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1 день назад

Senior Manager, Packaging Engineering (Biotech)

Формат работы
onsite
Тип работы
fulltime
Грейд
senior
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
Senior Manager, Packaging Engineering (Biotech): Establishing a new labeling and secondary packaging operation at Moderna’s Harwell site with an accent on technical leadership, GMP compliance, equipment qualification, and maintenance strategy. Focus on commissioning and validating packaging systems, solving complex equipment issues, and building a high-performing engineering and maintenance function.

Location: Oxford, England; site-based work at the Harwell facility

Company

hirify.global develops mRNA technology and medicines through a science-driven biotechnology platform.

What you will do

  • Lead the development and implementation of labeling and secondary packaging equipment for the Harwell site.
  • Provide technical leadership across capital projects from conceptual design through commissioning, qualification, and validation.
  • Develop engineering documentation, including URS inputs, design specifications, process parameters, FMEA, turnover packages, equipment specifications, manuals, and drawings.
  • Troubleshoot complex equipment failures and coordinate internal teams, external vendors, and engineering consultants.
  • Build the site maintenance strategy, including preventive maintenance plans, spare-parts strategies, equipment criticality assessments, and job plans.
  • Lead continuous improvement, shutdown, CAPEX, compliance, and engineering business-process initiatives while developing the long-term maintenance capability.

Requirements

  • Bachelor’s or Master’s degree, preferably in Packaging, Mechanical, or Automation Engineering; other engineering degrees will be considered.
  • At least 8 years of relevant experience as a Packaging Engineer.
  • Strong technical and regulatory knowledge of labeling and secondary packaging requirements in the pharmaceutical or biotechnology industry.
  • Experience with GMP environments, capital or expansion programs, and direct design responsibility.
  • Experience with thermoforming, heat sealing, cartoning, flexible packaging lines, vision inspection, serialization, barcode printing and verification, and coding systems.
  • Strong communication, technical writing, structured problem-solving, root-cause analysis, and ability to manage multiple complex assignments.

Nice to have

  • Working knowledge of automatic inspection and clinical packaging operations.
  • Basic statistical analysis skills.
  • Experience with Excel, Word, and PowerPoint.

Culture & Benefits

  • In-person collaboration supported through a 70/30 work model with 70% of work conducted in the office.
  • Healthcare and voluntary benefit programs.
  • Fitness, mindfulness, and mental-health support.
  • Family-building benefits, including fertility, adoption, and surrogacy support.
  • Paid time off, bank holidays, volunteer days, sabbatical, global recharge days, and a discretionary year-end shutdown.
  • Savings and investment programs, plus location-specific benefits.

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