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3 часа назад

Production Operator I (Pharmaceutical)

Формат работы
onsite
Тип работы
fulltime
Грейд
junior
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

Production Operator I (Pharmaceutical): Executing cGMP pharmaceutical manufacturing activities including equipment operation, batch processing, and documentation with an accent on safety, quality, and right-first-time performance. Focus on operating specialized machinery like tablet presses and fluid bed dryers while maintaining strict cleanroom standards and regulatory compliance.

Location: On-site in Middletown, DE

Company

hirify.global is a global provider of R&D and manufacturing services for the pharmaceutical, biotech, and medical device industries.

What you will do

  • Perform manufacturing steps such as dispensing, mixing, and packaging according to approved batch records.
  • Set up, operate, and monitor pharmaceutical equipment including blenders, tablet presses, and encapsulators.
  • Conduct in-process checks and document results to ensure data integrity and quality standards.
  • Execute line clearances and equipment changeovers to minimize production downtime.
  • Work in classified ISO 8–7 cleanroom environments following aseptic techniques.
  • Collaborate with cross-functional teams including QA, QC, and Facilities to support investigations and process improvements.

Requirements

  • Must be able to work on-site in Middletown, DE.
  • Experience working with pharmaceutical manufacturing equipment such as tablet presses, encapsulators, or fluid bed dryers.
  • Fundamental understanding of cGMPs, cleanroom behaviors, and data-integrity expectations.
  • Ability to stand for extended periods and lift up to 50 lbs.
  • Bachelor’s degree or technical certificate in a science or technical field preferred.
  • Minimum of 3 years of experience in a regulated industrial setting like GMP manufacturing, food/beverage, or biotech.

Culture & Benefits

  • Opportunity to work in a fast-paced, highly regulated pharmaceutical environment.
  • Involvement in continuous improvement initiatives like lean and 5S.
  • Commitment to safety and quality standards in a professional manufacturing setting.
  • Equal Opportunity Employer with a focus on inclusive hiring practices.

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