![]() ![]() General knowledge of compendia! microbiology requirements. Knowledge/Skills: Working knowledge and application of scientific principles and aseptic techniques. " Comply with Health, Safety and Environmental responsibilities for the position.Įducation: MS/BS Chemistry/Pharmacy or AA with equivalent experienceĮxperience: 0 (MS) -5 years applicable industry experience preferably in pharmaceutical microbiology " Assist other scientists, as necessary, for timely project completion and support other lab personnel as required. " Is familiar with Quality Systems such as: Compliance Wire, Trackwise, Documentum. " Provides written and verbal updates on projects and activities as required. Accurately report results, and provide detailed records of results and conclusions. ![]() " Maintain notebooks within GMP standards and SOPs. " Perform identification of microorganisms. " Perform USP water sampling and testing. " Perform environmental sampling and testing. These activities include compendia! microbial testing of raw materials, in process materials, and finished products within scheduled timelines. " Under the supervision of other scientists, carry out activities in support of the manufacturing of pharmaceutical products. Demonstrates potential for technical proficiency and scientific creativity. " Under the supervision of other scientists, works on problems of limited scope where analysis of data requires evaluation of identifiable factors. EXP IN ENVIRONMENTAL MONITORING OR GROWTH PROMOTION IS A PLUS. Requestor & Work Location Requested by: N/A Alternate: N/A Report To: N/A Phone: N/A Ext.:N/A Travel Required: How Much Travel? Report To Manager's Office Address 1001 US Highway 202 USRAR, Raritan, NJ 08869 United States Start Date: Work Days: Sun Mon Tue Wed Thu Fri Sat End Date: Start Time: 7:00 AM Total Reg Hours: 40.Description/Comment: - ONSITE - DURATION - 6 MONTHS - SHIFT - MON-FRIDAY 8:30 - 5PM. Conduct self-inspections of workstations and offices for hazardous conditions. Immediately report and correct, if possible, unsafe conditions, spills and near miss incidents. Attend applicable safety and environmental education and training programs and participate in Safety Committees and attend departmental safety and environmental meetings. The serologist will be familiar with QuidelOrtho's safety and environmental policies and perform work tasks and operations in compliance with all safety and environmental rules and regulations, and encourage co-workers to do so if uncertain, consults with supervisor. He/She will be accountable for reporting nonconformance's to management immediately. The successful candidate will adhere to departmental and QuidelOrtho 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. He/She will maintain work areas and equipment as well as ensure calibration and maintenance of equipment is performed at designated intervals. The serologist will document results clearly and accurately as well as be able to interpret results by comparing results against appropriate specification requirements. The successful candidate will have the ability to 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. This person will assure compliance with company standards and applicable regulatory agencies. Responsibilities: The serologist will be responsible for testing for part of a project validation of methods on our Immunohematology products. This is a 1st shift position, and you must have flexibility to work some weekends and over time as required. Proficiency with the Microsoft Office suite of products (Excel, Word, PowerPoint, Outlook). Excellent oral and written communication skills are required. Diligent use of PPEs (Personal Protective Equipment) to limit exposure to bloodborne pathogens is required. Manual dexterity to handle instruments, complete repetitive motions, and stand for long periods of time is required. ![]() Familiarity with the guidelines and regulations of FDA, OSHA, ISO, and cGMP is preferred. Qualifications: A Bachelor's degree in Medical Technology, Biology or a related field of study and a minimum of 1-3 years' experience within a cGMP environment. Job Description & Requirements Job Type: Recruited Resource - General Temp Number of Positions: 1 System Location: OCD - 6118 Created Date: Job Title: Medical Technologist Specialist - NJ CWR Type: W-2 Reason: Special Project ![]()
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