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5 дней назад

Engineer II - Frontline Engineering (Downstream Operations) (Biotech)

93 000 - 155 000$
Формат работы
onsite
Тип работы
fulltime
Грейд
middle
Английский
b2
Страна
US
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
Engineer II - Frontline Engineering (Downstream Operations) (Biotech): Supporting 24/7 downstream biopharmaceutical manufacturing as a system and equipment subject matter expert with an accent on GMP readiness, equipment reliability, and operational improvement. Focus on investigating complex unplanned events, leading improvement projects, qualifying new systems, and supporting CAPEX projects and new product transfers.

Location: Vacaville, California, United States; fully site-based

Salary: $93,000–$155,000 annual base salary, plus a performance-related bonus.

Company

hirify.global operates more than 30 sites across five continents to support the development and manufacture of biopharmaceutical medicines.

What you will do

  • Support 24/7 manufacturing operations as the subject matter expert for systems and equipment, ensuring readiness and fitness for purpose.
  • Investigate complex unplanned events using structured problem solving and root cause analysis.
  • Lead small to medium-sized improvement projects focused on operational excellence and reliability.
  • Collaborate with Manufacturing, Quality Assurance, Engineering, Maintenance, MSAT, Automation, and EHS to meet production schedules.
  • Support startup, commissioning, qualification, CAPEX projects, and new product transfers from design through qualification.
  • Analyze equipment and process data to identify trends and implement improvements.

Requirements

  • Bachelor’s degree in Chemical Engineering or a related field.
  • Strong experience with pharmaceutical or biotech manufacturing equipment and systems in a GMP-regulated environment.
  • Hands-on experience in downstream biopharmaceutical manufacturing at a commercial GMP facility.
  • Experience with chromatography, viral filtration, ultrafiltration/diafiltration, or bulk drug substance operations.
  • Project leadership experience delivering improvements and system changes, along with strong communication and collaboration skills.
  • Proficiency with SAP, MS Office, P&IDs, and data visualization tools is preferred.

Culture & Benefits

  • Work closely with cross-functional teams in person in a GMP-regulated manufacturing environment.
  • Medical, dental, and vision insurance.
  • 401(k) matching plan.
  • Life insurance and short-term and long-term disability insurance.
  • Employee assistance programs and paid time off.

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