Supervisor, Production (Pharmaceutical Manufacturing)
Контакты
Формат работы
onsite
Тип работы
fulltime
Грейд
lead
Английский
b2
Страна
UK
manufacturingkpigmppeople managementpharmaceutical manufacturingquality systemsroot cause analysiscleanroomcontinuous improvement
Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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Хорошая вакансия
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Чёткая руководящая роль у крупного производителя медицинской продукции с заметной ответственностью за регулируемое производство; необходимость подстраиваться под разные смены может сделать график менее предсказуемым.
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Гибкость по сменамПонятная зона ответственностиКрупный работодательРазвитие руководителя
Оценка от Hirify AI
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Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Supervisor, Production (Pharmaceutical Manufacturing): Leading multiple manufacturing teams responsible for aseptic compounding across Grade A-D cleanroom environments with an accent on GMP compliance, operational performance, and people development. Focus on optimizing production processes, investigating deviations, driving continuous improvement, and maintaining audit-ready operations.
Location: Oxford, Oxfordshire, United Kingdom. Fully site based, Monday–Friday, 9:30am–5:30pm, with flexibility required across all shifts.
Company
hirify.global develops healthcare products and operates manufacturing activities supporting patients across the UK and Ireland.
What you will do
Lead, coach, and develop Team Leaders, Deputy Team Leaders, and manufacturing associates across multiple aseptic compounding teams.
Set standards for GMP compliance, safety, performance, and operational excellence on the production floor.
Monitor production plans and operational KPIs, taking corrective action to improve results.
Collaborate with Planning, Quality, Engineering, and Logistics to meet business and customer requirements.
Optimize manufacturing processes, equipment utilization, and resource efficiency; lead continuous improvement and change control activities.
Support deviation, complaint, and root cause investigations, audit readiness, inspections, documentation, recruitment, talent development, and management cover when required.
Requirements
Proven people leadership and direct line management experience.
Experience managing end-to-end manufacturing operations in a complex production environment.
Demonstrated success leading continuous improvement, optimization, or investigational projects.
Working knowledge of GMP principles and quality systems.
Strong technical understanding of manufacturing processes and production equipment.
Experience using data and KPIs for operational decision-making and performance improvement.
Ability to inspire and motivate teams, communicate effectively at all levels, make risk-based decisions, take ownership, solve problems, manage priorities, handle conflict constructively, and build cross-functional relationships.
Commitment to diversity, inclusion, collaboration, and positive team dynamics.
Nice to have
Experience in pharmaceutical, chemical, industrial, process manufacturing, or another highly regulated industry.
Experience working in cleanroom environments.
Degree in Life Sciences, Chemical Engineering, Pharmaceutical Engineering, Process Engineering, Industrial Engineering, or a related discipline.
Culture & Benefits
Hands-on leadership role in a critical, highly regulated manufacturing operation.
Opportunity to influence operational strategy and deliver products supporting patients across the UK and Ireland.
Inclusive culture based on courage, trust, collaboration, ownership, and accountability.
Opportunity to develop leadership and technical expertise.
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