Назад
Company hidden
7 дней назад

Engineer I – Process Engineering (Biologics Process Equipment)

Формат работы
onsite
Тип работы
fulltime
Грейд
junior
Английский
b2
Страна
Singapore
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
Engineer I – Process Engineering (Biologics Process Equipment) (Biologics Manufacturing): Supporting and owning process equipment for upstream and downstream biologics manufacturing, including equipment performance, maintenance, validation, and new product introduction with an accent on cGMP compliance, equipment readiness, and cross-functional operations. Focus on investigating equipment deviations, implementing corrective actions, maintaining validated systems, and improving reliability through data analysis and lifecycle planning.

Location: Singapore Manufacturing - Tuas; on-site

Company

hirify.global develops medicines and applies biology and technology to serve patients with serious illnesses.

What you will do

  • Own day-to-day engineering support, performance, maintenance planning, lifecycle actions, and validated state for an assigned portfolio of biologics process equipment.
  • Provide subject matter expertise for upstream and downstream equipment used in cell culture, harvest filtration, viral inactivation, purification, and drug substance bulk fill.
  • Lead equipment investigations, identify root causes, recommend corrective and preventive actions, and drive approved actions to closure.
  • Support change controls, deviations, qualifications, inspections, and equipment-readiness deliverables for new product introduction and site projects.
  • Improve equipment reliability, maintenance optimization, safety, efficiency, and operational sustainability using performance data and advanced technologies.
  • Collaborate with Manufacturing, Maintenance, Quality, Engineering, project teams, and corporate engineering on equipment design, modifications, and technical solutions.

Requirements

  • Master’s degree in Engineering, or a Bachelor’s degree with 2 years of directly related experience.
  • Alternatively, an Associate’s degree with 4 years of directly related experience, or a high school diploma/GED with 6 years of directly related experience.
  • Experience managing stakeholders and process equipment in a biopharmaceutical environment is preferred.
  • Knowledge of biopharmaceutical processes, equipment validation, qualification documentation, and critical utilities is preferred.
  • Knowledge of automation systems such as DeltaV, BMS, ladder logic, and PLC is preferred.
  • Ability to work independently, collaborate across functions, solve technical problems, and work off-hours when required.

Nice to have

  • Experience with FAT, SAT, IQ, OQ, PQ, commissioning, qualification, and system handover.
  • Project management experience covering schedules, costs, facilitation, and follow-up.
  • Knowledge of Total Productive Maintenance and Reliability Centered Maintenance.

Culture & Benefits

  • Collaborative environment focused on continuous learning and meaningful work.
  • Professional development opportunities and support for personal growth.
  • Medical checks required for the role are arranged with related expenses covered by the company.
  • Inclusive workplace committed to diversity, ethics, respect, and equal opportunity.

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 →