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9 часов назад

Supervisor, Manufacturing - DAP (Night Shift) (Biomanufacturing)

75 000 - 112 500$
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, Manufacturing - DAP (Night Shift) (Biomanufacturing): Leading shift-level execution of a DAP manufacturing line, coordinating technicians, equipment, materials, production schedules, quality, cost, and safety with an accent on cGMP compliance, process execution, and cross-functional operations. Focus on resolving process problems, improving manufacturing performance, managing deviations and corrective actions, and developing the technician team across a rotating 12-hour night shift.

Location: USA - OH - West Chester; onsite night shift, 6:00 PM–6:30 AM, on a rotating 2-on/2-off, 3-on/3-off schedule

Salary: $75,000–$112,500 per year

Company

hirify.global is a technology-focused biomanufacturing company developing sustainable, high-tech, end-to-end manufacturing solutions for medicines.

What you will do

  • Lead technicians and direct equipment, materials, staffing, and schedules to meet production, quality, safety, and cost targets.
  • Execute process confirmations and ensure DAP line operations follow approved procedures and standards.
  • Partner with MSAT, Engineering, and Quality to resolve process issues and optimize operational performance.
  • Drive continuous improvement through team-based problem solving, KPIs, lean behaviors, and cross-shift collaboration.
  • Support the design, qualification, lifecycle management, and capital planning of manufacturing equipment, facilities, and processes.
  • Manage employee relations, hiring, performance management, training, qualification, and career development for direct reports.

Requirements

  • Basic knowledge of packaging or manufacturing operations in a pharmaceutical, biotechnology, or other cGMP-regulated environment.
  • Strong leadership, communication, writing, independent judgment, and team development skills.
  • Ability to work with cross-functional teams on initiatives affecting DAP operations.
  • Basic knowledge of Microsoft Office and computer applications.
  • Preferred: bachelor’s degree in engineering, science, or business; 5+ years of pharmaceutical, biotechnology, or cGMP manufacturing experience with supervisory or leadership experience.
  • Work authorization or visa sponsorship is not available for this position.

Nice to have

  • Experience in lean manufacturing, formulation, filling, packaging, validation, technology transfer, or change control.
  • Strong mechanical, electrical, troubleshooting, and problem-solving abilities.
  • Experience managing technical programs or projects.
  • Basic knowledge of generative AI language tools such as Claude.

Culture & Benefits

  • Annual cash bonus program and 401(k) plan with company match.
  • Medical, dental, vision, life, and disability insurance.
  • Paid vacation, holidays, and other paid leaves of absence.
  • Tuition reimbursement, family-building benefits, and caregiving support.
  • Work requires adherence to cGMP, quality management, EHS, safety, and regulatory standards, including use of protective equipment.

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