Title: Sr. Analytical Scientist
Location: Research Triangle Park, NC
Duration: 12+ months
Rate: $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).
- BS/MS with 10-12+ years of pharma industry analytical experience working within analytical development/validation to support solid oral dosage forms (small molecules), 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 who 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 [email protected] 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 then, we would appreciate if you can forward this posting to them with a copy to us.
We look forward to hearing from you at the earliest!
