Jobs / Canada / Astrazeneca Pharmaceuticals Lp

Astrazeneca Pharmaceuticals Lp

Production Planner, Supply Chain Planning

Canada – Hamilton – Longwood Road South Posted today

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Skills this job asks for

Supply chainComplianceExcelSAP

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Sponsorship verdict

No sponsorship evidence yet

No government record and no wording either way. Not a refusal: ask the recruiter.

  • No government sponsor record hereNo government sponsor record covers this employer in this country.
  • The posting doesn’t mention sponsorshipSilence isn’t a refusal — ask the recruiter before investing much time.
  • No salary bar for this routeCanada has no single salary bar: the employer usually needs a positive LMIA.
  • Confirmed live todayWhen a source last listed this job as open.
Details and sources
No salary bar for this route
Canada has no single salary bar: the employer usually needs a positive LMIA. Pay at or above the provincial median wage + 20% (e.g. C$36.92/h in Ontario) puts it in the high-wage stream. Source: https://www.canada.ca/en/employment-social-development/services/foreign-workers/median-wage.html, rules effective 2026-07-17.

Canada: Express Entry no longer awards ranking points for job offers (since 25 Mar 2025); a job offer still counts toward Federal Skilled Worker eligibility.

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Before you apply

Sponsorship unknown

No register record and no sponsorship wording in the posting. Worth asking the employer before investing significant time.

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About the role

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: • 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 Are you interested in working at AZ, apply today! AstraZeneca is an equal opportunity employer that is committed to diversity and inc

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