Назад
Company hidden
9 дней назад

Scientific Principal Engineer (Manufacturing Sciences and Technology)

79 800 - 137 770€
Формат работы
onsite
Тип работы
fulltime
Грейд
senior
Английский
c1
Страна
Belgium
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
Для мэтча и отклика нужен Plus

Мэтч & Сопровод

Для мэтча с этой вакансией нужен Plus

Описание вакансии

Текст:
/
TL;DR
Scientific Principal Engineer (Manufacturing Sciences and Technology): Managing clinical manufacturing activities for synthetic-molecule drug products across internal pilot plants and external CMO networks with an accent on oral solid, liquid, and parenteral processes. Focus on leading drug product process introduction, manufacturing readiness, scale-up and technology transfer, and solving complex GMP-regulated development challenges across global cross-functional teams.

Location: Beerse, Antwerp, Belgium; onsite work at the Drug Product Pilot Plant. Willingness to travel up to 5% of the time is required.

Base pay: €79,800–€137,770 per year, plus bonus and benefits.

Company

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

What you will do

  • Manage clinical manufacturing activities for synthetic-molecule drug products in the internal pilot plant and external CMO network.
  • Represent Pharmaceutical Supply and Engineering Sciences in drug product development and clinical supply chain teams.
  • Lead lean, right-first-time process introduction and manufacturing readiness for pilot-plant and CMO operations.
  • Coordinate scale-up and technology-transfer preparation from pilot-plant processes to commercial manufacturing facilities.
  • Own relationships with one or more external CMOs, project critical paths, risks, corrective actions, and dedicated budgets.
  • Establish and review manufacturing instructions and specifications while improving workflows and process-development operations.

Requirements

  • MSc or PhD in chemistry, pharmaceutical sciences, biochemical or mechanical engineering, or a related pharmaceutical or biotechnology discipline.
  • At least 10 years of experience in GMP-regulated pharmaceutical development or engineering.
  • Experience with oral solid dosage, liquid, and/or parenteral manufacturing, including technologies such as spray drying, extrusion, and continuous manufacturing.
  • Knowledge of regulated environments, FDA standards, GMP guidelines, risk management, qualification, validation, and change management.
  • Strong coordination, collaboration, influencing, communication, and organizational skills, with the ability to work independently under challenging timelines.
  • Fluent English, written and spoken, is required.

Nice to have

  • Basic understanding of process analytical technologies and advanced data science tools.
  • Proficiency in Dutch.
  • Experience with innovative pilot-plant manufacturing platforms and SAP Product Lifecycle Management.

Culture & Benefits

  • International, cross-functional environment focused on continuous learning and professional growth.
  • On-site sports facilities, health programs, and family benefits.
  • Vacation days, parental leave of at least 12 weeks, bereavement, caregiver, and volunteer leave.
  • Well-being reimbursement and programs supporting financial, physical, and mental health.
  • Annual bonus, insurance plans where applicable, service anniversary awards, and recognition programs.

Будьте осторожны: если работодатель просит войти в их систему, используя iCloud/Google, прислать код/пароль, запустить код/ПО, не делайте этого - это мошенники. Обязательно жмите "Пожаловаться" или пишите в поддержку. Подробнее в гайде →