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4 дня назад

Senior Process Engineer (Pharmaceutical)

Формат работы
onsite
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
Singapore
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
Senior Process Engineer (Pharmaceutical) (pharmaceutical manufacturing): Providing process engineering support for pharmaceutical and biopharmaceutical manufacturing, including process design, equipment qualification, automation changes, and continuous improvement with an accent on safe, reliable, and efficient site operations. Focus on developing engineering documentation, leading change controls and CAPAs, translating process requirements into automation modules and recipes, and troubleshooting validated process systems.

Location: Singapore — permanent, onsite role.

Company

hirify.global is an independent technology consulting firm delivering solutions across Information System & Digital, Telecom, Life Sciences, and Engineering.

What you will do

  • Develop process designs, P&IDs, URS, risk assessments, and lifecycle engineering documentation.
  • Participate in design reviews, design qualification, HAZOP studies, FAT, SAT, IQ, OQ, PQ, requalification, and validation activities.
  • Own process systems and equipment including SIP, CIP, washers, and autoclaves.
  • Lead change controls, deviations, investigations, CAPAs, troubleshooting, and engineering improvements.
  • Translate process requirements into automation equipment modules, recipes, and parameters, and support recipe testing.
  • Provide independent technical and on-call support for safe, reliable, and efficient site operations.

Requirements

  • Degree in Chemical Engineering, Process Engineering, Pharmaceutical Engineering, Biotechnology, Mechanical Engineering, or a related field.
  • 5–8 years of process engineering experience in pharmaceutical, biopharmaceutical, biotechnology, or similarly regulated manufacturing.
  • Experience with process design, P&IDs, URS, risk assessments, design reviews, and HAZOP.
  • Knowledge of qualification and validation activities, including FAT, SAT, IQ, OQ, PQ, and requalification.
  • Practical experience with CIP, SIP, washers, autoclaves, or comparable pharmaceutical process systems.
  • Experience with automated manufacturing processes, change controls, deviations, investigations, CAPAs, and cross-functional collaboration.

Culture & Benefits

  • International community representing more than 110 nationalities.
  • Internal Academy with more than 250 training modules.
  • Opportunities to lead sustainability and ESG initiatives through the WeCare Together program.
  • Regular internal events including afterworks and team-building activities.

Hiring process

  • Brief virtual or phone call.
  • Approximately three interviews, varying by seniority.
  • Potential case study, technical assessment, role play, or problem-solving exercise.

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