5 дней назад
Manager, Technical Operations (Pharmaceutical Manufacturing)
93 521 - 146 126CAD
Мэтч & Сопровод
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Описание вакансии
Текст:
TL;DR
Manager, Technical Operations (Pharmaceutical Manufacturing): Leading technical operations and production teams through pharmaceutical process development, technology transfer, validation, and commercialization with an accent on microbial fermentation, synthetic small molecules, APIs, and drug products. Focus on assessing technical-transfer risks, aligning Development and Operations decisions, developing process documentation, and incorporating Process Analytical Technology into manufacturing processes.
Location: Windsor, Nova Scotia, Canada
Salary: CAD 93,521–146,126 per year, plus eligibility for bonus, stock, and benefits.
Company
’s BIOVECTRA business develops and manufactures active pharmaceutical ingredients and drug products for clinical-to-commercial production, including microbial fermentation, synthetic small molecules, plasmid DNA, mRNA, LNP, and sterile filling.
What you will do
- Manage, train, and coach production staff through direct floor-level supervision.
- Provide technical direction, influence production decisions, implement corrective actions, and maintain operational alignment.
- Coordinate Development and Operations technical decisions through process performance demonstrations, engineering runs, validation runs, and commercialization.
- Support new-project evaluations with Sales and Marketing and assess technology-transfer risks.
- Develop and approve process SOPs, training documents, and technical reports.
- Support client visits and technology-transfer projects from inception through completion, including the use of Process Analytical Technology where appropriate.
Requirements
- Bachelor of Science degree, preferably in Engineering, Chemistry, or Biochemistry.
- At least 10 years of pharmaceutical experience.
- At least 1 year of leadership experience.
- Demonstrated technology-transfer experience in the biotechnology or pharmaceutical industry.
- Knowledge of manufacturing operations, supply chain, quality assurance, validation, and quality control.
- Strong organizational, interpersonal, oral, and written communication skills.
Nice to have
- Master of Science degree.
- Experience with API and drug-product manufacturing.
- Willingness to travel occasionally.
Culture & Benefits
- Full-time daytime schedule with no end date.
- Work within an advanced manufacturing organization focused on pharmaceutical innovation and improved patient care.
- Eligibility for bonus, stock, and benefits.
- Occasional travel may be required.
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