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6 часов назад

Senior Process Engineer (Pharmaceutical Manufacturing)

101 184 - 158 100CAD
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
Senior Process Engineer (Pharmaceutical Manufacturing): Developing and optimizing GMP-regulated pharmaceutical manufacturing processes for clinical-to-commercial production with an accent on technology transfer, process scale-up, equipment design, and quality control strategies. Focus on identifying and mitigating process risks, qualifying critical process parameters, commissioning equipment, and improving operational efficiency.

Location: Windsor, Nova Scotia, Canada

Salary: CAD 101,184–158,100 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 clinical-to-commercial production, including microbial fermentation, synthetic small molecules, plasmid DNA, mRNA, LNP, and sterile filling.

What you will do

  • Lead process engineering analyses for technology transfers, including cycle time, equipment fit, required technologies, and scale-up strategy.
  • Partner with cross-functional teams and clients to evaluate technical feasibility and develop robust commercial processes.
  • Identify, scale, and qualify critical process parameters, critical quality attributes, critical aspects, and control strategies.
  • Develop process flow diagrams, mass balances, conceptual design packages, and return-on-investment reports.
  • Design, procure, start up, commission, and troubleshoot pharmaceutical process equipment and instrumentation.
  • Participate in P&ID, HAZOP, design, project, gap analysis, and departmental quality programming activities.

Requirements

  • Bachelor’s or master’s degree or equivalent.
  • 8+ years of relevant experience in a GMP-regulated environment.
  • Postgraduate credentials, certification, or licensing may be required.
  • Ability to prioritize project deliverables and manage budgets, schedules, process risks, and technical documentation.
  • Ability to work with cross-functional departments and clients on process engineering and manufacturing projects.

Culture & Benefits

  • Full-time daytime schedule with no defined end date.
  • Eligibility for bonus, stock, and benefits.
  • Approximately 10% travel required.
  • Work in advanced manufacturing focused on improving therapeutic production and patient care.

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