2 дня назад
Production Planning Admin (Manufacturing)
20 - 35CAD
Мэтч & Сопровод
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Описание вакансии
Текст:
TL;DR
Production Planning Admin (Manufacturing): Coordinating production activities and material usage planning for GMP-regulated manufacturing sites with an accent on master production scheduling, capacity planning, material availability, and inventory optimization. Focus on converting demand forecasts into executable plans, managing production risks and recovery schedules, and aligning manufacturing, supply chain, procurement, quality, and project management stakeholders.
Location: Windsor, Nova Scotia, Canada
Salary: CAD $20.37–$35.65 per hour, plus eligibility for bonus, stock, and benefits.
Company
, through BIOVECTRA, develops and manufactures active pharmaceutical ingredients and advanced therapeutics for clinical-to-commercial production.
What you will do
- Develop and maintain the site Master Production Schedule and support the Master Capacity Schedule.
- Convert demand forecasts into executable manufacturing plans aligned with capacity, materials, equipment, and workforce availability.
- Lead schedule reviews and planning meetings, monitor schedule adherence, and coordinate recovery plans.
- Identify and communicate production and supply risks while supporting inventory optimization and customer service levels.
- Coordinate with Manufacturing, Supply Chain, Procurement, Technical Operations, Quality, and Project Management.
- Prepare planning metrics and management reports.
Requirements
- 2+ years of experience in production planning, scheduling, or supply chain.
- Bachelor’s degree in business, science, supply chain, or a related field preferred; equivalent technical training or experience may be considered.
- Experience with ERP/MRP systems such as SAP, Oracle, SYSPRO, JDE, or Dynamics.
- Knowledge of Master Production Scheduling, Material Requirements Planning, capacity planning, inventory management, demand forecasting, and production order management.
- Understanding of GMP manufacturing operations, batch scheduling, campaign planning, change control, deviations, and quality impacts on schedule execution.
- Strong analytical, communication, organization, prioritization, and stakeholder management skills.
Nice to have
- Experience in GMP-regulated biopharmaceutical, pharmaceutical, medical device, or similar manufacturing.
- APICS/ASCM CPIM or CSCP certification.
- PMP certification or Lean Six Sigma Green Belt or higher.
Culture & Benefits
- Full-time daytime schedule with occasional travel.
- Eligibility for bonus, stock, and benefits.
- Work within an advanced manufacturing organization focused on operational excellence and therapeutic production.
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