Aseptic Radiopharma Production Lead

VetJobs; Indianapolis (IN); On-site; USD 124,000 - 151,000; Full time

Benefits offered by this job

Discretionary incentive cash

Stock opportunities

Job summary

RayzeBio is seeking a Manager of Production in Indianapolis to lead the radiopharmaceutical drug product manufacturing team, ensuring compliant, on-schedule production for clinical and commercial needs.

You will drive a culture of safety and quality in a GMP environment, manage daily production, and develop a high-performing team focused on reliable supply while collaborating across functions to meet corporate objectives.

Qualifications

• BS or MS in a scientific field or equivalent work experience.
• 5+ years in GMP pharmaceutical manufacturing, radiopharmaceutical or sterile injectable preferred.
• Strong leadership and communication skills.

Responsibilities

• Provide in-plant management of production personnel and ensure GMP compliance.
• Oversee daily production schedules and batch manufacturing of radiopharmaceutical injectables.
• Ensure aseptic technique and sterile manufacturing practices.
• Manage the cleaning and sanitization of the production clean suite.
• Support the development and implementation of a robust operator qualification program.
• Draft GMP documentation including but not limited to Batch Records, SOP's, Forms, Deviations, CAPA's, Change Controls and reports.
• Support investigations and implement corrective and preventative action plans.
• Monitor and manage production department KPI's related to performance and throughput of GMP radiopharmaceutical operations.
• Ensure compliance with NRC, EH&S and US/EU GMP regulatory guidelines as required.

Skills

Team leadership

GMP compliance

Communication

AI in ops

Education

BS or MS in scientific field

High School / GED

Job description

RayzeBio is seeking a Manager of Production in Indianapolis to lead the radiopharmaceutical drug product manufacturing team, ensuring compliant, on-schedule production for clinical and commercial needs.

You will drive a culture of safety and quality in a GMP environment, manage daily production, and develop a high-performing team focused on reliable supply while collaborating across functions to meet corporate objectives.