Site Quality Lead - Orlando, FL

Jubilant Radiopharma; Orlando (FL); Vor Ort; USD 110.000 - 150.000; Vollzeit

Benefits dieser Stelle

Annual performance bonus

Generous vacation

401K matching

Zusammenfassung

Jubilant Radiopharmacies seeks a Site Quality Lead to ensure radiopharmaceutical manufacturing meets FDA, cGMP, and internal standards. You will oversee quality systems, support sterile operations, and partner with operations, QC, and corporate quality to improve processes impacting patient safety.

The role requires detail orientation and strong quality compliance knowledge, with potential to act as Radiation Safety Officer.

Qualifikationen

• Bachelor's degree in a scientific discipline required.
• 3+ years in pharmaceutical quality assurance or quality compliance (sterile or radiopharmaceuticals) preferred.
• Strong knowledge of FDA regulations, cGMP, and quality systems.
• Experience with 21 CFR parts and data integrity standards; audit support experience.

Aufgaben

• Maintain and improve quality systems (CAPA, change control, deviations, complaints, document control).
• Support audits including FDA inspections and customer audits.
• Ensure timely completion of quality events and corrective actions.
• Review batch records, QC data, and manufacturing documentation for compliance.
• Collaborate with Production and QC to ensure aseptic processing standards.

Kenntnisse

Quality mindset

Analytical thinking

Technical writing

Independent work

Cross-functional collaboration

Ausbildung

Bachelors in Chemistry, Biology, Pharmacy, or Engineering

Tools

LIMS

MES

ERP

CDS

Jobbeschreibung

At Jubilant Radiopharmacies, we support patient care by producing and delivering high‑quality radiopharmaceutical products that help clinicians diagnose and treat disease. Our teams work with purpose, collaboration, and a strong commitment to safety and compliance. We value people, empower growth, and encourage a culture where individuals can do their best work.

Jubilant Radiopharmacies is proud to be certified as a Great Place to Work®, recognizing our commitment to a respectful, supportive, and people‑first culture.

Role Overview

We are seeking a Site Quality Lead to help ensure our radiopharmaceutical manufacturing operations meet FDA, cGMP, and internal quality standards. In this role, you will oversee quality systems, provide support to sterile manufacturing operations, and partner closely with operations, QC, and corporate quality teams. This position is an excellent fit for someone who is detail‑oriented, knowledgeable in quality compliance, and motivated to improve processes that directly impact patient safety.

Key Responsibilities

• Maintain and improve quality systems, including CAPA, change control, deviations, complaints, and document control.
• Support internal and external audits, including FDA inspections and customer audits.
• Ensure timely completion of quality events and implementation of effective corrective actions.
• Monitor compliance with 21 CFR Part 212 and applicable USP chapters.
• Review batch records, QC data, and manufacturing documentation for accuracy and compliance.
• Perform batch trend tracking and upload batch information required by customers.
• Support regulatory submissions and responses to health authority inquiries.
• May serve as the Radiation Safety Officer.
• Collaborate with Production and QC teams to ensure aseptic processing standards are met.
• Support root cause analysis and write investigation reports for quality events.
• Participate in environmental monitoring review, trending, and sterility assurance activities, including media fill validations.
• Develop and deliver GMP and compliance training.
• Write and update SOPs, protocols, and reports in alignment with regulatory expectations.
• Identify and implement process improvements that enhance quality and operational efficiency.
• Partner with Corporate Quality, Supply Chain, Radiation Safety, Engineering, and Operations to support site readiness and compliance.

Qualifications

• Bachelor’s degree in a scientific discipline (e.g., Chemistry, Biology, Pharmacy, Engineering).
• 3+ years of experience in pharmaceutical quality assurance or quality compliance, preferably in sterile or radiopharmaceutical manufacturing.
• Strong knowledge of FDA regulations, cGMP, and quality systems.
• In‑depth understanding of GxP regulations, FDA 21 CFR Part 11, 21 CFR Part 211, 21 CFR Part 212, USP <825>, and global data integrity standards.
• Experience with electronic systems such as LIMS, MES, ERP, or CDS.
• Strong communication, organization, analytical thinking, and technical writing skills.
• Ability to work independently and manage multiple priorities effectively.
• Ability to collaborate well with cross‑functional stakeholders.

We offer competitive compensation, an annual performance bonus, generous vacation, and 401K matching.

Equal Employment Opportunity Statement

Jubilant Radiopharmacies is an equal opportunity employer. We are committed to building a diverse and inclusive workplace where all employees feel valued and supported. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other legally protected status.