Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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В Company hidden четко описана руководящая роль в производстве вакцин с широкими задачами по GMP и улучшению процессов, но контракт всего на восемь месяцев не дает долгосрочной определенности.
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Контракт на 8 месяцевЧеткая зона ответственностиПроизводство вакцин
Оценка от Hirify AI
Мэтч & Сопровод
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Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Technical Group Leader (Pharmaceutical Manufacturing): Leading technical staff and coordinating influenza drug-substance manufacturing activities in a GMP-regulated B200 upstream operation with an accent on production scheduling, documentation accuracy, equipment readiness, and data management. Focus on leading deviations and investigations, validating equipment, maintaining SAP and process data, and coordinating process-improvement projects.
Location: Toronto, Ontario, Canada; onsite. Work schedule: Friday to Tuesday, 06:00–14:00, subject to change.
Pay rate: $56.02 per hour.
Company
hirify.global is an R&D-driven, AI-powered biopharmaceutical company developing medicines and vaccines, including more than 500 million vaccine doses annually.
What you will do
Schedule and coordinate technical staff supporting influenza manufacturing activities in the B200 upstream area.
Review GMP documentation, maintain equipment readiness, coordinate materials and supplies, and supervise material handling.
Coordinate SAP transactions, process orders, master recipes, inventory, work orders, investigations, deviations, and other manufacturing data.
Perform and delegate cleaning checks, production calculations, utility sampling, environmental monitoring, maintenance, and troubleshooting.
Train staff on GMP, SOP, HSE, PPE, problem-solving, and safe working practices while maintaining inspection readiness.
Coordinate facility, equipment, validation, and process-improvement projects; prepare specifications, protocols, reports, SOPs, BPRs, CCRs, and CAPAs.
Requirements
Minimum three-year college diploma in Biochemistry, Microbiology, Bioengineering, Biotechnology, Chemistry, Chemical Engineering, Pharmaceutical Sciences, or a related Life Sciences field.
Minimum three years of relevant work experience or equivalent.
Proficiency in pharmaceutical manufacturing, protein purification, centrifugation, tangential flow filtration, and cGMP is preferred.
Experience with automated and manually operated process equipment.
Strong understanding of computerized systems, data management systems, quality management systems, SAP, SOPs, automation, and relevant software applications.
Nice to have
Bachelor’s degree in Biochemistry, Microbiology, Bioengineering, Biotechnology, Chemistry, Chemical Engineering, Pharmaceutical Sciences, or a related Life Sciences field, with a minimum of three years of relevant work experience.
Culture & Benefits
Fixed-term contract for eight months.
Work alongside a supportive, future-focused team in a global healthcare organization.
Opportunities for talent development, promotion, lateral moves, and international career growth.
Rewards package recognizing contributions and impact.
Equal-opportunity workplace with recruitment accommodations available for persons with disabilities upon request.
Hiring process
Complete the Workday application form and attach a resume when submitting the application; applications without both items will not be considered.
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