Skip to content
← Back to vacancies

Production Planner, Supply Chain Planning

For international applicants

Visa

Sponsorship not stated in the posting.

Ask the employer before you apply.

Your work rights

Get similar jobs with visa sponsorshipManufacturing jobs in Canada with visa sponsorship

By tapping “Email me jobs like these” you agree to our Terms and confirm you've read the Privacy Policy.

Once a week. We first email you a link to confirm; nothing is sent until you open it. One-click unsubscribe. Already have an account? Sign in

About the employer

AstraZenecaPosted on the employer’s careers page · astrazeneca.wd3.myworkdayjobs.com

Working in Canada

Possible country route: Employer-specific work permit. A job offer is usually needed for an employer-specific permit. The employer may need an LMIA or an exemption. Express Entry permanent residence is a separate process.

IRCC times depend on the work-permit category and application country. Use the live processing-time tool; employer LMIA processing, if needed, is separate.

What to check before applying
  1. Confirm permit and employer steps. Ask whether an LMIA or exemption applies to the offer.
  2. Check the application country. Use IRCC requirements and the current processing-time tool.
  3. Apply for the correct permit. A job offer alone does not authorise work or entry.
Official immigration guidance ↗

Reviewed 2026-10-14. Country routes are context, not a confirmation that this vacancy or your passport qualifies.


Description (EN)

Job Title: Production Planner, 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 Production Planner who brings a detailed and collaborative focus to join our team. In this role, you will be pivotal in coordinating Global clinical supply operations, aligning internal manufacturing sites with Contract Manufacturing Organizations (CMOs), and ensuring the seamless delivery of radiopharmaceutical investigational medicinal product (IMP) to patients.

Responsibilities:

  • Collaborate closely with the Clinical Supply Chain team, CMOs, and internal manufacturing sites to plan and schedule patient doses, calibration sample availability, and overall manufacturing operations.
  • Prepare and communicate weekly manufacturing demand reports to internal and external collaborators to help align operations and plan ahead
  • Maintain accurate data entry within planning systems and trackers to ensure real-time visibility and schedule accuracy. Perform regular data audits to support reliable reporting and operational planning.
  • Develop, draft, and maintain Standard Operating Procedures (SOPs) and Work Instructions for core departmental processes and supply activities to ensure GxP compliance and consistency.
  • Act as a key liaison between supply chain, quality assurance, and manufacturing partners to resolve scheduling bottlenecks
  • 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 management, Business Administration, Life Sciences, or a related field.
  •  2 to 3 years of experience in production planning, scheduling, or supply chain experience, preferably within the pharmaceutical, biotech, or clinical research sectors.
  • Strong command of ERP/MRP systems and advanced data management tools (such as Microsoft Excel, SharePoint, and workflow automation tools).
  • Familiarity with GMP (Good Manufacturing Practices) and Standard Operating Procedures within a regulated manufacturing environment.
  • Exceptional organizational skills, acute attention to detail, and proven ability to communicate effectively with external and internal stakeholders.
  • 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. 
  • Hands-on experience with ERP/MRP systems (e.g., SAP or specialized clinical supply management systems like Perceptive RTSM)
  • Advanced proficiency in Microsoft Excel (data modeling, automated trackers, complex formulas)

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 71,379.20 to 93,685.20.

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.

Hamilton, CanadaOpen in maps ↗

Never pay a recruiter for a job offer or a visa promise. Check the original posting and employer identity before sharing documents. Pay any legitimate government visa fees only through official channels.

Published 5 days ago

Similar vacancies