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17 часов назад

Manufacturing Engineer (Pharmaceutical Manufacturing)

82 882 - 129 503CAD
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
Canada
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
Manufacturing Engineer (Pharmaceutical Manufacturing): Designing, procuring, installing, commissioning, and qualifying pharmaceutical processes and equipment with an accent on regulated manufacturing, equipment validation, and project delivery. Focus on starting up process equipment, developing qualification protocols, updating AutoCAD drawings, troubleshooting instrumentation, and coordinating engineering, manufacturing, maintenance, vendors, and contractors.

Location: Windsor, Nova Scotia, Canada

Salary: CAD 82,882–129,503 per year, plus eligibility for bonus, stock, and benefits

Company

hirify.global's BIOVECTRA business develops and manufactures active pharmaceutical ingredients and advanced therapeutics for pharmaceutical and biotechnology clients.

What you will do

  • Design, procure, install, commission, and qualify pharmaceutical processes, manufacturing systems, equipment, and instrumentation.
  • Prioritize project deliverables and coordinate startup, commissioning, validation, and qualification activities with internal and external groups.
  • Develop equipment qualification protocols, execute testing, collect data, and perform statistical analysis.
  • Prepare and review Turn Over Packages, update AutoCAD and as-built drawings, and organize project documentation.
  • Troubleshoot equipment and instrumentation, support maintenance with repairs and calibration, and recommend replacement parts.
  • Collaborate with tradespeople, vendors, engineering, manufacturing, maintenance, and clients while participating in P&D, HAZOP, PHA, and design reviews.

Requirements

  • Bachelor of Science in Engineering, preferably Mechanical or Chemical Engineering.
  • 5+ years of experience in pharmaceutical manufacturing or a similar regulated environment.
  • Hands-on experience starting up and commissioning instruments and process equipment.
  • Understanding of fire and building codes, GxP, ISO, ICH, OHS, CSA, NFPA, CEPA, and other applicable regulatory standards.
  • Strong written and verbal communication, financial awareness, and ability to work independently and under pressure.
  • Excellent computer skills, including Excel, Word, MS Project, and AutoCAD.

Nice to have

  • Six Sigma or Lean certification.
  • PMP certification.
  • Red Seal trade or CET designation.
  • Project management experience.

Culture & Benefits

  • Full-time weekly schedule with day-shift work.
  • Eligibility for bonus, stock, and benefits.
  • Occasional travel may be required.
  • Opportunity to work with advanced manufacturing technologies and contribute to improved therapeutics.

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