Scientist

Posted Yesterday
Be an Early Applicant
Hamilton, ON, CAN
In-Office
82K-108K Annually
Senior level
Biotech • Pharmaceutical
The Role
Support design and tech transfer of manufacturing and analytical processes for targeted alpha therapies. Perform lab work, analyze data, lead technology transfers, produce SOPs and validation documents, participate in validation/qualification, and support CMC investigations.
Summary Generated by Built In

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.

This position 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:

  • Min. MS with 5+ years of experience in product development and manufacturing; 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.
  • 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 [email protected].

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.

Skills Required

  • Minimum MS degree (or advanced degree) in organic or analytical chemistry, radiochemistry, radiopharmaceutical sciences, Pharmaceutical Science, Chemical Engineering, or related discipline.
  • 5+ years of experience in product development and manufacturing.
  • Experience in radiopharmaceuticals manufacturing and analytical method development and validation.
  • Experience with manufacturing process design using an automated synthesis unit.
  • Knowledge of radiation safety principles and dangerous goods regulations (e.g., CNSC, NRC).
  • Familiarity with GMP and clinical manufacturing process and equipment validation.
  • Strong interpersonal skills with demonstrated leadership in cross-functional projects.
  • Excellent written and verbal communication skills adaptable to varied partners and geographies.
  • Willingness and availability to travel to various locations (primarily in North America).

AstraZeneca Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about AstraZeneca and has not been reviewed or approved by AstraZeneca.

  • Fair & Transparent Compensation Pay is considered competitive across many roles when total rewards are factored in. Senior scientific and leadership bands are described with high ranges that reinforce competitiveness at upper levels.
  • Strong & Reliable Incentives Bonuses, equity eligibility in many salaried roles, and solid sales on‑target earnings with upside are emphasized as meaningful parts of compensation. These elements boost overall value even where base pay is not the very highest.
  • Retirement Support A 401(k) program with a strong company match and immediate vesting is repeatedly cited as a standout. Generous retirement support is viewed as enhancing the total package relative to peers.

AstraZeneca Insights

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The Company
HQ: Gaithersburg, MD
70,000 Employees
Year Founded: 1999

What We Do

We're transforming the future of healthcare by unlocking the power of what science can do for people, society and the planet.

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