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6 дней назад

Specialist, Manufacturing (12-month fixed term contract)

24 - 35CAD
Формат работы
onsite
Тип работы
project
Грейд
middle
Английский
b2
Страна
Canada
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Мэтч & Сопровод

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Описание вакансии

Текст:
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TL;DR
Specialist, Manufacturing (12-month fixed term contract) (Biomanufacturing): Operating upstream and downstream biopharmaceutical manufacturing equipment in a cGMP environment with an accent on aseptic processing, filtration, chromatography, and batch documentation. Focus on executing CIP/SIP procedures, operating bioreactors and UF/DF/TFF systems, maintaining data integrity, and supporting continuous improvement and safety initiatives.

Location: Mississauga, Ontario, Canada — onsite manufacturing facility

Base pay: CAD 24.00–34.50 per hour

Company

hirify.global is a technology-focused biomanufacturing company developing sustainable, end-to-end manufacturing solutions for biopharmaceutical production.

What you will do

  • Operate bioreactors, centrifuges, biosafety cabinets, chromatography skids, UF/DF and TFF systems, nanofiltration equipment, and other manufacturing systems.
  • Perform upstream and downstream processing, filtration, aseptic operations, in-process sampling, and basic analytical testing.
  • Execute CIP/SIP procedures and operate HMIs and computerized production systems.
  • Follow SOPs, WINs, cGMPs, safety standards, and data integrity requirements while maintaining accurate production records.
  • Identify and escalate material defects, process deviations, equipment issues, and documentation problems.
  • Support cross-training, required certifications, continuous improvement, housekeeping, and site safety initiatives.

Requirements

  • Understanding of cGMP documentation, data integrity principles, and regulated manufacturing procedures.
  • Ability to operate bioprocessing equipment and perform CIP/SIP, filtration, and materials receipt/FIFO activities according to approved procedures.
  • Bachelor’s degree or technical diploma in biochemistry, biotechnology, biology, chemistry, chemical engineering, pharmaceutical sciences, or a related discipline is preferred.
  • Two or more years of experience in biopharmaceutical, pharmaceutical, or CDMO manufacturing is preferred.
  • Experience with chromatography systems, UF/DF/TFF, nanofiltration, and bioreactors is preferred.
  • Ability to work rotating 8-hour or 12-hour shifts, including day, afternoon, and night shifts, as well as extended hours, evenings, and weekends.

Culture & Benefits

  • Work in a cGMP cleanroom environment with required gowning and PPE, including a fitted respirator.
  • Physical work includes extended standing, lifting up to 20 kg, pushing buffer drums or totes, and cleaning production suites.
  • Benefits include healthcare, dental, vision, life, long-term disability, and accidental death and dismemberment coverage.
  • Additional benefits include an annual cash bonus, RRSP/DPSP company matching, paid vacation and holidays, parental leave top-up, fertility and family-forming support, tuition reimbursement, and an employee referral program.
  • Accessibility accommodations are available throughout the recruitment process.

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