Associate Director, Supply Chain Planning

AstraZeneca GmbH; Hamilton; On-site; CAD 124,000 - 163,000; Full time

Benefits offered by this job

4 weeks paid vacation

Annual personal days

Flex benefits & retirement savings

Equity-based long-term incentive (if/当

Job summary

Fusion Pharmaceuticals, part of the AstraZeneca Group, is seeking an Associate Director of Supply Chain Planning in Hamilton, ON to lead clinical supply forecast planning and cross-functional alignment. You will steward global visibility, translate complex trial protocols into executable plans, and drive S&OP processes with manufacturing partners.

You will focus on risk identification and proactive communication, support budgeting, and ensure GxP compliance and SOPs across core processes.

Qualifications

• Bachelor-level degree in a relevant field with 8+ years in planning.
• Strong data analysis, risk forecasting, and communication to executives.
• Experience with GMP/GxP or regulated manufacturing preferred.

Responsibilities

• Lead S&OP meetings with cross-functional partners.
• Translate clinical trial demand into executable supply plans.
• Develop high-level demand and supply reports and long/short-range strategies.
• Identify supply risks early and drive mitigation plans.
• Align internal and external manufacturing with demand forecasts.
• Support budgeting and monitor financial forecasts.

Skills

Supply chain planning

Data analysis

ERP/MRP SAP

Excel

Cross-functional collaboration

Risk management

Time zone coordination

Executive presentation

Education

Bachelor's degree in Supply Chain/Engineering/Life Sciences/Finance

Master’s degree or MBA preferred

Tools

SAP

Perceptive RTSM

SharePoint

Workflow automation tools

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:

• GTAA Top Employer Award for 11 years
• Top 100 Employers Award
• Canada’s Most Admired Corporate Culture
• Learn more about working with us in Canada
• View our YouTube channel

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

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 [e-mail]

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.

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