Production Lead

Scorpion Therapeutics; Indianapolis (IN); On-site; USD 85,000 - 125,000; Full time

Benefits offered by this job

Radiopharmaceutical production

GMP compliance

Aseptic practices

Radiation safety

Process validation

Team leadership

Job summary

RayzeBio is seeking a Production Lead to oversee daily operations in manufacturing radiopharmaceuticals, ensuring GMP compliance, radiation safety, and document control. The role emphasizes process validation and ongoing improvements, with responsibility for inventory management and team leadership.

On-site requirement in Indianapolis, IN, working in cleanroom conditions with radioactive materials. Strong knowledge of aseptic techniques and cGMP is essential for success in this role.

Qualifications

• 4-6 years GMP experience, preferably in radiochemistry or radiopharmaceuticals.
• Associate's or Bachelor's in STEM preferred.
• knowledge of aseptic processes, cGMP, and injectable/radiopharmaceutical manufacturing essential.

Responsibilities

• lead production team
• ensure GMP and radiation safety adherence
• review and revise technical documents
• support validation and process improvements
• assist with inventory management

Skills

GMP experience

Radiochemistry

Radiopharmaceuticals

Aseptic processes

cGMP

Injectable manufacturing

Team leadership

Education

Associate's or Bachelor's in STEM

Job description

Role

Production Lead overseeing daily operations in manufacturing radiopharmaceuticals at RayzeBio, supporting compliance, safety, and process validation.

Responsibilities

• lead production team
• ensure GMP and radiation safety adherence
• review and revise technical documents
• support validation and process improvements
• assist with inventory management

Requirements

• 4-6 years GMP experience, preferably in radiochemistry or radiopharmaceuticals
• Associate's or Bachelor's in STEM preferred
• knowledge of aseptic processes, cGMP, and injectable/radiopharmaceutical manufacturing essential

High Value

• radiopharmaceutical production
• GMP
• aseptic practices
• radiation safety
• process validation
• team leadership

Work Setup

on-site, with physical requirements including working in cleanroom environments with radioactive materials; relocation to Indianapolis, IN required.