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5 часов назад

Sr Engineer (Packaging)

115 495 - 156 257$
Формат работы
onsite
Тип работы
fulltime
Грейд
senior
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
Sr Engineer (Packaging): Developing, implementing, maintaining, and improving pharmaceutical packaging platforms, configurations, components, materials, and processes with an accent on technology transfers, qualification activities, lifecycle management, and cGMP compliance. Focus on solving moderately complex engineering problems, identifying technical risks, coordinating cross-functional delivery, and implementing scalable packaging improvements.

Location: Thousand Oaks, California, United States

Salary: USD 115,494.60–156,257.40 annually

Company

hirify.global is a biotechnology company that researches, manufactures, and delivers medicines for serious illnesses across oncology, inflammation, general medicine, and rare disease.

What you will do

  • Own technical deliverables for packaging projects, components, systems, and platform areas while ensuring quality, reliability, and compliance.
  • Develop, implement, maintain, and improve packaging platforms, configurations, equipment, processes, and lifecycle management programs.
  • Evaluate, qualify, and sustain packaging components, materials, processes, and platform elements for pharmaceutical products.
  • Lead or support technical assessments, test protocols, qualification activities, engineering reports, specifications, procedures, and change controls.
  • Support technology transfers, new product introductions, and site-to-site or clinical-to-commercial packaging transitions.
  • Collaborate with Product Development, Operations, Manufacturing, Quality, Regulatory, Supply Chain, and other functions to deliver scalable packaging solutions.

Requirements

  • Doctorate degree; or a master’s degree with 2 years of engineering experience; or a bachelor’s degree with 4 years of engineering experience; or equivalent experience with an associate’s degree or high school diploma/GED.
  • Experience in packaging, manufacturing, process, product development, device or combination product development, clinical supply, or regulated technical operations.
  • Knowledge of cGMP expectations, change control, qualification, validation, technical writing, and regulated manufacturing environments.
  • Ability to own technical deliverables, identify and resolve risks, communicate progress and issues, and work effectively with cross-functional partners.
  • Strong project management, communication, collaboration, technical writing, and technical problem-solving skills.

Culture & Benefits

  • Collaborative, innovative, and science-based work environment.
  • Health, dental, and vision coverage, life and disability insurance, and flexible spending accounts.
  • Retirement and savings plan with company contributions and stock-based long-term incentives.
  • Discretionary annual bonus program and award-winning time-off plans.
  • Career development opportunities and flexible work models where applicable.

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