team leadershipbiotechnologyquality systemscontinuous improvementcgmpmanufacturing operationsgmp compliancebiologics manufacturing
Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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Company hidden предлагает понятную руководящую роль в производстве биопрепаратов и возможности для развития, но смены по 12 часов с чередованием графика и неуказанная зарплата затрудняют оценку условий.
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Зарплата не указанаСменный графикПонятные обязанностиОпыт в биотехеРост и развитие
Оценка от Hirify AI
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Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Manufacturing Supervisor (Biotechnology): Leading on-site production of therapeutic proteins in a regulated cGMP environment with an accent on safety, compliance, production scheduling, and team development. Focus on reviewing batch records, coordinating cross-functional troubleshooting, driving continuous improvement, and maintaining inspection readiness.
Location: On-site in Portsmouth, New Hampshire, United States. Rotating 12-hour day shifts from 7:00 AM to 7:00 PM on an alternating 2-2-3 schedule.
Company
hirify.global operates more than 30 sites across five continents and manufactures medicines and therapeutic products for life sciences customers.
What you will do
Lead daily manufacturing operations for safe, compliant, and on-time execution of production schedules.
Coach, train, and develop operators through performance management, career planning, and ongoing development.
Monitor production activities for compliance with cGMP requirements, quality systems, SOPs, and safety standards.
Review batch records, logbooks, and production documentation to support timely batch release with minimal errors.
Coordinate with Manufacturing, Engineering, MSAT, Scheduling, and other functions to troubleshoot equipment and process issues.
Support recruiting, onboarding, staffing, workforce planning, continuous improvement, and inspection readiness.
Requirements
Associate’s or bachelor’s degree in a science-related discipline, or a high school diploma or equivalent with relevant experience.
Experience in manufacturing within a cGMP-regulated environment.
Previous supervisory or team leadership experience is preferred.
Strong understanding of quality systems, GMP compliance, and manufacturing operations.
Experience leading employees through training, coaching, and performance development.
Strong communication, problem-solving, decision-making, organizational, and cross-functional collaboration skills.
Culture & Benefits
Agile career environment with opportunities for leadership development and career growth.
Exposure to advanced biologics manufacturing processes and technologies.
Collaborative work with cross-functional partners across the site.
Medical, dental, and vision insurance.
Compensation programs recognizing high performance.
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