4 дня назад
Principal Manufacturing Innovation Strategist (Biopharma Manufacturing)
121 644 - 190 069CAD
Мэтч & Сопровод
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Описание вакансии
Текст:
TL;DR
Principal Manufacturing Innovation Strategist (Biopharma Manufacturing): Shaping manufacturing strategy and developing capital projects for GMP production of biologics and small-molecule APIs with an accent on process systems, technology transfer, automation, quality, and lifecycle management. Focus on leading complex capital projects, building three- to five-year manufacturing plans, evaluating technologies and partnerships, and solving enterprise-level engineering challenges.
Location: Charlottetown, Prince Edward Island, Canada; remote work is available.
Salary: CAD 121,644–190,069 per year, plus bonus eligibility, stock, and benefits.
Company
BIOVECTRA, part of , provides contract development and manufacturing services for active pharmaceutical ingredients and advanced pharmaceutical products, including biologics, small molecules, plasmid DNA, mRNA, LNP, and sterile filling.
What you will do
- Provide technical leadership, coaching, and mentorship to engineering and project teams.
- Guide process scale-up, technology transfer, facility modifications, and lifecycle optimization.
- Develop three- to five-year manufacturing and capital plans with Finance and corporate leadership.
- Evaluate facility expansions, acquisitions, outsourced manufacturing, technology transfers, and strategic partnerships.
- Lead major capital projects from concept through commissioning and qualification within approved scope, schedule, budget, risk, and value targets.
- Advise executives on manufacturing technologies, risks, opportunities, business cases, and enterprise-level engineering initiatives.
Requirements
- Bachelor’s degree in engineering, biotechnology, biopharmaceutical sciences, chemistry, or a comparable discipline.
- At least 10 years of experience in pharmaceutical manufacturing, with substantial biologics and/or API experience.
- Experience leading complex capital projects and strategic initiatives.
- Thorough knowledge of GMP, Annex 1, ICH guidance, and regulatory expectations from the FDA, EMA, and Health Canada.
- Availability for approximately 10% travel and a regular day shift.
Nice to have
- Master’s degree and/or MBA.
- Professional Engineer designation or equivalent credential.
- Expertise in biologics production and small-molecule API production.
Culture & Benefits
- Full-time employment with no specified end date.
- Option to work remotely.
- Eligibility for bonus, stock, and benefits.
- Work focused on improving compliance, quality, capacity, reliability, cost, and long-term manufacturing performance.
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