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3 дня назад

Sr Engineer (Packaging Engineering)

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 Engineering): Developing, implementing, and improving pharmaceutical packaging platforms, configurations, processes, and lifecycle activities with an accent on technical qualification, regulated operations, and technology transfers. Focus on solving moderately complex packaging and manufacturing problems, managing technical risks, and delivering compliant solutions across cross-functional teams.

Location: Thousand Oaks, California, United States

Company

Amgen develops, manufactures, and delivers biotechnology 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.
  • Develop, implement, maintain, and improve pharmaceutical packaging platforms, configurations, equipment, and processes.
  • Evaluate, qualify, and sustain packaging components, materials, processes, and platform elements.
  • Lead or support technical assessments, test protocols, qualification activities, engineering reports, specifications, procedures, and change controls.
  • Support technology transfers, new product introductions, site start-ups, and packaging lifecycle management.
  • Partner with Product Development, Operations, Manufacturing, Quality, Regulatory, Supply Chain, and other functions to deliver compliant and 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; or an associate degree with 8 years; or a high school diploma/GED with 10 years of engineering experience.
  • Experience in packaging, manufacturing, process, product development, device, combination product, 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 technical progress, and collaborate cross-functionally.
  • Strong project management, communication, collaboration, technical writing, and technical problem-solving skills.

Nice to have

  • Experience with automated equipment implementation, platform standardization, site start-ups, or process improvements.
  • Experience developing or improving clinical or commercial packaging configurations and lifecycle management programs.

Culture & Benefits

  • Collaborative, innovative, and science-based work environment.
  • Health, dental, vision, life, disability, and flexible spending benefits for eligible employees and dependents.
  • Retirement and savings plan with company contributions, stock-based long-term incentives, and a discretionary annual bonus program.
  • Award-winning time-off plans and career development opportunities.
  • Flexible work models may be available where applicable to the role.

Hiring process

  • Applications are accepted until a candidate is selected or a sufficient number of applications is received.
  • Visa sponsorship is not guaranteed.

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