PET Site Supervisor - Lead Operations & Compliance

Cardinal Health

Louisville (KY)

Hybrid

USD 82.000 - 117.000

Vollzeit

14 Tage+

Eine vollständige Bewerbung in einer Minute

Maßgeschneiderter Lebenslauf und Anschreiben – versandbereit.

Schaffe es an den ATS-Filtern vorbei

Benefits dieser Stelle

Medical, dental, vision coverage
401k savings plan
Paid time off
Parental leave

Zusammenfassung

Cardinal Health's Nuclear Manufacturing operations in Louisville, KY, produce time-sensitive radiopharmaceuticals in a highly regulated environment. The role will lead a small team, schedule production, manage budgets, and ensure cGMP and regulatory compliance to support patient treatment.

You will oversee performance reviews, collaborate cross-functionally, and drive project management for investigational drugs while maintaining safety and quality standards.

Qualifikationen

  • Bachelor’s degree in related field, or equivalent work experience preferred.
  • 4-8 years of experience preferred.
  • Ability to obtain and maintain current qualifications to include production and/or quality.
  • Demonstrated success in managing people and leading a team.

Aufgaben

  • Manages small group of staff to ensure manufacturing operations.
  • Generates reports as it relates to financial performance.
  • Acts as Project Manager for investigational new drugs.
  • Executes SOPs in accordance with cGMP requirements including GDP.
  • Maintains a sterile environment and performs general maintenance.

Kenntnisse

Staff management
Communication skills
Project management
Regulatory compliance
Physical capability
Cross-functional collaboration

Ausbildung

Bachelor’s degree in related field

Jobbeschreibung

Cardinal Health's Nuclear Manufacturing operations in Louisville, KY, produce time-sensitive radiopharmaceuticals in a highly regulated environment. The role will lead a small team, schedule production, manage budgets, and ensure cGMP and regulatory compliance to support patient treatment.

You will oversee performance reviews, collaborate cross-functionally, and drive project management for investigational drugs while maintaining safety and quality standards.

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