Salary: €72,400–€108,600 per year, plus eligibility for the hirify.global Incentive Plan short-term incentive.

Company

hirify.global develops healthcare technologies and pharmaceutical combination products designed to improve patient health and support the product lifecycle.

What you will do

  • Supervise daily Quality Control laboratory operations and ensure compliance with regulatory and company requirements.
  • Lead, coach, train, and develop laboratory personnel, including performance management and succession planning.
  • Oversee accurate testing, raw data, laboratory records, analytical results, and timely reporting.
  • Support production schedules, operational planning, batch release, and business continuity.
  • Collaborate with Quality Assurance, Manufacturing, and other stakeholders to maintain the Quality Management System.
  • Support method development, validation, transfer, scientific studies, and continuous improvement initiatives.

Requirements

  • Bachelor’s degree in Chemistry or a related scientific discipline with 3+ years of pharmaceutical Quality Control laboratory experience, including supervisory or people leadership responsibilities; alternatively, an advanced degree with at least 1 year of relevant experience.
  • Knowledge of pharmaceutical manufacturing, cGMP, USP, FDA, and ICH guidance.
  • Experience with Quality Control testing and laboratory operations in a regulated pharmaceutical environment.
  • Experience with laboratory documentation, data integrity, and Quality Management Systems.
  • Ability to lead teams, prioritize workload, and support operational objectives in a manufacturing environment.

Nice to have

  • Experience with HPLC, GC, dissolution, FTIR, UV/Vis spectroscopy, and wet chemistry methods.
  • Experience with method validation, method transfer, and compendial verification.
  • Experience supporting laboratory investigations, deviations, CAPA, and continuous improvement programs.
  • Background in pharmaceutical, combination product, or medical device manufacturing.
  • Knowledge of batch release and product quality oversight.

Culture & Benefits

  • Competitive salary and flexible benefits package.
  • Short-term incentive eligibility through the hirify.global Incentive Plan.
  • Benefits and resources designed to support employees across career and life stages.
  • Work in a healthcare technology organization focused on patient outcomes and product quality.

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