9 часов назад
Supervisor, Manufacturing - DAP (Night Shift) (Biomanufacturing)
75 000 - 112 500$
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
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
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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