QA Inspector (Production) 2nd shift role
Summary
A global leader in Clinical Supply, Catalent partners with sponsors to accelerate and scale their trials with innovative, flexible and reliable supply solutions. Catalent provides comprehensive and integrated services for sponsors and studies of all sizes with 25+ years experience spanning 5,000 studies in more than 80 countries.…
Senior Statistical Programmer
MedImmune is the worldwide biologics research and development arm of AstraZeneca. Here, you'll have the opportunity to make a difference in people's lives every day. As one of the world's premier biotechnology companies, our mission is centered on delivering life-changing products that advance world health, and help fight and cure disease.…
Medical Writer
Summary
Amicus Therapeutics is a biotechnology company at the forefront of advanced therapies to treat a range of devastating rare and orphan diseases. We are looking to hire an experienced medical writer to be based at our headquarters in Cranbury, NJ.…
Associate Director, Regulatory Submission Manager
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 .…
Medical Science Liaison-Ophthalmics Southeast
The Medical Science Liaison is a field based position and will serve as a scientific peer and resource within the ophthalmic medical community, and act as a scientific expert to his/her colleagues. This position will represent Sun Ophthalmics in the areas of IOP-lowering and topical NSAID therapeutics.…
Senior Scientist, Biologics
Position Summary (Biologics, Kansas City, MO)
The Sr. Scientist will report to Group Leader, Pharmaceutical Development
The main activities will be to provide and report data, as required by project contracts within the Biologics Department. The data may be used for submission in Regulatory packages, release and stability testing of clinical and animal trial dose forms and in support of development projects. …
Protocol Coordinator (NCI)
PROGRAM DESCRIPTION
Within the Leidos Biomedical Research Inc.'s Clinical Research Directorate, the Clinical Monitoring Research Program (CMRP) provides high-quality comprehensive and strategic operational support to the high-profile domestic and international clinical research initiatives of the National Cancer Institute (NCI), National Institute of Allergy and Infectious Diseases (NIAID), Clinical Center (CC), National Institute of Heart, Lung and Blood Institute (NHLBI), National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS), National Center for Advancing Translational Sciences (NCATS), National Institute of Neurological Disorders and Stroke (NINDS), and the National Institute of Mental Health (NIMH).…
Illumina Acquires Edico Genome to Accelerate Genomic Data Analysis
llumina, Inc. announced that it acquired Edico Genome, the leading provider of data analysis acceleration solutions for next-generation sequencing (NGS). Edico Genome’s DRAGEN® Bio-IT Platform (DRAGEN) uses field programmable gate array (FPGA) technology in conjunction with proprietary software algorithms to reduce both data footprint and time to results.Bruker Introduces ParaVision® 360 Preclinical Imaging Software and AVANCE® NEO Systems with Advanced Multi-Receive Architecture for MRI
At the International Society of Magnetic Resonance in Medicine Conference, Bruker announced the launch of the next version of its preclinical imaging software, ParaVision 360. It is the most advanced research-grade software for preclinical MRI, and has now also been extended to nuclear molecular imaging. ParaVision 360 enables sequential or simultaneous PET/MR measurements and analysis in one user-friendly environment.Fabric Genomics Expands Commercial Leadership With New Clinical Customers Across the Globe
-Fabric Genomics™, the global leader in clinical interpretation of genomic data, announced that its proprietary clinical genomics platform has been selected by 10 new commercial partners across four continents, including Africa, Asia, Europe and North America. The company’s software is allowing these organizations to provide genomics leadership and state-of-the art clinical genomics testing in their respective countries.LIMS Data Migration
When implementing a new LIMS, the question is not usually whether to migrate legacy system data, but how much data, in what manner, and why?
Laboratory Informatics Weekly Update – Volume 16, Issue 25
June 20, 2018 Laboratory Informatics Weekly Update Volume 16, Issue 25 In This Issue Upcoming Webinars 06/21/2018 - Learn how to improve Compliance, Productivity and Collaboration by attending a Free LABTrack ELN on-line webinar06/21/2018 - Webinar: A Guide for Laboratory Systems Management, Part 7: Laboratory Processes06/22/2018 - Learn how to improve Compliance, Productivity and Collaboration by attending a Free LABTrack LIMS on-line webinar06/27/2018 - Learn how to improve Compliance, Productivity and Collaboration by attending a Free LABTrack ELN on-line webinar Journal Articles Welcome to Jupyter: Improving collaboration and reproduction in psychological research by using a notebook systemJupyter Notebook, an…Global Marketing Manager
Qualified candidates should apply via email to careers@wpiinc.com
Summary/Objective:
The Global Marketing Manager will be responsible for strategy and execution of marketing activities across WPI markets to develop compelling value for the customer and brand recognition.
Essential Functions (Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions):
• Work closely with the commercial teams to Identify and address opportunities within multiple vertical markets by applying a multi-channel campaign approach. …
Scientist
Scientist Responsibilities:
Performs duties related to cell and tissue culture, bioprinting, compound dosing and analysis per established protocols
Will be responsible for new assay development and establishing standard operating procedures (SOPs)
Utilizes a range of assay technologies to characterize bioprinted tissue constructs, including ELISA, qPCR, viability and histology
Independently identifies and implements new assay technologies that have an impact on assay throughput and/or performance
Independently designs, executes, and performs basic analysis of experiments, including independent troubleshooting. …
Group Head, Regulatory Writing
The Group Head, Regulatory Writing will manage a team of Regulatory Writing associates and collaborate with other RWS Groups and Function Heads to coordinate the timely production of high quality deliverables.
Major Responsibilities:
1. Functional and Operational Manager for a group of associates. …
Welcome to Jupyter: Improving collaboration and reproduction in psychological research by using a notebook system
Jupyter Notebook, an open-source interactive web application for the data science and scientific computing community (and with some of the features of an electronic laboratory notebook), has been publicly available since 2015, helping scientists make computational records of their research. In this 2018 tutorial article by Friedrich-Schiller-Universität Jena's Phillipp Sprengholz, the installation procedures and features are presented, particularly in the context of aiding psychological researchers with their efforts in making research more reproducible and shareable.
Manager Safety intelligence & Compliance Job
Purpose
To contribute and support activities related to Adverse Event reporting and quality tasks in order to ensure consistency and compliance in all functions performed by Product Safety. To ensure maintenance and development of quality activities in Product Safety including, but not limited to, compliance tracking as well as various functions (e.g.…
Sr. Brand Manager, Ophthalmics (Glaucoma)
Sun Ophthalmics is committed to building a world class commercial team of passionate, ethical, and credible professionals that are committed to winning the right way and are accountable to their assigned objectives.
We focus on our customer’s needs, and bring them “concierge level” service at all times. …
Data Admin (Laboratory Execution System)
Seeking LES Data Admin with 5-8 years of experience for a large QC Paperless program
- This program is for one of the world’s global research-based pharmaceutical and healthcare companies
- World class team is involved in this program to achieve high value
- Well-structured working process is in place
- The latest LabWare LIMS modules are used as part of the Solution
- Training related to data configuration specifics and Method execution module shall be imparted as part of the project
Summary of the key responsibilities, Skills:
- Ownership, accountability and responsibility for the Test Method Configuration
- Work with business SMEs , LES Admins to understand the data provided
- Configuration of test methods, calculations in LabWare LIMS with ELN
- Configuration of various LIMS objects
- Experienced working with Method Execution module in LW LIMS with ELN
- Experience on Instrument interfacing and writing parsing scripts
- Working experience in writing complex SQL Queries
- Highly productive and able to manage time and prioritize tasks to meet timelines
Technical Skills:
- Mandatory:
- LabWare LIMS Version 6 or 7 , LabWare ELN,
- Method execution Module, LIMS Basic
- Desirable: Experience in development of Interfaces with LW LIMS and Instruments
- Good to have:
- Experience in LIMS/LES Implementation
- LW LIMS , ELN certification
- Knowledge on Lab processes, Test Methods
Soft Skills:
- Excellent in Verbal and Written communication
- Good in documentation
- Self motivated and ability to work independently
Languages:
- Mandatory: English ( Written and verbal )
- Good to Have: French (Verbal )
Functional Consultant (Laboratory Execution System)
Seeking LES – Functional Consultant with 5-8 years of experience for a large QC Paperless Program which:
- Is to be delivered for one of the world’s largest global research-based and science led healthcare company
- Provides World class working environment to achieve high value and high performance
- Has well-structured working process in place
- Provides the opportunity to work on the latest LabWare LIMS modules
Summary of the key responsibilities, Skills:
- Functional expert on Method Execution module in LW LIMS with ELN and has the functional business process knowledge gained in a Laboratory environment.
