Senior Supplier Quality Auditor

At RayzeBio, every day is an opportunity to ignite meaningful change. As a wholly-owned subsidiary of Bristol Myers Squibb, RayzeBio blends the nimble, pioneering spirit of an emergent biotech with the global expertise and resources of a leading innovator in oncology. Our mission is to develop transformative radiopharmaceutical therapies that offer new hope for patients living with cancer. Here, you’ll join a multidisciplinary team where your ideas are valued, your expertise is amplified, and collaboration is at the heart of everything we do. From day one, expect to make an immediate impact—on our science, on our teams, and most importantly, on patients.

About the role

The Senior Supplier Quality Auditor is responsible for leading the planning, execution, and reporting of supplier and service provider audits to ensure compliance with applicable cGMP/GxP regulations, internal procedures, and quality agreements. This role provides independent quality oversight of critical suppliers and supports supplier qualification and monitoring programs. 10-15% of travel may be required.

Responsibilities

• Plan, schedule, and conduct onsite and remote audits of suppliers and external service providers in accordance with the approved supplier audit program.
• Evaluate supplier compliance with applicable regulatory requirements (e.g., FDA, EMA, ICH), internal SOPs, and executed quality agreements.
• Document supplier audit observations and collaborate with suppliers and internal stakeholders to develop appropriate and effective CAPAs.
• Track supplier CAPAs to closure and verify timely implementation and effectiveness.
• Maintain complete and accurate supplier audit records and ensure timely communication of audit results and risk assessments.
• Support regulatory inspections and inspection readiness activities related to supplier oversight and audit programs.
• Provide guidance and training to suppliers and internal teams on supplier audit processes and GxP compliance expectations.
• Participate in continuous improvement initiatives related to supplier quality oversight and supplier audit processes.
• Domestic travel to supplier sites is required.

Requirements

• Bachelor’s degree in Life Sciences, Chemistry, or a related field or equivalent experience.
• Minimum of 7 years of experience in quality assurance, auditing, or supplier management within the pharmaceutical, biotechnology, or cGMP industry.
• Auditing experience within regulated biotech/pharma industry or equivalent in a GxP-regulated environment, with at least 3 years in auditing or quality assurance.
• Strong knowledge of global GxP regulations and standards (e.g., 21 CFR Parts 11, 210, 211; EudraLex Volume 4; ICH Guidelines).
• Experience conducting audits across GMP, GLP, and/or GCP domains.

Skills

• Proven ability to identify systemic quality and compliance risks.
• Excellent analytical, communication, and report-writing skills.
• Ability to work independently and manage multiple priorities.
• Ability to utilize AI tools to enhance individual productivity and quality of work.
• Strong technical writing skills for audit reports and regulatory documentation.
• Sound quality judgment and ability to work independently.
• Strong communication and stakeholder management skills.

Work Environment

The noise level in the work environment is usually moderate.

Pay

Remote - United States - US: $96,148 - $116,508. The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee’s work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience.

Benefits

Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment.

• Health Coverage: Medical, pharmacy, dental, and vision care.
• Wellbeing Support: Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).
• Financial Well-being and Protection: 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.
• Work-life Benefits Include Paid Time Off:
  • US Exempt Employees: flexible time off (unlimited, with manager approval), 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico, or Rayzebio employees).
  • Phoenix, AZ, Puerto Rico, and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays.
  • Based on eligibility, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs, and an annual Global Shutdown between Christmas and New Year's Day.

All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown.