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Engineer, Packaging (Pharmaceutical Manufacturing)

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
Engineer, Packaging (Pharmaceutical Manufacturing): Designing, validating, and optimizing primary packaging systems for GMP drug products with an accent on packaging materials, aseptic systems, sterilization, and product quality. Focus on supporting process validation, stability and shipping studies, technology transfers, investigations, CAPAs, and GMP manufacturing equipment qualification.

Location: US - Tampa, FL; fully site-based role

Company

hirify.global operates globally connected manufacturing sites focused on producing medicines and turning life-science innovations into viable therapies.

What you will do

  • Lead the design, selection, and optimization of primary packaging materials, components, and systems for GMP drug products.
  • Collaborate with Manufacturing, Quality Assurance, Supply Chain Operations, MSAT, and other stakeholders on compliant and efficient packaging solutions.
  • Provide technical expertise across vials, bottles, flexible bags, aseptic form/fill/seal systems, sterilization, labels, and single-use technologies.
  • Plan and support process validation, stability studies, product interaction assessments, and shipping studies.
  • Drive packaging performance, operational efficiency, lean improvement, innovation, and GMP compliance initiatives.
  • Support technology transfers, change controls, deviations, investigations, CAPAs, manufacturing documentation, batch record review, and equipment qualification.

Requirements

  • Bachelor’s degree in Science, Engineering, or a related technical field.
  • At least 5 years of experience in a pharmaceutical cGMP environment.
  • Expertise in primary packaging design, material selection, packaging components, and packaging systems.
  • Experience with packaging technologies, process validation, stability studies, product interaction assessments, and shipping studies.
  • Experience supporting GMP manufacturing operations, technology transfers, deviations, investigations, CAPAs, change controls, and continuous improvement.
  • Strong technical documentation skills, including Master Batch Records and qualification protocols, with effective cross-functional collaboration.

Culture & Benefits

  • Agile career development and a dynamic working culture.
  • Inclusive and ethical workplace.
  • Performance-focused compensation programs.
  • Medical, dental, and vision insurance.
  • In-person collaboration in a GMP manufacturing environment.

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