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Added 1 day ago
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Associate Director, Supply Chain Planning
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Hamilton, ON · Canada – Hamilton – Longwood Road South
- Full-time
Job Title: Associate Director, Supply Chain Planning
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AstraZeneca

Associate Director, Supply Chain Planning

Hamilton, ON, Canada
Canada – Hamilton – Longwood Road South, Canada

Full-time

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Job details

Job type: Full-time
Apply by: Oct 15, 2026
Experience: 8+ years of experience in production planning, scheduling, or supply chain experience, preferably within the pharmaceutical, biotech, or clinical research sectors.
Posting language: English
Posted: Oct 1, 2026

Original job description

Job Title: Associate Director, Supply Chain Planning

Location: Hamilton, Ontario

Onsite 5 days/week

Description:

Fusion Pharmaceuticals, part of the AstraZeneca Group, is redefining precision oncology with next‑generation radioconjugates that deliver powerful alpha‑emitting payloads directly to tumors. Our pipeline spans multiple first‑in‑class programs - backed by a GMP‑compliant, brand new radiopharmaceutical facility in Hamilton, we’re turning groundbreaking science into real‑world impact for patients. Join us at the forefront of radiopharma innovation and be part of turning breakthrough science into meaningful outcomes for patients - come build what’s next with us!

The Role:

We are seeking a strategic and analytical Associate Director of Supply Chain Planning to lead clinical supply forecast planning and drive cross-functional alignment. In this vital leadership role, you will be the linchpin for global clinical supply visibility, translating complex clinical trial protocols and enrollment forecasts into executable supply plans. You will direct the Sales and Operations Planning (S&OP) processes. You will focus on identifying risks early and serve as the main contact for supply chain health with collaborators inside and outside the company.

Responsibilities:

Host recurring Sales and Operations Planning (S&OP) meetings to align cross-functional partners.
Lead the systematic collection and consolidation of clinical trial drug demand from multiple studies, translating Phase 1–3 clinical trial protocols and enrollment forecasts into executable supply plans.
Develop and deliver high-level Demand and Supply reports, collaborate cross-functionally to define and implement long-range and short-range supply strategies.
Proactively identify and communicate supply chain risks, establishing early-warning indicators for potential bottlenecks, shortages, or timeline shifts, and driving risk mitigation strategies.
Ensure internal and external manufacturing alignment with evolving S&OP demand forecasts and scheduling requirements.
Support annual budgeting process and monitor financial forecasts.
Develop and maintain Standard Operating Procedures (SOPs) and Work Instructions for core departmental processes and supply activities to ensure GxP compliance and consistency.
Plan and oversee patient doses and overall manufacturing operations.
Participate in ongoing optimization of planning workflows, system enhancements, and change control assessments.
Perform other related operational duties as required by the business.

Qualifications:

Bachelor’s degree in Supply Chain, Engineering, Life Sciences, or Finance. A Master’s degree or MBA is highly preferred.
8+ years of experience in production planning, scheduling, or supply chain experience, preferably within the pharmaceutical, biotech, or clinical research sectors.
Expert-level capability in analyzing complex datasets, modeling supply scenarios, and presenting risk/demand forecasts to executive partners.
Strong command of ERP/MRP systems(e.g. SAP or specialized clinical supply management systems like Perceptive RTSM) and advanced data management tools (e.g. Microsoft Excel, SharePoint, and workflow automation tools).
Familiarity with GMP (Good Manufacturing Practices) and Standard Operating Procedures within a regulated manufacturing environment.
Outstanding ability to synthesize complex clinical data into clear, proactive risk communications for both technical and non-technical partners.
Able to work flexible hours to accommodate global time zones as needed.

Desirable:

Familiarity with clinical trial phases (Phase I–III), blinding/randomization concepts, and the strict timelines required for patient-specific dosing.
Proven experience in cell therapy or radiopharmaceutical supply chain operations is a plus.
Familiarity with Global clinical distribution networks, import/export regulations, and short shelf-life material logistics.
Experience leading change control assessments, deviation investigations, or CAPA (Corrective and Preventive Actions) workflows within a GxP environment.

Great People want to Work with us! Find out why:

Are you interested in working at AZ, apply today!

AstraZeneca is an equal opportunity employer that is committed to diversity and inclusion and providing a workplace that is free from discrimination. AstraZeneca is committed to accommodating persons with disabilities. Such accommodation is available on request in respect of all aspects of the recruitment, assessment and selection process and may be requested by emailing AZCHumanResources@astrazeneca.com

⠀

Annual base salary for this position ranges from 123,997.60 to 162,746.85.

AstraZeneca is committed to providing fair and equitable compensation opportunities to all colleagues. Our compensation policies and practices have been designed to allow colleagues to progress through the salary range over time as they progress in their role. The range provided in this posting represents an offer pay range used in a majority of situations. The base pay offered will vary depending on multiple individualized factors, including the candidate's skills and experience, job-related knowledge, and other specific business and organizational needs. In some cases, offers outside the range may also be considered to address unique circumstances.

In addition, our permanent positions offer an annual Variable Pay Bonus/Short Term Incentive opportunity as well as eligibility to participate in our equity-based long-term incentive program (if applicable to role). Benefits offered for permanent roles include a competitive Flex Benefits & Retirement Savings Program, 4 weeks’ paid vacation, and annual Personal Days. Fixed Term Contract/Temporary positions (excluding students) are offered a Contract Benefits Program.

We are using AI as part of the recruitment process.

This advertisement relates to a current vacancy.

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More about this job

Responsibilities

The Associate Director will lead clinical supply forecast planning and direct the Sales and Operations Planning (S&OP) processes to ensure cross-functional alignment. They are responsible for translating complex clinical trial protocols into executable supply plans while proactively identifying and mitigating supply chain risks.

Requirements

Candidates must possess a Bachelor's degree in Supply Chain, Engineering, Life Sciences, or Finance, with a Master's or MBA highly preferred. A minimum of 8 years of experience in production planning or supply chain within the pharmaceutical or biotech sectors is required, along with expertise in ERP/MRP systems and GxP compliance.

Skills

Supply Chain Planning
Sales and Operations Planning
Clinical Trial Protocols
Demand Forecasting
Supply Chain Risk Management
ERP Systems
MRP Systems
SAP
Perceptive RTSM
Data Analysis
GMP Compliance
Standard Operating Procedures
Budgeting
Financial Forecasting
Cross-functional Leadership

Benefits

Flex Benefits
Retirement Savings Program
4 weeks paid vacation
Personal Days
Variable Pay Bonus
Short Term Incentive
Equity-based long-term incentive program

Visa sponsorship

Not detected in the job text

Keywords

Supply Chain Planning
Precision Oncology
Radioconjugates
GMP
Radiopharmaceutical
Clinical Trial
S&OP
Demand Planning
Supply Strategy
Risk Mitigation
ERP
MRP
SAP
Perceptive RTSM
GxP
SOP
Budgeting
Financial Forecasting
Clinical Distribution
Import/Export Regulations
CAPA
Deviation Investigations
Change Control
Cell Therapy
Data Modeling

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