Analytical Chemist – Princeton, NJ

12 months+

Pharmaceuticals (Cell Therapy)

• Establish and develop analytical methods. Work with Quality Control and other Operations groups to trouble-shoot and improve existing analytical methods.
•  Design experimental plans based on the defined deliverables, planning the activities to meet the project timelines by working closely with project managers.
•  Routine sample analysis to support process development.  In summary, the responsibilities include method establishment, development and routine sample analysis to support process development and pilot production.
• The analytical methods routinely used include A280, capillary Gel Electrophoresis (cGE), capillary Isoelectric Focusing (cIEF), ELISAs, liquid chromatography (U/HPLC) and quantitative PCR (qPCR).
• Hands-on exp with A280, cGE, cIEF, ELISAs, chromatography and/or qPCR and LARGE MOLECULE is a MUST.
• Working knowledge of GMP/ GLP regulations in cGMP/ cGLP manufacturing environment STRONGLY PREFERRED.
• Routine use of MS Excel, MS PowerPoint and MS Word is a MUST     excellent writing, communication and presentation skills a MUST.

 

PLEASE APPLY WITH 2-3 REAL WORLD EXAMPLES OF WHERE YOU HAVE THE ABOVE EXPERIENCE!

The ability to perform as a MOST IMPORTANT ASPECT OF LISTING (please highlight this experience thoroughly)