Site Quality Director

AstraZeneca • Hamilton, ON

1d • CA$146,404 - CA$192,155 • Onsite

About The Position

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, state‑of‑the‑art radiopharmaceutical facility in Hamilton, we’re turning cutting‑edge 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! This role is 5 days per week onsite. Provide strong site leadership and oversight to ensure responsibilities regarding QA, QC and site compliance activities. The position is accountable for assuring the supply of radio conjugate quality products to markets and ensuring cGMP compliance at the site. Responsible for leading, directing, identifying and setting quality goals, objectives, and perfect execution in alignment with Global Quality Goals. Maintain cGMP compliance at site, including harmonization of procedures in alignment with Global Policies & Standards. Ensuring the materials and products are tested and released in a timely manner by adhering to approved procedures and specifications. Acts as a champion for building a “Culture of Quality” across the organization. Accountable to assure site is always ready for all regulatory inspections. This role will report directly to the Head of Quality, Radiopharmaceutical.

Requirements

• Bachelor’s degree in chemistry, pharmacy or relevant engineering or life science field is required.
• This position requires a minimum of fifteen (15) years of experience (10 years + 5 years in leadership capacity) in pharmaceutical quality management, and minimum five (five) years of experience in leadership role.
• A strong knowledge of GMP’s in both domestic and international regulatory environments is required.
• Excellent and detailed knowledge of Quality/Compliance processes and programs for development and commercial products including regulatory requirements on a global level; working knowledge of safety and environment regulations and guidelines are also required.
• Strong comprehensive knowledge of USFDA 21 CFR regulations Part 11: EC/ER requirements, GMP requirements of various regulatory bodies – USFDA/ MHRA/ EU GMP/ PMDA.
• Strong comprehensive knowledge of ICH Guidelines, FDA and Health Canada Regulations.
• A proven ability to lead, manage and motivate people with a variety of skill sets is required.
• Strong organizational, interpersonal and communication skills are required.
• Knowledge of quality operations and compliance of clinical and commercial aseptic manufacturing.
• Must possess excellent written, organizational and communication skills.

Nice To Haves

• Candidates with advanced degrees are highly preferred.
• Significant experience in radio conjugates is preferred with experience in the review and auditing of executed batch records, material release records, and qualification protocols.
• Ability to work effectively in an international matrixed organization is strongly preferred.

Responsibilities

• Ensure all finished products intended for use in the market are safe and effective as per cGMP requirements, regulatory commitments, AZ policies & procedures and site SOPs.
• Set site quality goals, objectives and strategic direction in alignment with Global Radio Conjugate Quality goals.
• Track, trend, maintain and report all Quality and business metrics to monitor and action all QA & QC compliance activities.
• Prevent Quality or regulatory non-compliance issues which could lead to product stock-out or withdrawal, product approval delays or which would negatively impact the quality, financial performance and reputation of the company. Non-compliance issues are to be addressed via corrective and preventive actions (CAPA).
• Ensure rationalization and management of Quality processes, operations and systems. Perform gap analysis to plan actions for continuous improvements.
• Resource planning and monitoring for head count projections, manage site budget, capital budget and manage organizational development.
• Responsible for site lean design and execution of continuous Quality & Compliance improvement initiatives, standardizations and efficiency gains to enhance compliance, drive efficiencies and reduce cost of poor quality.
• Coach and develop direct and indirect reports, as appropriate, through ongoing, example-based performance feedback, annual performance reviews and the provision of training and development opportunities.
• Performs all work in support of our Corporate Values and Behaviors and in accordance with established regulatory and compliance and safety requirements.
• Ensure the raw material, packaging material and finished products are tested and released in accordance to approved specification and test methods in a timely manner as per the site commits and support business needs.
• Ensure the health authority and Annex 1 requirements at the site are met for sterile products.
• Support the development of site strategy to respond to audit observations, inspection findings and implement corrective actions.
• Create and maintain 24/7 inspection readiness at the Hamilton site.
• Be a solution-oriented leader and role model AZ behaviors.
• This is a supervisory position with direct reports; therefore, this position will establish goals and objectives, prepare performance appraisals, monitor/review work product and coach/mentor direct reports.
• Other duties as required/assigned.

Benefits

• Annual base salary for this position ranges from 146,404.00 to 192,155.25.
• Annual Variable Pay Bonus/Short Term Incentive opportunity
• Eligibility to participate in our equity-based long-term incentive program (if applicable to role).
• Competitive Flex Benefits & Retirement Savings Program
• 4 weeks’ paid vacation
• annual Personal Days
• Contract Benefits Program (for Fixed Term Contract/Temporary positions excluding students)

What This Job Offers

• Job Type: Full-time
• Career Level: Manager