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Manufacturing Expansion Transition Technician – A Shift (Pharmaceutical Manufacturing)

Формат работы
onsite
Тип работы
project
Английский
b2
Страна
UK
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
Manufacturing Expansion Transition Technician – A Shift (Pharmaceutical Manufacturing): Supporting production continuity in legacy pharmaceutical manufacturing suites during a two-year manufacturing expansion transition with an accent on GMP compliance, equipment operation, quality documentation, and shift-based production. Focus on operating and maintaining production equipment, supporting validation and root-cause investigations, reducing downtime, and delivering continuous-improvement activities such as Kaizen, 5S, and autonomous maintenance.

Location: GB Cambridge, Bard Manufacturing Facility; onsite, shift-based manufacturing work

Company

hirify.global’s Bard facility manufactures medicines with a focus on operational excellence, quality, compliance, and reliable patient supply.

What you will do

  • Support Cell Leads in delivering daily production targets within assigned legacy manufacturing areas.
  • Prepare, operate, clean, inspect, and maintain manufacturing equipment and production areas.
  • Maintain production continuity, complete shift handovers, and escalate issues affecting output or product quality.
  • Contribute to root-cause investigations, validation activities, troubleshooting, and equipment reliability initiatives.
  • Support continuous-improvement work, including Kaizen, 5S, waste reduction, yield improvement, and autonomous maintenance.
  • Complete production documentation accurately and maintain GMP, Health & Safety, security, and environmental compliance.

Requirements

  • Minimum of 4 GCSEs at Grade C / Level 4 or above, including Mathematics and English, or equivalent qualifications.
  • Practical aptitude, reliability, flexibility, attention to detail, and willingness to learn; full training is provided.
  • Ability to work in a physically demanding manufacturing environment with manual handling, equipment changeovers, PPE, RPE, cleaning chemicals, and pharmaceutical active ingredients.
  • Ability to work shifts and commit to the full two-year fixed-term contract.
  • Knowledge of GMP, 5S, Kaizen, continuous improvement, TPM, equipment care, documentation, and regulatory compliance.
  • Experience in GMP manufacturing, pharmaceutical production, equipment operation, maintenance, quality, or validation is desirable but not essential.

Nice to have

  • A-Levels or an equivalent vocational qualification.
  • Approximately two years of manufacturing, production, engineering, mechanical, or related operational experience.
  • Pharmaceutical manufacturing experience or knowledge of process equipment maintenance.
  • Practical or mechanical interests, such as vehicle maintenance, car mechanics, or engineering hobbies.

Culture & Benefits

  • Competitive salary, shift allowance or pay, and a flexible benefits package.
  • Full training and development in practical, technical, and GMP manufacturing skills.
  • Experience within a highly regulated pharmaceutical manufacturing environment.
  • Supportive, collaborative, and inclusive workplace focused on safety, quality, teamwork, and continuous improvement.
  • Opportunity to support a major manufacturing transformation programme and continuity of patient supply.

Hiring process

  • Successful candidates receive full training for the assigned legacy manufacturing operations.
  • The role does not include training, qualification, authorization, or deployment on the new ADHD bead manufacturing unit or expansion assets.

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