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60 минут назад

Manufacturing Supervisor I (Pharmaceutical Manufacturing)

75 000 - 142 500$
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
Manufacturing Supervisor I (Pharmaceutical Manufacturing) (cGMP/SAP): Leading safe, compliant second-shift pharmaceutical manufacturing operations and coordinating teams to meet production schedules with an accent on safety, quality systems, regulatory compliance, and workforce development. Focus on optimizing cycle and change-over times, resolving compliance issues, managing hazardous and non-hazardous waste, and driving operational excellence improvements.

Location: Onsite in North Chicago, Illinois, United States. A2 shift: Monday–Friday, 2:30 PM–11:00 PM.

Salary: $75,000–$142,500 per year, plus benefits and eligibility for short-term incentive programs.

Company

Develops innovative medicines and healthcare solutions across immunology, oncology, neuroscience, and aesthetics.

What you will do

  • Lead safe manufacturing operations in accordance with EHS, quality, regulatory, and operational requirements.
  • Deploy and develop team members, delegate work, conduct one-to-ones and performance reviews, and maintain development plans.
  • Coordinate shift activities and handovers to meet production schedules and ensure safe execution.
  • Perform material, line-clearance, and spot checks and manage compliance issues that may affect lot completion.
  • Manage cycle times and change-over times while identifying opportunities for improvement.
  • Participate in operational excellence initiatives and manage hazardous and non-hazardous waste in accordance with procedures and regulations.

Requirements

  • Bachelor’s degree required; a degree in science or engineering is strongly preferred.
  • At least two years of manufacturing or related experience required; supervisory experience preferred.
  • Pharmaceutical industry experience is strongly preferred.
  • Proficiency with Microsoft Office and manufacturing systems such as SAP.
  • Working knowledge of safety, quality systems, and cGMPs, with experience documenting work in a highly regulated environment.
  • Good writing skills and the ability to communicate effectively with team members.

Nice to have

  • Experience in an aseptic production environment.

Culture & Benefits

  • Safety is treated as the top priority, with routine safety checks and a zero-incident focus.
  • Benefits include paid vacation, holidays, sick leave, and medical, dental, and vision insurance.
  • Eligible employees can participate in a 401(k) plan.
  • The role includes opportunities for employee training, development, and progressively challenging assignments.

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