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6 дней назад

Equipment Engineer Parenteral Pilot Plant (Pharmaceutical)

72 500 - 115 230€
Формат работы
onsite
Тип работы
fulltime
Английский
b2
Страна
Belgium
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
Equipment Engineer Parenteral Pilot Plant (Pharmaceutical) (parenteral manufacturing equipment and GMP qualification): Developing and improving equipment for clinical pharmaceutical manufacturing in a regulated pilot plant with an accent on equipment design, qualification, sterilization systems, and process performance. Focus on leading equipment investment projects, creating URS and qualification documentation, supporting FAT/SAT activities, and solving technical and process risks through HAZOP and FMEA.

Location: Beerse, Antwerp, Belgium; the role is based in Beerse.

Base pay: €72,500–€115,230 annually.

Company

Johnson & Johnson MedTech develops healthcare and pharmaceutical solutions, including medicines and medical technologies.

What you will do

  • Develop technical expertise in parenteral manufacturing equipment, including processors, fill-finish equipment, autoclaves, dry heat ovens, sterilize-in-place systems, lyophilizers, and nano-milling equipment.
  • Translate process and user needs into technical solutions, identify improvement opportunities, and troubleshoot existing equipment.
  • Support technical, quality, safety, and process risk assessments, including HAZOP, SWIFT, and FMEA.
  • Create and approve lifecycle and qualification documentation, including URS, risk assessments, IOPQ, deviations, and change controls.
  • Lead and support investment projects from concept through design, supplier selection, installation, commissioning, start-up, and qualification.
  • Coordinate multidisciplinary project teams and support FAT, SAT, feasibility studies, capacity analyses, and business cases.

Requirements

  • Master’s degree in engineering or equivalent relevant experience.
  • Experience in equipment engineering, manufacturing, or technical project delivery in a regulated pharmaceutical, food, or chemical environment.
  • Understanding of engineering principles, equipment design standards, GMP, equipment qualification, automation, and data integrity.
  • Knowledge of machinery safety, ATEX, piping standards, HAZOP, or FMEA.
  • Experience with project management methods and planning tools such as FPX and Microsoft Project.
  • Professional proficiency in English and Dutch is required.

Nice to have

  • Experience with business case modeling, feasibility studies, mechanical engineering, product development, or SAP Product Lifecycle Management.
  • Experience with technical writing, supplier collaboration, design reviews, or acceptance testing.

Culture & Benefits

  • Work in a global development matrix organization with internal specialists, suppliers, operators, engineers, quality partners, and safety specialists.
  • Three-year fixed-term role with training, supplier contact, peer learning, and hands-on development opportunities.
  • Annual bonus based on pay grade, location, and employee and company performance.
  • Vacation, parental leave of at least 12 weeks, bereavement, caregiver, and volunteer leave.
  • Well-being reimbursement and programs supporting financial, physical, and mental health, plus eligible insurance plans and recognition awards.

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