Назад
Company hidden
10 часов назад

Senior Principal Engineer - Process Engineering (API Manufacturing)

96 000 - 165 025
Формат работы
onsite/hybrid
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
US/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
Senior Principal Engineer - Process Engineering (API Manufacturing): Leading technical strategy and early process design for synthetic drug substance manufacturing across capital projects, technology platforms, and global manufacturing sites with an accent on API unit operations, process robustness, safety, and cGMP compliance. Focus on scaling and transferring processes, selecting manufacturing equipment, applying digital manufacturing solutions, and solving complex purification, crystallization, filtration, drying, and particle-engineering challenges.

Location: Onsite/hybrid in Geel, Belgium, or Athens, Georgia, USA; willingness to travel up to 25% domestically and internationally

Base pay: €96,000–€165,025 per year

Company

Johnson & Johnson develops healthcare solutions and medicines through its Innovative Medicine and MedTech businesses.

What you will do

  • Lead the intake, prioritization, and resolution of technical requests for synthetic drug substance manufacturing across global sites.
  • Define early-phase process designs, technology strategies, capital scopes, schedules, and equipment selections for API manufacturing.
  • Provide expertise across reactions, phase separation, distillation, crystallization, filtration, centrifugation, drying, milling, blending, and solvent recovery.
  • Drive robust, standardized, inspection-ready processes aligned with cGMP, ICH Q7, product quality, and process safety requirements.
  • Adopt real-time monitoring, advanced process control, data analytics, modeling, simulation, and smart manufacturing solutions.
  • Collaborate with R&D/CMC, MSAT, Quality, EHS, Operations, external manufacturers, and industry experts across the network.

Requirements

  • Master’s degree or equivalent experience in Engineering, Pharmaceutical Sciences, or a related technical field.
  • At least 10 years of relevant experience in synthetic drug substance or API manufacturing.
  • Expertise in API purification and solid-state or particle engineering, including crystallization, filtration, centrifugation, drying, and milling.
  • Experience with API scale-up, technology transfer, process fixing, reactor systems, solvent handling, and process analytical or control systems.
  • Strong knowledge of cGMP, API regulatory expectations, data integrity, documentation, process safety, and containment.
  • Proficiency in written and spoken English is required.

Nice to have

  • Experience with inherently safe containment for potent materials, dust control, and exposure mitigation.
  • Additional Dutch, Spanish, or Italian language skills.
  • Experience influencing cross-functional teams, external partners, and global technical decisions.

Culture & Benefits

  • Inclusive environment focused on collaboration, technical credibility, and patient impact.
  • Annual bonus based on pay grade, location, and performance.
  • Vacation, parental, bereavement, caregiver, and volunteer leave.
  • Well-being reimbursement and financial, physical, and mental health programs.
  • Insurance plans and service anniversary and recognition awards, subject to plan terms and location.

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 →