6 часов назад
Technical Group Leader (Pharmaceutical Manufacturing)
54 - 52CAD
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Technical Group Leader (Pharmaceutical Manufacturing): Leading influenza manufacturing operations and technical staff in a GMP-regulated B200 upstream facility with an accent on production coordination, computerized manufacturing data, equipment maintenance, and quality compliance. Focus on coordinating investigations and CAPA/CCR activities, supporting equipment qualification, maintaining process orders and recipes, and ensuring inspection readiness.
Location: Toronto, Ontario, Canada; onsite. Monday–Friday, 2:00 pm–10:00 pm.
Pay rate: $54.52 per hour.
Company
is an R&D-driven, AI-powered biopharmaceutical company developing medicines and vaccines, including influenza manufacturing operations.
What you will do
- Schedule and coordinate daily and weekly work for technical staff supporting B200 influenza manufacturing operations.
- Review GMP records, SOPs, logbooks, batch production records, monitoring charts, and electronic documentation for accuracy and completion.
- Coordinate SAP transactions, capacity planning, material and personnel scheduling, work orders, master recipes, process orders, inventory, and manufacturing data.
- Support equipment maintenance, validation, calibration, cleaning, utility sampling, environmental monitoring, and inspection readiness.
- Lead deviations and investigations, and manage change controls and CAPA activities through completion.
- Coordinate production and process improvement projects with Manufacturing Technology, Engineering, Maintenance, Automation, Quality Operations, and laboratory teams.
Requirements
- Minimum three-year college diploma in biochemistry, microbiology, bioengineering, biotechnology, chemistry, chemical engineering, pharmaceutical sciences, or a related life sciences field.
- At least three years of relevant work experience or equivalent; a bachelor’s degree in a related field is preferred.
- Experience in pharmaceutical manufacturing, protein purification, centrifugation, tangential flow filtration, and cGMP practices 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 related applications.
- Ability to work onsite in Toronto and during the stated Monday–Friday afternoon/evening schedule.
Culture & Benefits
- Work alongside a supportive, future-focused team advancing medicines and vaccines.
- Opportunities for professional growth through promotion or lateral career moves, including international opportunities.
- Rewards package recognizing employee contribution.
- provides equal employment opportunities and recruitment accommodations for persons with disabilities upon request.
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