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3 часа назад

Associate Manufacturing I (Biotech)

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 (Biotech): Executing and supporting biopharmaceutical plant operations in a Singapore manufacturing facility with an accent on cell culture, purification, equipment preparation, and GMP-compliant production. Focus on troubleshooting atypical process trends, performing in-process testing, supporting continuous improvement, and maintaining EHS and regulatory compliance across potentially 24/7 operations.

Location: Singapore Manufacturing - Tuas; onsite manufacturing role with availability for shifts that may include 24/7 operations.

Company

hirify.global is a biotechnology company developing, manufacturing, and delivering medicines for serious illnesses across oncology, inflammation, general medicine, and rare disease.

What you will do

  • Execute plant operations and assist with troubleshooting.
  • Monitor and analyze processing parameters for atypical trends and improvement opportunities.
  • Perform solution preparation, equipment preparation, cell culture, purification, and sterilizing filter integrity testing.
  • Stage and dispense raw materials and single-use parts, and support autoclaving, washing, and production logistics.
  • Support in-process testing of production samples and use analytical instruments.
  • Participate in continuous improvement initiatives, safety audits, inspections, and documentation review while following EHS, GMP, regulatory, and written procedures.

Requirements

  • Bachelor’s degree in science or engineering and 2 years of directly related experience, or an associate’s degree and 4 years of experience, or a high school diploma/GED in science or engineering and 6 years of experience.
  • Ability to apply basic chemistry, biology, physical principles, statistics, regulatory requirements, analytical methods, and GMP knowledge.
  • Ability to organize work, manage multiple priorities, meet deadlines, evaluate documentation and data, and interact with internal and external inspectors.
  • Ability and willingness to work any shift in support of operations that may include 24/7 coverage.
  • Medical requirements for the job scope must be fulfilled; required medical check expenses are covered by the company.

Nice to have

  • Knowledge of plant and unit operations, including autoclaves, parts washers, and process equipment.
  • Experience with Emerson DeltaV, LIMS, or TrackWise.
  • Experience with cGMP and EHS compliance in clean-room plant operations.
  • Mechanical expertise, basic computer skills, and strong problem-solving and communication skills.

Culture & Benefits

  • Collaborative, innovative, and science-based working environment.
  • Competitive base salary and comprehensive total rewards aligned with local industry standards.
  • Professional and personal growth support focused on employee well-being.
  • Inclusive workplace with reasonable accommodation available for candidates with disabilities.

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