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3 дня назад

Biotechnologist, MFG (MM)

Π€ΠΎΡ€ΠΌΠ°Ρ‚ Ρ€Π°Π±ΠΎΡ‚Ρ‹
onsite
Π’ΠΈΠΏ Ρ€Π°Π±ΠΎΡ‚Ρ‹
fulltime
Английский
b2
Π‘Ρ‚Ρ€Π°Π½Π°
Singapore
Вакансия ΠΈΠ· списка Hirify.GlobalВакансия ΠΈΠ· Hirify Global, списка ΠΌΠ΅ΠΆΠ΄ΡƒΠ½Π°Ρ€ΠΎΠ΄Π½Ρ‹Ρ… tech-ΠΊΠΎΠΌΠΏΠ°Π½ΠΈΠΉ
Для мэтча ΠΈ ΠΎΡ‚ΠΊΠ»ΠΈΠΊΠ° Π½ΡƒΠΆΠ΅Π½ Plus

ΠœΡΡ‚Ρ‡ & Π‘ΠΎΠΏΡ€ΠΎΠ²ΠΎΠ΄

Для мэтча с этой вакансиСй Π½ΡƒΠΆΠ΅Π½ Plus

ОписаниС вакансии

ВСкст:
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TL;DR
Biotechnologist, MFG (MM) (Biotechnology): Preparing materials, equipment, and cleanroom areas for cGMP manufacture of therapeutic proteins with an accent on aseptic operations, laboratory measurements, compliant documentation, and manufacturing equipment readiness. Focus on executing batch records and SOPs, operating DeltaV and LIMS workflows, supporting deviations and validation activities, and troubleshooting production issues during rotating 12-hour shifts.

Location: Tuas, Singapore; onsite manufacturing role with rotating 12-hour shifts

Company

hirify.global manufactures medicines and therapeutic products across a globally connected network of more than 30 sites on five continents.

What you will do

  • Prepare materials, equipment, and manufacturing areas for cGMP production of therapeutic proteins.
  • Maintain cleanroom areas and equipment through sanitization, 6S housekeeping, suite stocking, and Kanban activities.
  • Perform sampling and basic laboratory measurements, including pH, conductivity, and osmolality testing, using aseptic techniques.
  • Execute manufacturing activities with SOPs, batch records, logbooks, and LIMS while maintaining accurate documentation.
  • Build competency in manufacturing equipment, critical process parameters, DeltaV operations, and batch or changeover workflows.
  • Support deviations, environmental monitoring, document revisions, validation, data integrity, and cross-functional troubleshooting with Manufacturing, MSAT, and QA.

Requirements

  • Diploma, NITEC, or degree in Biotechnology, Biochemistry, Chemical or Biochemical Engineering, Life Sciences, Engineering, or a related discipline.
  • Relevant pharmaceutical, biopharmaceutical, manufacturing, or cleanroom operations experience is preferred; relevant technical training is also considered.
  • Basic understanding of cGMP requirements, manufacturing procedures, and data integrity principles is advantageous.
  • Strong technical aptitude, willingness to learn equipment operations, and ability to perform basic process troubleshooting.
  • Ability to work hands-on in a cleanroom, including prolonged standing, equipment movement, and manual handling of items up to 12 kg.
  • Willingness to work a rotating 12-hour shift pattern and maintain required training and operational competencies.

Culture & Benefits

  • Agile career development and ongoing learning opportunities.
  • Inclusive and ethical working environment focused on collaboration, accountability, excellence, passion, and integrity.
  • Performance-based compensation programs and shift allowances.
  • Daily company bus service from MRT locations across Singapore to the Tuas site.
  • Fully paid medical insurance, with partially subsidized family-member coverage available.

Π‘ΡƒΠ΄ΡŒΡ‚Π΅ остороТны: Ссли Ρ€Π°Π±ΠΎΡ‚ΠΎΠ΄Π°Ρ‚Π΅Π»ΡŒ просит Π²ΠΎΠΉΡ‚ΠΈ Π² ΠΈΡ… систСму, ΠΈΡΠΏΠΎΠ»ΡŒΠ·ΡƒΡ iCloud/Google, ΠΏΡ€ΠΈΡΠ»Π°Ρ‚ΡŒ ΠΊΠΎΠ΄/ΠΏΠ°Ρ€ΠΎΠ»ΡŒ, Π·Π°ΠΏΡƒΡΡ‚ΠΈΡ‚ΡŒ ΠΊΠΎΠ΄/ПО, Π½Π΅ Π΄Π΅Π»Π°ΠΉΡ‚Π΅ этого - это мошСнники. ΠžΠ±ΡΠ·Π°Ρ‚Π΅Π»ΡŒΠ½ΠΎ ΠΆΠΌΠΈΡ‚Π΅ "ΠŸΠΎΠΆΠ°Π»ΠΎΠ²Π°Ρ‚ΡŒΡΡ" ΠΈΠ»ΠΈ ΠΏΠΈΡˆΠΈΡ‚Π΅ Π² ΠΏΠΎΠ΄Π΄Π΅Ρ€ΠΆΠΊΡƒ. ΠŸΠΎΠ΄Ρ€ΠΎΠ±Π½Π΅Π΅ Π² Π³Π°ΠΉΠ΄Π΅ β†’