Big data management for cloud-enabled geological information services
In this 2018 paper published in Scientific Programming, Zhu et al. review the state of big data in the geological sciences and provide context to the challenges associated with managing that data in the cloud using China's various databases and tools as examples. Using the term "cloud-enabled geological information services" or CEGIS, they also outline the existing and new technologies that will bring together and shape how geologic data is accessed and used in the cloud. They conclude that "[w]ith the continuous development of big data technologies in addressing those challenges related to geological big data, such as the difficulties of describing and modeling geological big data with some complex characteristics, CEGIS will move towards a more mature and more intelligent direction in the future."
Manager, QA (Audit)
Overview
People are at the center of who we are and what we do.
Are you seeking…
– A culture defined with the help of your voice?
– Recognition for your talent and continued growth opportunity?
– Upfront tuition assistance (eligible day one of employment)? …
Global Medical Director – Transplant
Responsible for development and implementation of global medical strategies that support worldwide commercialization in the therapeutic area of Solid-Organ and Cellular Transplantation. Based on an excellent understanding of the comprehensive science of Transplant Medicine, incumbent will take a leadership role in definition of medical strategies for New Product Development, Life Cycle Management and Strategic Business Development opportunity assessment while representing commercial Global Medical Affairs in project teams during their implementation.…
Associate Principal Scientist – GMP Laboratories
Merck & Co., Inc. Kenilworth, N.J., U.S.A. known as Merck in the United States and Canada, is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. The difference between potential and achievement lies in the spark that fuels innovation and inventiveness; this is the space where Merck has codified its legacy for over a century .…
cGMP Biomanufacturing Manager
Position Summary
Due to a recent promotion we have a rare opening for a cGMP Biomanufacturing Manager. Now is the chance to gain unparalleled experience by working on multiple products and technologies. As the cGMP Biomanufacturing Manager you will be joining a dynamic team environment and enjoy a highly visible role within Catalent! …
Group Leader Quality Control
Location US-OH-Cincinnati
Requisition # 18-20820 # Positions 1 Category Quality – Quality Control
Overview Responsible for overseeing the daily operations of the QC Analysts in a commercial non-OSD testing group by setting clear expectations around the delivery of the finished product and stabilty work load.…
Evidence-based design and evaluation of a whole genome sequencing clinical report for the reference microbiology laboratory
Reporting isn't as simple as casually placing key figures on a page; significant work should go into designing a report template, particularly those reporting specialized data , like that found in the world of pathogen genomics. Crisan et al. of the University of British Columbia and the BC Centre for Disease Control looked for evidence-based guidelines on creating reports for such a specialty — specifically for tuberculosis genomic testing — and couldn't find any. So they researched and created their own. This 2018 paper details their journey towards a final report design, concluding "that the application of human-centered design methodologies allowed us to improve not only the visual aesthetics of the final report, but also its functionality, by carefully coupling stakeholder tasks, data, and constraints to techniques from information and graphic design."
An Effective Solution to Data Integrity Issues
LabLogic's Laura radiochromatography data collection and analysis software is the ideal solution to ensure data integrity for metabolite profiling, quality control, compound purification or any other chromatography task.Associate Scientist (Quality Control) – 2nd Shift
Overview
People are at the center of who we are and what we do.
Are you seeking…
– A culture defined with the help of your voice?
– Recognition for your talent and continued growth opportunity?
– Upfront tuition assistance (eligible day one of employment)? …
FREDsense Technologies Selected by the Built in Canada Innovation Program to Deliver Water Testing Solutions
FREDsense Technologies Corp. is excited to announce the launch of a project supported by the Build in Canada Innovation Program (BCIP) through the Federal Government of Canada. FREDsense Technologies is an award-winning Calgary based company building next generation solutions for monitoring water quality in the utility, mining and environmental space. By creating portable hand-held instruments for water analysis, FREDsense is making it easier than ever to understand what contaminants are found in environmental water, allowing operators to better safeguard our environment.QIAGEN and Sentieon Partner to Advance Precision Medicine With Highly Efficient Variant-Calling Software
QIAGEN N.V. and Sentieon, Inc. today announced a collaboration to advance precision medicine by delivering Sentieon’s award-winning software for calling variants as part of QIAGEN’s industry-leading bioinformatics portfolio, supporting thousands of next-generation sequencing (NGS) labs.DNAnexus Launches NGS Clinical Trial Solution
DNAnexus, the global leader in biomedical informatics and data management, today announced the availability of its Clinical Trial Solution (CTS) which streamlines the use of next-generation sequencing (NGS) data in regulated clinical trials. The company also announced Almac Diagnostics, a global precision medicine company, as one of the first customers of the service.Director, Analytical Development
Job Description
Catalent San Diego is looking to hire a Director of Analytical Development to build and lead a team focused on the analysis of small molecule and peptide drug products. The Analytical Development team will be responsible for supporting early phase development activities such as analytical method transfer, test method development, product testing and phase appropriate validation.…
Saama’s Life Science Ecosystem Helps Partners Leverage Its Award-Winning Clinical Data Analytics Solutions Without Replacing Existing Vendors
Saama Technologies, a leading clinical data analytics company, has launched the Life Science Ecosystem for its partners. The Life Science Ecosystem facilitates complementary and tailored application of its award-winning Life Science Analytics Cloud (LSAC) to customers’ preferred systems and services vendors.The Hidden Power of Barcodes
Perhaps one of the most overlooked and under-implemented interfaces is the simple but powerful barcode. Barcodes have been around for many years in consumer spaces – but what can they do for a laboratory? The answer largely depends on what kind of technology is used: traditional barcodes or Radio-Frequency Identification (RFID).
Medidata Introduces New Edge Family of Products for Clinical Operations at SCOPE 2018
As clinical trials become more complex, sponsors and contract research organizations (CROs) are looking for a unified platform to help them overcome challenges such as dealing with disparate systems, complying with new regulatory requirements and managing an increasing variety and volume of data. Today at SCOPE, Medidata Solutions (NASDAQ:MDSO) is introducing the Edge family of products, a holistic suite of intelligent trial planning and management solutions that seamlessly address today’s operational and regulatory requirements.Medical Information Specialist
Leverage medical, scientific and product knowledge, clinical expertise, literature evaluation and writing skills to influence the successful adoption and utilization of CSL Behring products with Key Opinion Leaders, formulary decision makers, prescribers, other healthcare professionals (HCP), caregivers and patients. Be an expert resource in educating and training stakeholders about CSL products. …
Managing Cannabis Testing Lab Workflows using LIMS
With the increasing legalization of both adult recreational and medical cannabis, there is a need for robust and reliable cannabis analytical testing to ensure consumer safety and drug potency. Cannabis testing laboratories receive high volumes of test requests from cannabis cultivators for testing quantitative and qualitative aspects of the plant. As the volume of tests each lab performs increases, the need for laboratories to make effective use of time and resource management, such as ensuring accurate and quick results, reports, regulatory compliance, quality assurance and many other aspects of data management becomes vital in staying competitive. To achieve this, a Laboratory Information Management System (LIMS) can play a vital role in addressing the data management challenges, maximizing automation, and in complying with the regulatory requirements.
Laboratory Informatics Weekly Update – Volume 16, Issue 7
February 14, 2018 Laboratory Informatics Weekly Update Volume 16, Issue 7 In This Issue Upcoming Webinars 02/21/2018 - Software Validation: More Than Just the Vendor Documentation02/22/2018 - Practical Enterprise Architecture for the Laboratory03/01/2018 - Webinar: A Guide for Laboratory Systems Management, Part 4: LIMS/LIS, ELN, SDMS, IT & Education Blogs The Hidden Power of BarcodesManaging Cannabis Testing Lab Workflows using LIMSTips for SampleManager LIMS™ Instrument IntegrationSelecting an ELN to Maximize IP Protection Journal Articles Moving ERP systems to the cloud: Data security issuesThis 2017 paper by Saa et al. examines the existing research literature concerning the status of moving…Analytical Scientist
Analytical Scientist
Position Summary
Due to growth, Catalent is looking to recruit an Analytical Scientist to join our growing Quality Control group at our site in Winchester, KY.
The Analytical Scientist will work on method transfer, method verification and method validation under appropriate guidance in support of clinical development and commercial manufacturing.…
