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curium jobs

Posted on 30th January 2020

Microbiology Supervisor

United States
Quality
Permanent
1402

About Curium

Curium is the world’s largest nuclear medicine company with more than a century of industry experience. We develop, manufacture and distribute world-class radiopharmaceutical products to help patients around the globe. Our proven heritage combined with a pioneering approach are the hallmarks to deliver innovation, excellence and unparalleled service.

With manufacturing facilities across Europe and the United States, Curium delivers SPECT, PET and therapeutic radiopharmaceutical solutions for life-threatening diseases to over 14 million patients annually. The name ‘Curium’ honors the legacy of pioneering radioactive researchers Marie and Pierre Curie, after whom the radioactive element curium was named and emphasizes our focus on nuclear medicine. The tagline ‘Life Forward’ represents our commitment to securing a brighter future for all those we serve: An enhanced quality of care for our patients. A trusted partner to our customers. A supportive employer to our valued team.

Summary of Position

The Microbiology Supervisor at the Maryland Heights facility is responsible for leading the Microbiology Department while managing in a cGMP environment. He/she must maintain operational compliance with U.S. and international regulatory agencies (i.e. FDA, NRC, BDB, DHSS, etc.). The Microbiology Supervisor will also oversee laboratory testing and provide resource and instrumentation allocation, conduct/review laboratory investigations, implement and monitor corrective actions.

The Microbiology Supervisor will monitor and maintain quality programs that provide assurance that test specifications are met for raw materials, components, finished products, intermediates, stability, and validation testing. The Microbiology Supervisor participates in the hiring process, ensures training, and administers and monitors the job duties of laboratory employees.

Essential Functions

  • While working in a cGMP environment, he/she must maintain operational compliance with U.S. and international regulatory agencies (i.e. FDA, NRC, Health Canada, OSHA, etc.)
  • Work cross functionally to coordinate testing schedules and communications in support of the weekly production activities and ensure QC testing and maintenance activities are completed per requirements.
  • Ensure team compliance with all policies, procedures and site/company regulations.
  • Support investigations of process or product failures and customer complaints. Author, and/or review all area quality and safety exceptions and investigation reports. Facilitate on time completion of all corrective action items assigned to area.
  • Work safely with radioactivity and ensure all direct reports maintain ALARA and manage their daily activities accordingly to ensure they meet their quarterly ALARA goals.
  • Set clear vision by ensuring goals and objectives are aligned with site strategies and managing each team member’s performance management.
  • Measure and communicate team progress against individual, team and site goals and Key Performance Indicators (KPI’s).
  • Maintain an acceptable level of 5S in the area and promote proper maintenance and cleanliness of the department areas of responsibility.
  • Assure compliance with department training and qualification.

Requirements

  • Bachelor of Science Degree in Microbiology, or other science related field, required.
  • Minimum 3 years of experience in a cGMP environment.

Preferred Experience:

  • Lean Leader/Operational Excellence/5S
  • Method development/validation of Endotoxin, Bioburden and Sterility test methods. Working Conditions:
  • Must work in a plant producing radioactive materials and requiring all employees to participate in safety programs designed to minimize potential and/or actual exposure levels.
  • Must be able to wear a variety of personal protective equipment.
  • Able to work in a team-based environment across all functional groups.
  • Close attention to detail required, must possess good hand-eye coordination.
  • May be required to sit or stand for long periods of time while performing duties.
  • Must be able to work outside of regular work hours.
  • Able to remain calm in emergency situations while directing other employees
  • Ability to follow procedures and enforce compliance with procedures
  • Responsibilities also include the ability to lift, walk, bend, stoop, push, pull, reach, and climb stairs without accommodation.

Disclaimer

The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of employees assigned to this position.

Equal Opportunity Employer

Curium is an equal opportunity employer and believes everyone deserves respect, dignity and equality.  All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.

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