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Curium Environmental Monitoring Coordinator in Maryland Heights, Missouri

About Company : Company was formed in 2017 through the union of IBA Molecular and Mallinckrodt Nuclear Medicine LLC. Company is a world-class nuclear medicine solutions provider with over 100 years of combined industry experience. We are proud to service over 14 million patients worldwide each year and strive to provide best-in-class quality products and exceptional, reliable service. Our diverse group of industry experts is unified under one strong and singular focus to develop, manufacture and supply SPECT, PET and therapeutic radiopharmaceuticals to customers around the globe. In fact, we have over 6,000 customers in over 70 countries world-wide. At Company , every single dose counts in helping doctors and patients diagnose and treat disease. That means every single employee counts toward meeting this unified objective to help each patient live Life Forward . We have an amazing team that lives by our core values every single day integrity, commitment and collaboration. Our North American headquarters is in Maryland Heights, MO. Come grow with us! Summary of Position: Perform assigned quality control or quality assurance activities in order to comply with applicable SOP's and cGMPs. Responsibilities include the direct coordination of technicians. Schedule: Monday through Friday 6:30 am to 3pm with some overtime required Essential Functions: Ensure a safe and quality working environment through training, awareness, and compliance to safety/Quality guidelines and SOP s. Perform monitoring lab equipment and techniques SAS, SMA, Met One particle counter, viable airborne monitoring active and passive, total airborne particulate sampling, viable surface monitoring, personnel monitoring, and membrane filtration of water samples. Assist in the training of less experienced technicians and monitor schedules. Act as leader in area of responsibility and ensures FDA, NRC, ALARA, and OSHA requirements. Ensures that all necessary testing is carried out by the required due dates. Ensure the proper maintenance of all equipment and instruments, the cleanliness of the department and premises. Investigation of laboratory or quality deviations and out of specifications, product failures, and customer complaints. Ensure proper documentation of all processes and procedures in accordance with cGMP guidelines. Perform all work in compliance with site quality, site safety and radiation protection guidelines. Collaborate with other team members to ensure quality tasks are performed in timely manner. Demonstrate flexibility in adjusting to changing priorities and schedules Attend mandatory trainings as required by site regulatory requirements and management. Ensure and document necessary training. Provide a team environment in which technicians are empowered to make appropriate decisions and encouraged to participate in projects. Support plant / team changes and initiatives, participate in continuous improvement efforts, including cost reductions and lean manufacturing initiatives. Support and participate in plant Quality initiatives. Assist with investigations, and perform other general duties associated with the position as required by supervision. Requirements: Bachelor Degree in Biology, Chemistry or related Science field, experience considered in lieu of a degree. Five years of overall experience required, quality control / production environment experience in a cGMP facility is preferred. Supervisory experience is preferred. Good interpersonal skills, hands on, analytical, and problem solving and decision-making skills. Excellent writing and verbal communications skills, analytical and problem solving skills Good computer skills, including utilizing personal computers and data entry programs. Ability to work independently and with others to accomplish goals and priorities. Flexibility and teamwork skills, high level of energy and regular, consistent attendance. Organizational Relationships / Scope: Has contact with all internal quality QA, QC, V

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