However, to develop a new renewable energy source for domestic use and to bring same to consumers certainly require the most complex logistical effort.
This has led to the development of biofuels, bio-briquettes and other biomass related energy resources over the past two decades.
#Briqs biotechnology how to
These are (i) how to manage large amount of domestic and industrial wastes generated from ever-increasing population in the country, (ii) how to control/reduce over-dependence on non-renewable energy resources - oil and gas (Phan, 2016) as well as over-dependence on rapidly depleting forest resources - fuelwood and other biomass (Omaka, Nwabue, Itumoh and Okeke, 2013) - and (iii) how to reduce deterioration of the environment occasioned by the continuous use of non-renewable energy resources which has resulted to serious climate change and global warming (Kampa and Castanas, 2008 Riojas-Rodriguez, Romano-Riquer, Santos-Burgoa, and Smith, 2001).Īs a result of these aforementioned challenges, many researches are geared towards developing renewable energy resources and energy efficient technologies for domestic use. Qualified candidates should apply via USPS to:ĮMD Millipore is proud to be an Affirmative Action/EEO employer.Most countries of the world is facing three obvious challenges of human development. This position is eligible for the EMD Millipore Employee Referral Program. In the alternative, a Master's degree in Life Science, Biotechnology, or a closely related field and two (2) years of work experience in an FDA regulated environment.ĭemonstrated ability with cell culture testing gained through lab bench experience with TCID50 ĭemonstrated ability to write technical SOPs ĭemonstrated ability performing assay validation gained through lab bench experience in an FDA regulated environment andĭemonstrated knowledge of Lab Inventory Management Systems (LIMS), Trackwise, and electronic document management systems.Īll years of experience may be gained concurrently. The Associate Scientist s duties will encompass the following:ġ) Performing testing in accordance with SOPs and regulations (cGMP and GLP) Ģ) Maintaining complete and comprehensive records for study integrity ģ) Making detailed observations and documenting results Ĥ) Operating and maintaining lab equipment as required by SOPs and testing procedures ĥ) Performing peer review of assay bath/lab records to ensure Right First Time (RFT) Ħ) Utilizing applicable computer programs during testing and routing tasks (i.e., Word, Excel, Oracle, LIMS, BRIQS, etc.) ħ) Utilizing problem solving/trouble shooting skills Ĩ) Communicating deviations/events, progress, and interim results to Study Management ĩ) Informing supervisors of deviations or factors that may affect quality and accuracy of data ġ0) Maintaining a working knowledge of lab procedures and assays ġ1) Assisting with revisions to SOPs, laboratory records, and other documentation as assigned ġ2) Compiling company health and safety regulations and procedures ġ3) Train lower level associates on 96-well assays and scoring of viral CPE under a microscope ġ4) Using and training other associates on specialized equipment in the lab ġ5) Being familiar with Lab Inventory Management Systems (LIMS), Trackwise, and electronic document management systems andġ6) Performing face to face interaction with on-site clients.īachelor's degree in Life Sciences, Biotechnology, or a closely related field and five (5) years of progressively more responsible work experience in an FDA regulated environment.
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