Associate Specialist Manufacturing

Job Title: Associate Specialist Manufacturing 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: The Associate Specialist Manufacturing plays a key role in the production of Fusion Pharma’s radiopharmaceutical products at its Hamilton, Ontario facility. Working within an aseptic manufacturing environment, this position supports the end-to-end process—from material preparation and radiopharmaceutical dispensing through patient dose packaging—while maintaining strict GxP, EHS, and radiation safety standards. The role also contributes to equipment calibration, cleaning and clearance activities, documentation, troubleshooting, inventory control, and continuous compliance across manufacturing operations.   Responsibilities: • Work with the operations team to maintain the manufacturing area in aseptic conditions.  • Perform the manufacturing and dispensing of radiopharmaceuticals compounds, in an aseptic environment, from material picking to patient dose packaging.  • Keep accurate records within the production records book.  • Perform the isolator and laboratory periodic cleaning activities prior to initiate a production campaign.  • Perform the line and cleanroom clearance after a production run.  • Assist during the process troubleshooting and investigation activities.  • Perform the periodic calibration of manufacturing equipment(s).  • Adhere to the GxP, EHS and radiation safety practices, maintain excellent training and performance records.  • Assist the team during secondary and tertiary packaging, material receiving and inventory control activities.    Qualifications: • Post secondary degree in life-science (chemistry, biology, biochemistry).  • 2-4 years of experience in a GMP manufacturing environment and cleanroom operations (sterile manufacturing) is required.  • Experience with environmental monitoring programs is an asset.  • Proven experience in Sterile, injectable is a must, radiopharmaceuticals manufacturing and radiation safety training is preferred.  • Efficient in the use of MS Office Suite and computerized systems required.  • Ability to be detail-oriented, efficient, and collaborative with minimal supervision is required. Motivation and leadership skills, with strong work ethic, integrity, and stability in the workplace and ability to thrive in a fast-paced environment.  • Able to communicate/coordinate effectively with cross functional departmental staff.  • Ability to investigate issues, identify root causes analysis and define resolutions.   • Ability to organize, prioritize and deliver tasks & projects with a sense of urgency.   • Flexibility with work hours depending on production schedule.    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 inclusion and providing a workplace that is free from discrimination. AstraZeneca is committed to accommodating persons with disabilities. Such accommodation is availa