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Supervisor, Production (Pharmaceutical Manufacturing)

80 000 - 100 000$
Формат работы
onsite
Тип работы
fulltime
Грейд
lead
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
Supervisor, Production (Pharmaceutical Manufacturing): Supervising liquid pharmaceutical production personnel and processes during a 12-hour overnight shift with an accent on aseptic and terminally sterilized filling, capping, lyophilization, and cGMP compliance. Focus on coordinating production schedules, investigating deviations, implementing corrective actions, developing staff, and supporting product release through batch-record review.

Location: Melrose Park, Illinois, United States; onsite, 12-hour overnight shift

Salary: $80,000–$100,000 annually, plus a $153.85 bi-weekly overnight shift differential and a bonus target of 6% of base salary.

Company

hirify.global develops and manufactures products for healthcare and pharmaceutical applications.

What you will do

  • Supervise and coordinate liquid production personnel and processes across an assigned production area.
  • Coordinate daily and weekly production schedules, including component preparation, aseptic and terminally sterilized filling, capping, and lyophilization.
  • Work on the production floor with management and support functions to maintain operational continuity across shifts.
  • Lead deviation investigations, perform root cause analysis, and implement corrective and preventive actions.
  • Coordinate staffing, training, performance evaluation, and continuous process improvement activities.
  • Review production batch records, support product release, maintain SOPs, and provide production data for efficiency reporting.

Requirements

  • Bachelor’s degree and/or relevant work experience.
  • At least five years of experience in a production or manufacturing environment.
  • At least two years of experience in a leadership role.
  • Ability to work assigned shifts and provide coverage for vacations and staffing gaps.
  • English proficiency required: ability to speak, read, write, and understand English for regulated workplace communications.
  • Ability to comply with company policies, safety programs, quality systems, and cGMP requirements.

Nice to have

  • Experience in an FDA-regulated industry.

Culture & Benefits

  • Medical, prescription drug, dental, and vision coverage.
  • 401(k) plan with company contributions.
  • Paid vacation, holidays, and personal days.
  • Life insurance, disability coverage, employee assistance program, and wellness program.
  • Employment is at-will and subject to applicable federal and state laws.

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