Experienced Technical Writer

Pharmaceutical company in North Western NJ seeks associate with several years of broad based, manufacturing or regulatory experience in the pharmaceutical field.  Must have demonstrated project management and interpersonal skills.  Qualified candidates must possess excellent communication skills (both written and verbal) with some technical and regulatory writing ability.  Experience in multi-tasking and prioritizing projects.  Ability to prepare large complex documents.  Any knowledge in the area of global post-approval Chemistry, Manufacturing and Controls (CMC) change regulations and in the content and structure of the CMC section of a Marketing Authorization (eg. NADA, MAA, IRD, JNDA, DMF etc.) would be highly desirable.  Also knowledge of SUPAC, changes to NDA, and NTA's are highly desirable.  Must have experience in writing variations.  Long term (2-3 year) contract position.  Bachelor's degree a must, Master's preferred.  Salary flexible. 

 

Please click here to apply for this position and type code KML in the comment area.