Artech Information System LLC
At the dawn of the new millennium, a unique information technology company was born: HCL Technologies. As narrated in the video below, HCL Technologies has demonstrated remarkable growth through the recent economic downturn, emerging as one of only eight 21st century listed technology companies in the world to cross $1bn in Net Profit, $6bn in Revenue and $15bn in Market Capitalization.
Job Description
Responsibilities: Responsible for general laboratory and operational support. Must maintain GMP compliance within the assigned laboratory. Complete all training, written exams, and laboratory certifications. Communicate results of testing effectively, accurately, and in a timely manner. Work effectively with other laboratory team members. Demonstrate proficiency in computerized systems. Comprehend mathematical concepts such as logarithms, algebra, conversions, fractions, decimals, and rounding. Demonstrated ability to troubleshoot analytical methods and equipment. Demonstrated capability to perform technical review of laboratory testing results and to identify and investigate suspect results. Strong organizational skills and ability to multi-task across projects and activities. Must have the ability to understand and follow written procedures. Must be self-motivated and work with minimal direction. Utilize good judgment in making decisions within limitations of recognized standard methods and procedures. Must be able to temporarily work a flexible schedule to meet business needs. Must maintain certification within the assigned area. Must be able to train other analysts in the use of analytical instruments. Must be able to obtain and maintain multiple laboratory technique proficiencies (as dictated by laboratory and business needs). Must be able to handle multiple duties and projects at the same time and be able to work in a fast-paced environment. Must be viewed by peers, supervisors, and managers as having strong technical and/or leadership skills. Must be able to work any shift on a routine basis to provide training and coverage for other analysts as needed. Ability to work with hazardous chemicals safely while performing assays. Must physically be able to meet requirements of a laboratory environment. Qualifications:
BS in Chemistry, MS preferred. At least 6 years analytical laboratory experience in a GMP regulated environment for BS or 4 years with MS or PhD. Experience in parenteral drug product pharmaceutical manufacturing is a plus. Successful hands-on analytical testing experience in a GMP environment. Must have mastered at least four (4) analytical technologies, i.e., GC, HPLC, LC/MS, ICP, AA, FTIR, UV-VIS, RAMAN SPECTROMETER, ION Chromatography, etc.
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Responsibilities: Responsible for general laboratory and operational support. Must maintain GMP compliance within the assigned laboratory. Complete all training, written exams, and laboratory certifications. Communicate results of testing effectively, accurately, and in a timely manner. Work effectively with other laboratory team members. Demonstrate proficiency in computerized systems. Comprehend mathematical concepts such as logarithms, algebra, conversions, fractions, decimals, and rounding. Demonstrated ability to troubleshoot analytical methods and equipment. Demonstrated capability to perform technical review of laboratory testing results and to identify and investigate suspect results. Strong organizational skills and ability to multi-task across projects and activities. Must have the ability to understand and follow written procedures. Must be self-motivated and work with minimal direction. Utilize good judgment in making decisions within limitations of recognized standard methods and procedures. Must be able to temporarily work a flexible schedule to meet business needs. Must maintain certification within the assigned area. Must be able to train other analysts in the use of analytical instruments. Must be able to obtain and maintain multiple laboratory technique proficiencies (as dictated by laboratory and business needs). Must be able to handle multiple duties and projects at the same time and be able to work in a fast-paced environment. Must be viewed by peers, supervisors, and managers as having strong technical and/or leadership skills. Must be able to work any shift on a routine basis to provide training and coverage for other analysts as needed. Ability to work with hazardous chemicals safely while performing assays. Must physically be able to meet requirements of a laboratory environment. Qualifications:
BS in Chemistry, MS preferred. At least 6 years analytical laboratory experience in a GMP regulated environment for BS or 4 years with MS or PhD. Experience in parenteral drug product pharmaceutical manufacturing is a plus. Successful hands-on analytical testing experience in a GMP environment. Must have mastered at least four (4) analytical technologies, i.e., GC, HPLC, LC/MS, ICP, AA, FTIR, UV-VIS, RAMAN SPECTROMETER, ION Chromatography, etc.
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