We are currently seeking an Analytical Study Monitor for a 9+ month contract in RTP:
The selected candidate will work closely and collaboratively within the global team of residue analytics and will specifically be conducting the following tasks:
•Coordinate/monitor multiple residue studies (the analysis of field trial residue samples, method validations, independent method validations, storage stability studies and others). Ensure the analysis is conducted under GLP and as per EU or USEPA ...
My name is Donald and I represent The Fountain Group. We are a national staffing firm and are currently seeking a Data Reviewer for a prominent client of ours. This position is located in Holly Springs, NC. Details for the positions are as follows:
Operational Phase Support organization of the QC Analytical, Biochemistry, and Raw Materials laboratory.
Plan and assist with required resources for day to day data review of raw data generated in the QC laboratories ...
Laboratory Technical Specialist
Our company is looking for an experienced Laboratory Technical Specialist to perform BSI database, lab quality assurance, and DNA activities.
In conjunction with the study staff, lab director, and senior laboratory technical specialist, communicate directly in a professional manner with clients such as the National Institute of Environmental Health Sciences (NIEHS).
Communicate in a professional ...
Support operations by providing analytical testing for materials and products, including data.
Perform dissolution, assay, content uniformity, related compounds/impurity analytical testing using HPLC and UV.
Testing is performed in a GMP environment, primarily testing solid oral dosage forms (tablets and capsules).
Generate GMP documentation in support of the testing performed.
Entry level to several years will be considered.
Testing experience ...
• Support operations by providing analytical testing for materials and products, including data.
• Perform dissolution, assay, content uniformity, related compounds/impurity analytical testing using HPLC and UV.
• Testing is performed in a GMP environment, primarily testing solid oral dosage forms (tablets and capsules).
• Generate GMP documentation in support of the testing performed.
• Entry level to several years will be considered.
• Testing experience in ...
This position will support the organization of the QC Biochemistry laboratory at the Flu Cell Culture facility in Holly Springs, NC.
Primary responsibilities for this position include method development and validation for biochemistry assays (protein content determination by BCA, SDS-PAGE, ELISA, and UV/Vis spectrometry).
Perform and assist in the method development and validation Author SOPs, protocols and technical reports
Perform laboratory testing associated ...
Support functions of the QC Sample Management group as assigned, including, one or more of the following:
Assist in the coordination and scheduling of all QCSM equipment PM's and CM's
Assist in distribution of all samples destined for various QC labs on 24/7 basis
Total QCSM throughput averages over 450 samples per month and is forecasted to increase with Bulk, Fill Finish, and Pilot Plant operations coming online
Support third party contract lab shipping of QC ...
Jan 23 -
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