Blood scientist

s www.globalchannelmanagement.com jobopeningsjobs(at)globalchannelmanagement.co mmust be able to work the following hours 6 30AM-6 30PM and have flexibility to work other shifts when necessary. Weekends and overtime are required.Blood scientist needs 1-3 years experience with QC GMPBlood scientist requires immunohematology procedures Previous hospital and or Blood Banking experience. Experience with analytical instrumentation such as ProVue and or VISION is preferred. Familiarity with the guidelines and regulations of FDA OSHA ISO and cGMP Manual dexterity to handle instruments complete repetitive motions and stand for long periods of time is required. Diligent use of PPEs (Personal Protective Equipment) to limit exposure to bloodborne pathogens is required. Excellent oral and written communication skills are required. Proficiency with the Microsoft Office suite of products (Excel Word PowerPoint Outlook). Blood scientist duties perform in-process and release testing of all types of BioVue cassettes and Gel Cards. assure compliance with company standards and applicable regulatory agencies. participate in failure investigations to help determine root cause track and trend data identify and suggest process improvements to improve business measures. perform testing within established timelines in accordance with current cGMP s. He She will participate in equipment maintenance calibration program. prioritize and handle multiple tasks and challenges at one time and have the ability to work in a team environment and provide customer focused results in an efficient manner. document results clearly and accurately as well as be able to interpret results by comparing results against appropriate specification requirements. perform data entry of critical product process information and test results to be used in trend analysis. maintain work areas and equipment as well as ensure calibration and maintenance of equipment is performed at designated intervals. adhere to departmental and Company SOP s and safety requirements as well as be accountable for notifying management of any out of specifications or abnormal trend in results in a timely manner. provide support during regulatory inspections. Edits documentation (i.e. Standard Operating Procedures test methods batch records). Understands and applies PE tools in daily work activities.

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