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13 дней назад

Process Engineer (Biopharmaceutical Manufacturing)

Формат работы
onsite
Тип работы
fulltime
Английский
b2
Страна
Spain
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:
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TL;DR
Process Engineer (Biopharmaceutical Manufacturing) (cGMP/process systems): Supporting manufacturing operations and engineering projects at a biopharmaceutical site with an accent on equipment, utilities, process improvement, qualification, and troubleshooting. Focus on leading medium-complexity projects, resolving production and quality issues, supporting tech transfer, and maintaining safe, compliant, reliable operations.

Location: Porriño, Pontevedra, Spain

Company

Global life sciences organization developing products and services that support biotechnology and biopharmaceutical manufacturing.

What you will do

  • Provide technical support for manufacturing equipment, utilities, process systems, and day-to-day site operations.
  • Identify and evaluate improvements related to safety, quality, cost, cycle time, and yield.
  • Participate in the design, implementation, commissioning, and qualification of engineering projects, including IQ activities.
  • Lead medium-complexity process engineering projects and coordinate junior engineers and contractors.
  • Troubleshoot process equipment and systems, support deviation investigations, and implement corrective and preventive actions.
  • Support technology transfer, technical documentation, and on-call manufacturing support after appropriate training.

Requirements

  • Degree or MSc in Chemical Engineering or a related engineering discipline.
  • Some relevant process engineering experience; internship or placement experience is valued.
  • Interest in biopharmaceutical manufacturing and familiarity with fluid processing equipment such as pumps, valves, piping, tanks, and transfer systems.
  • Knowledge of biopharmaceutical unit operations, including CIP/SIP, chromatography, UF/DF, bioreactors, centrifugation, HVAC, or utilities.
  • Understanding of safety and quality principles; knowledge of cGMP is an advantage.
  • Spanish and English proficiency required, with effective communication in both languages.

Culture & Benefits

  • Hands-on experience in a biopharmaceutical manufacturing environment.
  • Close collaboration with experienced engineers and cross-functional teams including Production, MSAT, Quality, and Program Management.
  • Opportunities to develop technical knowledge and contribute to engineering and process improvement projects.
  • Strong emphasis on ethical conduct, environmental responsibility, safety, and compliance.

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