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Senior Specialist, External Manufacturing

Job in Hamilton, Ontario, E8H, Canada
Listing for: AstraZeneca
Full Time, Seasonal/Temporary position
Listed on 2026-07-24
Job specializations:
  • Pharmaceutical
    Pharmaceutical Manufacturing, Validation Engineer, Quality Engineering, Regulatory Compliance Specialist
Salary/Wage Range or Industry Benchmark: 99552 - 130663 CAD Yearly CAD 99552.00 130663.00 YEAR
Job Description & How to Apply Below

Fusion Pharmaceuticals, a member of the AstraZeneca Group, is a clinical-stage oncology company focused on developing next-generation radio conjugates (RCs) as precision medicines. Fusion connects alpha particle emitting isotopes to various targeting molecules to selectively deliver the alpha emitting payloads to tumors. Fusion’s clinical portfolio includes FPI-2265 targeting prostate specific membrane antigen (PSMA) for metastatic castration resistant prostate cancer currently in a Phase 2 trial;

FPI-1434 targeting insulin-like growth factor 1 receptor currently in a Phase 1 trial; FPI-2059, a small molecule targeting neurotensin receptor 1 (NTSR1), currently in a Phase 1 trial; and FPI-2068, a bispecific IgG-based EGFR-cMET targeted radio conjugate currently in a Phase 1 trial. Fusion is pursuing combination programs between RCs and DNA Damage Response Inhibitors (DDRis) and immune-oncology agents. Fusion has a fully operational Good Manufacturing Practice (GMP) compliant state-of-the-art radiopharmaceutical manufacturing facility to meet supply demand for Fusion's growing pipeline of RCs.

Job Description

As the Sr. Specialist, External Manufacturing, you will support external manufacturing projects. You will facilitate scheduling meetings, follow up on project tasks, and track progress against key project milestones and KPIs. This position is located onsite in Hamilton, Ontario, Canada and requires a 5‑day per week on‑site presence.

Key Responsibilities
  • Collaborate with Contract Development Manufacturing Organizations (CDMOs), the internal manufacturing site, and the Clinical Supply Chain team to ensure drug supply is delivered on time.
  • Work with internal stakeholders to plan new material introduction activities within the master manufacturing schedule and provide regular updates on ongoing activities and project statuses.
  • Support cross‑functional planning and execution of tech transfer, scale‑up, process characterization, and validation (PPQ/PV). Ensure equipment/facility readiness, comparability, and robust control strategies.
  • Partner with QA to ensure GMP compliance, inspection readiness, data integrity, and robust deviation/CAPA and change control. Support internal and external audits and regulatory inspections. Assist in outlining and drafting Standard Operating Procedures (SOPs) and Work Instructions for departmental activities.
  • Support financial management of invoice approval for payment.
  • Perform other duties as required by the business.
Qualifications
  • Minimum BSc in chemistry, engineering, or health sciences.
  • 3+ years of experience in manufacturing, supply chain management, or project management within the pharmaceutical or radiopharmaceutical industry.
  • Strong organizational skills with a proven ability to manage multiple tasks and meet deadlines.
  • Excellent communication and interpersonal skills to work collaboratively with internal and external stakeholders.
  • Knowledge of GMP regulations and clinical drug supply processes is a strong asset.
  • Detail‑oriented with a proactive approach to problem‑solving.
  • Ability to work effectively in a fast‑paced, multidisciplinary team environment.
  • Willingness to take on new tasks and responsibilities as required.
Preferred Qualifications
  • MSc in chemistry, engineering, or health sciences.
  • Experience with CDMOs and familiarity with external manufacturing processes.
  • Ability to communicate effectively in Mandarin.
Salary and Benefits

Annual base salary for this position ranges from 99,552.80 to . 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.

Equal Opportunity Employer

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 AZCH

We are using AI as part of the recruitment process.

This advertisement relates to a current vacancy.

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Position Requirements
10+ Years work experience
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