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9 дней назад

Process Technician Senior Coordinator (12 Month Fixed Term Contract) (Biopharma)

Формат работы
onsite
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
UK/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
Process Technician Senior Coordinator (Biopharma): Managing manufacturing and packaging processes for Botanical Drug Product batches in a regulated production environment with an accent on cGMP compliance, batch documentation, and product quality. Focus on coordinating production schedules, performing routine microbiological testing, training technicians, and implementing process improvements.

Location: Sittingbourne, UK; onsite production role with flexible working hours when production processes overrun.

Company

hirify.global is a global biopharmaceutical company developing and manufacturing medicines for serious diseases, with a focus on oncology, neuroscience, sleep disorders, and epilepsy.

What you will do

  • Manage manufacturing and packaging processes for Botanical Drug Product batches in accordance with cGMP and EH&S requirements.
  • Deliver production schedules, process batch documentation, equipment records, cleaning activities, and quality documentation.
  • Perform routine microbiological testing in the Commercial Manufacturing Suite.
  • Coordinate production activities with supply chain, warehouse, engineering, QC, and QA teams.
  • Train and coach technicians on manufacturing processes, new procedures, and process changes.
  • Identify and implement improvements that increase efficiency and reduce costs.

Requirements

  • At least 3 years of experience in a regulated production environment, ideally pharmaceutical, chemical, or food manufacturing.
  • Experience supervising or leading teams in the pharmaceutical or a related industry.
  • Knowledge of cGMP, cGxP, EH&S requirements, standard operating procedures, and quality documentation.
  • Strong attention to detail, numeracy, written and verbal communication skills, and teamwork.
  • Working knowledge of Microsoft Excel and Word.
  • Pharmaceutical industry qualifications such as NVQs or equivalent are preferred.

Culture & Benefits

  • Work in a patient-focused, science-driven biopharmaceutical environment.
  • Collaborate with internal departments and key stakeholder groups across manufacturing operations.
  • Take part in continuous improvement initiatives across production and packaging processes.
  • Fixed-term contract for 12 months with responsibilities supporting production, quality, safety, and environmental standards.

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