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Scientist

  • Hamilton, ON
  • On-site
  • Posted Oct 23, 2026
  • 1 position

$82,378–$108,121 / year

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Employment type
Full-time
Experience level
Senior · 5+ years
Minimum education
Master’s degree
Apply by
Nov 6, 2026
Posting language
English
Working hours
40 hours per week

Job summary

The Scientist will lead the development and technology transfer of manufacturing and analytical processes for targeted alpha therapies. They are responsible for generating validation documentation, analyzing data, and supporting the CMC group during investigations.

Job details

Job Title: Scientist 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: Fusion Pharmaceuticals is opening the role of Scientist to support the design of manufacturing and analytical processes as well as the technology transfer, in-house and with CDMO partners. This role will report to the Associate Director of Process Development and Technology Transfer and requires collaborative skills, multi-tasking ability, and the desire to strive in a fast-paced environment. The successful candidate will bring a strong background in radiolabelling, radiometal chemistry and analytical method development, and have knowledge of manufacturing within the biotech or pharmaceutical industry. Responsibilities: Build and complete the laboratory work and tasks related to the development of manufacturing and analytical processes for targeted alpha therapies and related compounds. Analyze generated data and report outcomes to the project’s teams. Lead or support the technology transfer of newly designed manufacturing and analytical processes. Generate supporting documentation for newly designed processes such as development reports, standard operating procedures (SOP), work instructions, validation documentation (e.g.: process and equipment validation, validation report). Participate in validation and qualification activities for new clinical manufacturing processes and analytical methods, as necessary. Support the CMC group during investigations (non-conformance, deviation, out-of-specification). Qualifications: Minimum MS degree with 5+ years of experience in product development and manufacturing, which may include relevant graduate or academic experience; Advanced degree in organic or analytical chemistry, radiochemistry, radiopharmaceutical sciences, Pharmaceutical Science, Chemical Engineering, or related scientific discipline. Experience in radiopharmaceuticals manufacturing and analytical method development and validation preferred. Experience with manufacturing process design using an automated synthesis unit is an asset. Knowledge of radiation safety principles/dangerous goods and regulations (e.g. CNSC, NRC). Strong interpersonal skills are required, and the successful candidate will work in a cross-functional team and will be expected to take a leadership position in key manufacturing projects. Excellent written and verbal communication skills with an ability to adapt to various partners and geography. Meticulous, self-motivated, decisive, and independent with a willingness to work in a fast-paced environment. Available to travel to various locations (primarily in North America). 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 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 82,377.60 to 108,120.60. 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.

What you’ll do

The Scientist will lead the development and technology transfer of manufacturing and analytical processes for targeted alpha therapies. They are responsible for generating validation documentation, analyzing data, and supporting the CMC group during investigations.

Requirements

Candidates must hold at least a Master's degree in a relevant scientific discipline with 5+ years of experience in product development and manufacturing. Proficiency in radiochemistry, analytical method development, and knowledge of radiation safety regulations are required.

Benefits

  • Flex Benefits
  • Retirement Savings Program
  • Paid vacation
  • Personal Days
  • Variable Pay Bonus
  • Short Term Incentive
  • Equity-based long-term incentive program

Listed skills

  • Leadership · Preferred
  • Data analysis · Preferred
  • Communication Skills · Preferred
  • Cross-Functional Collaboration · Preferred

Other relevant skills

Identified from the job description. Confirm important requirements above.

  • Radiolabelling
  • Radiometal chemistry
  • Analytical method development
  • Process development
  • Technology transfer
  • Manufacturing process design
  • GMP compliance
  • Radiation safety
  • Data analysis
  • Standard operating procedures
  • Validation documentation
  • Cross-functional collaboration
  • Leadership
  • Communication skills
  • Automated synthesis
  • Standard Operating Procedure
  • Innovation
  • Chemistry
  • Pharmaceuticals
  • Collaboration
  • Interpersonal Communications
  • Self-Motivation
  • Investigation
  • New Product Development
  • Manufacturing Processes
  • Verbal Communication Skills
  • Multitasking
  • Decisiveness
  • Oncology
  • Analytical Chemistry
  • Chemical Engineering
  • Biotechnology
  • Analytical Method
  • Geography
  • Process Development
  • Technology Transfer
  • Pharmaceutical Sciences
  • Radiation Protection
  • Radiopharmacology
  • Radiochemistry
  • Certified Nutrition Support Clinician

Job areas

  • Science & Research
  • Manufacturing
  • Healthcare
  • Engineering
  • Scientist
  • Drug Formulation Scientist
  • Pharmaceutical Technicians and Assistants
  • Medical Scientists, Except Epidemiologists

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