QC & Production Technician I: FDG/Naf Synthesis

RPMGlobal; Cleveland (OH); On-site; USD 34,440 - 37,195; Full time

Job summary

RPMGlobal in Cleveland, OH is seeking a QC/Production Associate I to operate radiosynthesizers for drug product production and use analytical equipment for quality control. You will perform FDG and NaF synthesis and QC procedures, verify materials per SOPs, and help maintain cGMP records.

Responsibilities include equipment qualification, routine maintenance, inventory management, and supporting QA investigations. Ability to work varied shifts and travel up to 5% is required.

Qualifications

• High school diploma required; associate’s degree in chemistry, engineering, or natural sciences preferred.
• Efficient in MS Office Suite.
• Ability to work various shifts and weekends.
• Detail-oriented, accountable, patient, organized, and team-oriented.
• Able to lift ~50 lbs. and travel up to 5%.

Responsibilities

• Operate radiosynthesizers for FDG and NaF production per SOPs.
• Operate QC equipment and perform quality control processes per SOPs.
• Ensure materials/reagents are within expiry and properly accepted.
• Maintain qualification and calibration of equipment; assist in basic maintenance.
• Complete cGMP documentation and assist QA investigations, CAPAs, deviations.
• Support inventory management and reporting of materials and supplies.
• Communicate with support resources to troubleshoot issues; participate in environmental monitoring.
• Maintain clean, safe work areas and comply with ISO-classified area requirements.

Skills

MS Office Suite

Detail-oriented

Team environment

Professional communication

Shift flexibility

Safety-conscious

Education

Associate's degree in chemistry or natural sciences

Tools

MS Office

Job description

RPMGlobal in Cleveland, OH is seeking a QC/Production Associate I to operate radiosynthesizers for drug product production and use analytical equipment for quality control. You will perform FDG and NaF synthesis and QC procedures, verify materials per SOPs, and help maintain cGMP records.

Responsibilities include equipment qualification, routine maintenance, inventory management, and supporting QA investigations. Ability to work varied shifts and travel up to 5% is required.