Radio Pharma Quality Control Supervisor at Pro Talent Group

Pro Talent Group, a division of MS-IL Staffing & Packaging, and its local client are NOW HIRING a full-time Radio Pharma Quality Control Supervisor in the Indianapolis, Indiana area!

Salary Range: $104.6k - 140.5k per year

Shift: 1st Shift

(Weekend work, early starts, or late ending times may be required.)

The Quality Control Supervisor, reporting to the Sr. Manager of Quality Control, will oversee quality control testing for radiopharmaceuticals. This role includes managing a team of QC chemists, ensuring regulatory and QA compliance, and maintaining high quality standards for product release. Additionally, the Supervisor will ensure that laboratory personnel adhere to Environmental Health and Radiation Safety standards in daily operations.

Job Duties & Responsibilities:

Team Management:

• Supervise and mentor a team of QC Chemists, assigning tasks and prioritizing workloads for timely and accurate product release.
• Foster a positive, collaborative environment within the lab and with external stakeholders.
• Coordinate workflow and projects with Management and Planning to optimize QC activities.

Continuous Improvement:

• Participate in method transfers from CMOs or internal teams, ensuring data accuracy.
• Identify and implement process improvements to enhance quality and efficiency in QC labs.
• Provide suggestions for analysis as new radiopharmaceuticals advance through regulatory stages.

Product Release & Studies:

• Perform analyses for new radiopharmaceuticals, raw materials, and components as needed.
• Collaborate with managers to ensure timely review of release documentation and resolve discrepancies.

Quality Assurance & Regulatory Compliance:

• Assist with lab equipment calibration, maintenance, and GMP readiness.
• Support internal audits and troubleshooting, implementing corrective actions to improve quality processes.
• Maintain documentation on data analysis and team KPIs, ensuring compliance with GMP, safety guidelines, and regulatory standards.
• Assist in reviewing Standard Operating Procedures (SOPs) and other documents.

Job Requirements & Qualifications:

Education and Experience

• BS in chemistry or related field with 9+ years of experience in pharmaceutical field OR MS in chemistry or related field with 7+ years of experience in pharmaceutical field.
• Experience testing in a quality control chemistry lab.

Preferred Education and Experience:

• Experience in radiopharmaceutical field
• Experience handling radioactive materials

Skills:

• Highly motivated and organized professional with the ability to work independently or in a team environment .
• Multi-disciplined scientist with GMP experience
• Experience with root cause techniques such as 6 M’s, 5 Why’s, fishbone, or similar preferred.
• Very personable with strong communication skills
• Ability to multi-task and prioritize work based on multiple work-flows.
• Good organizational skills are required.
• Work with multiple computer systems, including Microsoft Office, and chromatography systems.
• Excellent professional ethics, integrity, and ability to maintain confidential information .

Travel Requirements: Up to 10% of travel may be required.

Relocation Information: Must be willing to relocate to Indianapolis, IN. Company does offer a relocation package.

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