Назад
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6 дней назад

Technical Associate

24 - 40$
Формат работы
onsite
Тип работы
fulltime
Грейд
middle
Английский
b2
Страна
US
Релокация
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
Technical Associate (Solid Dose Pharmaceutical Manufacturing): Manufacturing and supporting tablet and capsule formulations for developmental, stability, and clinical supplies with an accent on cGMP compliance, equipment operation, and batch documentation. Focus on operating complex closed-transfer systems, investigating quality issues, calculating process metrics, and leading continuous improvement with Lean Manufacturing Techniques.

Location: On premise in Groton, Connecticut, United States; regular site presence, off-shift and weekend flexibility required.

Salary: $24.22–$40.36 per hour, plus potential overtime, weekend, holiday, and other pay premiums.

Company

hirify.global develops and manufactures medicines and pharmaceutical products for patients worldwide.

What you will do

  • Manufacture tablet and capsule solid dosage forms for developmental, stability, and clinical studies.
  • Set up, operate, clean, and maintain complex pharmaceutical manufacturing equipment and closed-transfer systems.
  • Prepare and execute batch records, logbooks, labels, electronic records, and in-process documentation.
  • Support equipment lifecycle documentation, SOP creation and revision, quality reviews, investigations, and corrective actions.
  • Perform operator care and maintain the cGMP manufacturing space.
  • Lead continuous improvement projects using Lean Manufacturing Techniques and collaborate with Operations, Quality, Technical Support, and GWE.

Requirements

  • High school diploma or GED.
  • At least 2 years of cGMP experience in a biotechnology manufacturing or laboratory environment.
  • Operational knowledge of computerized systems, production control systems, ERP systems, and other business applications.
  • Strong Microsoft Office skills, especially Word and Excel, with excellent oral and written communication.
  • Ability to work safely and effectively in a matrix team environment.
  • Permanent authorization to work in the United States is required; visa sponsorship is not available.

Nice to have

  • Bachelor’s degree.
  • Knowledge of pharmaceutical solid-dose formulation, novel processing equipment, or commercial processing standards.
  • Mechanical aptitude and willingness to perform hands-on manual work.

Culture & Benefits

  • Safety, quality, compliance, teamwork, and continuous improvement are central to the work.
  • Work involves standing, walking, bending, climbing, reaching, and lifting up to 55 pounds.
  • Personal protective equipment, including gloves, a Tyvek suit, and respiratory protection, may be required.
  • Benefits include a 401(k) with hirify.global contributions, retirement savings contributions, paid vacation and holidays, caregiver, parental and medical leave, and medical, prescription, dental, and vision coverage.
  • Relocation assistance may be available based on business needs and eligibility.

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