Two95 International Inc.
Sr. Analytical Scientist
Two95 International Inc., Durham, North Carolina, United States, 27703
Title:Location:Duration:
12+ monthsRate:
$Open/hr.
Requirements
General Responsibilities:Plan and conduct analytical tests for drug development and transfer the methods to CDMO.Analyze and interpret data and prepare technical reports.Perform IQ/OQ/PQ and maintain lab equipment.Follow safety procedures and good laboratory practice.Must be able to work independently with limited guidance from external consultants or CEO (this role would report directly into the CEO).Qualifications:BS/MS with 10-12+ years of pharma industry analytical experience working within analytical development/validation to support solid oral dosage forms (small molecules), or Ph.D. with 5-7+ years.Excellent method development and validation skills and routine analysis on pharmaceutical materials (including potent compounds).Strong preference for an analytical scientist who has used a variety of analytical techniques/instrumentation - for example, particle size analysis, TGA, DSC, HPLC, FTIR, Powder XRD, SEM, HPLC (Agilent), Dissolution, UV-Vis.Strong preference for an analytical scientist who either has worked within a contract analytical lab working with external clients or has worked within a pharma company that outsourced some analytical work to external CDMOs.Ability to self-manage and take on new tasks.Ability to learn new analytical techniques by hands-on work and review of published data.Ability to multi-task and hit project timelines.Excellent oral and written communication skills.ANDA background a plus.Benefits
Note: If interested, please send your updated resume to (url removed) and include your salary requirement along with your contact details with a suitable time when we can reach you. If you know of anyone in your sphere of contacts who would be a perfect match for this job, we would appreciate it if you could forward this posting to them with a copy to us.We look forward to hearing from you at the earliest!
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12+ monthsRate:
$Open/hr.
Requirements
General Responsibilities:Plan and conduct analytical tests for drug development and transfer the methods to CDMO.Analyze and interpret data and prepare technical reports.Perform IQ/OQ/PQ and maintain lab equipment.Follow safety procedures and good laboratory practice.Must be able to work independently with limited guidance from external consultants or CEO (this role would report directly into the CEO).Qualifications:BS/MS with 10-12+ years of pharma industry analytical experience working within analytical development/validation to support solid oral dosage forms (small molecules), or Ph.D. with 5-7+ years.Excellent method development and validation skills and routine analysis on pharmaceutical materials (including potent compounds).Strong preference for an analytical scientist who has used a variety of analytical techniques/instrumentation - for example, particle size analysis, TGA, DSC, HPLC, FTIR, Powder XRD, SEM, HPLC (Agilent), Dissolution, UV-Vis.Strong preference for an analytical scientist who either has worked within a contract analytical lab working with external clients or has worked within a pharma company that outsourced some analytical work to external CDMOs.Ability to self-manage and take on new tasks.Ability to learn new analytical techniques by hands-on work and review of published data.Ability to multi-task and hit project timelines.Excellent oral and written communication skills.ANDA background a plus.Benefits
Note: If interested, please send your updated resume to (url removed) and include your salary requirement along with your contact details with a suitable time when we can reach you. If you know of anyone in your sphere of contacts who would be a perfect match for this job, we would appreciate it if you could forward this posting to them with a copy to us.We look forward to hearing from you at the earliest!
#J-18808-Ljbffr