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5 дней назад

Associate Manufacturing I (Biotechnology)

Формат работы
onsite
Тип работы
fulltime
Грейд
junior
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
Associate Manufacturing I (Biotechnology): Executing plant operations for biopharmaceutical manufacturing in a classified cleanroom with an accent on equipment preparation, material staging, environmental monitoring, and GMP compliance. Focus on analyzing process trends, troubleshooting production activities, supporting continuous improvement, and maintaining safe, accurate operations across 24/7 shifts.

Location: Singapore Manufacturing - Tuas; onsite

Company

hirify.global is a biotechnology company developing, manufacturing, and delivering medicines for serious illnesses.

What you will do

  • Execute plant operations and assist Manufacturing Associates with troubleshooting.
  • Monitor processing parameters, identify atypical trends, and support continuous improvement initiatives.
  • Prepare solutions and equipment, stage and dispense raw materials and single-use parts, and support autoclaving and washing activities.
  • Perform sterilizing filter integrity testing, environmental monitoring of classified cleanrooms, and in-process production sample testing.
  • Support safety audits, follow EHS and regulatory requirements, evaluate documentation and data, and interact with internal and external inspectors.
  • Perform physically demanding production-floor activities, including standing for extended periods and lifting, carrying, pushing, or pulling items weighing under 12 kg.

Requirements

  • Bachelor’s degree with 2 years of directly related experience, an associate degree with 4 years, or a high school diploma/GED with 6 years; fresh graduates may be considered.
  • 0–2 years of relevant experience in biotechnology, pharmaceutical, or petrochemical manufacturing.
  • Knowledge of plant and unit operations, including autoclaves, parts washers, and process equipment, with strong problem-solving and mechanical skills.
  • Understanding of cGMP, EHS compliance, cleanroom operations, basic chemistry, biology, physical principles, regulatory requirements, and analytical methods.
  • Experience with Emerson DeltaV, LIMS, and TrackWise; basic computer skills with Microsoft Office, email, and learning management systems.
  • Willingness to work any shift, including schedules supporting 24/7 operations. Medical requirements for the role must also be fulfilled.

Culture & Benefits

  • Collaborative, innovative, and science-based work environment.
  • Competitive base salary and comprehensive total rewards aligned with local industry standards.
  • Company-covered expenses for required medical checks.
  • Inclusive workplace focused on professional growth, well-being, and equal opportunity.

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