Documentation Coordinator - GMP, batch records, SOPs in Cranbury Township, NJ at Apex Life Sciences

Date Posted: 6/23/2018

Job Snapshot

Job Description


DOCUMENT COORDINATOR

Pharmaceutical Industry

QUALIFICATIONS:

  • Working knowledge of Microsoft Office programs.
  • Detail oriented, well-organized, have knowledge of good documentation practices, and knowledge of scientific terms and (preferably) change request forms.
  • Ability to apply deductive reasoning and understand complicated issues.
  • Ability to receive and follow written and verbal instructions.
  • Ability to follow safety and security practices.
  • Ability to meet deadlines
  • Maintain confidentiality of certain information.
  • High school diploma or equivalent. College degree not required but preferred.
  • Some administrative experience with scanning, filing and organization.

ESSENTIAL FUNCTIONS:

  • Creating a detailed inventory of all documents/notebooks/binders (Documents) in the document room.
  • Reviewing all of the Documents in our controlled room and determining which Documents should be sent off-site verses internal storage.
  • Organizing Documents by appropriate category (to be determined).
  • Create an electronic database of the Documents so that Documents can be easily searched and retrieved.
  • Scanning of Documents and usage of change request forms.

FOR IMMEDIATE CONSIDERATION PLEASE CALL TELECA OGELE AT 732-636-1497 AND EMAIL YOUR RESUME TO TOGELE@APEXLIFESCIENCES.COM