Please note that this is a 7 months contract position.
Qualifications: Minimum of a Bachelor's degree in Medical Technology, Clinical Laboratory Science or related field. Minimum of 5-6 years clinical / hospital experience working in Transfusion Medicine: Blood Bank or Donor Processing Center. Required to be ASCP certified minimally as MT; preferably SBB. Experience leading test method and/or equipment validation. Familiarity with the guidelines and regulations of FDA, OSHA, ISO and cGMP is preferred. Excellent oral and written communication skills are required. Proficiency with the Microsoft Office suite of products (Excel, Word, PowerPoint, Outlook). This is a day shift position and you must be able to work between the following hours 8:00AM-5:00PM.
Responsibilities: Under general supervision, lead activities for product and process changes. Perform root cause investigations of product failure and non-conformance investigations. • Plans, designs, and performs diagnostic assay support activities. • Suggests and implements improvements to methodologies, processes, products, and systems related to particular projects. • Prepares technical documents, including protocols, quantitative analysis, and summary reports. • Participates in scientific meetings and presents technical information. • Provide technical support for on-going Process Improvement Validation. • Assist in New Product Development activities. • Maintain working knowledge of cGMP requirements to ensure adherence to compliance policies and regulations.
Applicants must provide their phone number. Reference job number A319.