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Secondary Packaging pMDI Supervisor (Biologics Manufacturing)

39 000
Формат работы
remote (только Italy)
Тип работы
fulltime
Грейд
middle
Английский
b2
Страна
France/Italy/Brazil
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
Secondary Packaging pMDI Supervisor (Biologics Manufacturing): Building and starting up a secondary packaging production department for a greenfield biologics manufacturing site with an accent on GMP-compliant process design, equipment qualification, and operational standards. Focus on supervising daily manufacturing, leading operators, managing deviations and investigations, and driving quality, safety, and continuous improvement.

Location: Nerviano, Milan, Italy

Salary: Minimum €39,000 per year, with the final offer based on skills, experience, qualifications, and internal equity.

Company

hirify.global is an international research-focused biopharmaceutical group operating in more than 30 countries, with over 8,000 employees and manufacturing sites in Italy, France, and Brazil.

What you will do

  • Support process and facility design, layout reviews, equipment URS definition, procurement, commissioning, and qualification for secondary packaging manufacturing lines.
  • Participate in FAT/SAT activities and help establish operational workflows for a greenfield biologics manufacturing project.
  • Develop SOPs, batch records, training programs, and operational standards in collaboration with MS&T, Engineering, QA, and Validation.
  • Supervise day-to-day secondary packaging manufacturing operations and ensure compliance with EHS, quality, GMP, and ALCOA+ requirements.
  • Lead and coach operators while monitoring production performance, deviations, investigations, and inspection readiness.
  • Drive timely resolution, continuous improvement, and a strong quality and safety culture.

Requirements

  • Degree in Biotechnology, Pharmacy, Biology, Chemical Engineering, or a related scientific discipline.
  • 3–5 years of experience in secondary packaging manufacturing.
  • Knowledge of GMP, GDP, and regulatory requirements for pharmaceutical packaging.
  • Familiarity with process validation and equipment qualification.
  • Strong documentation and deviation management capabilities.

Nice to have

  • Previous experience supervising or leading production teams.
  • Strong leadership, communication, and problem-solving skills.
  • Experience managing OEE, productivity, quality, and schedule-adherence KPIs.

Culture & Benefits

  • Purpose-driven environment focused on sustainable innovation, reliability, transparency, and ethical behaviour.
  • Comprehensive pension, private medical insurance, wellbeing, and flexible benefits programs.
  • Work-life balance initiatives, training, development resources, and performance bonuses.
  • Relocation support and tax assistance services for foreign colleagues.
  • Equal-opportunity workplace with a strong focus on diversity and inclusion.

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