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Documentation Associate
Ref No.: 18-33507
Location: Dayton, New Jersey
Position Type:Contract
Job Category:Quality Assurance
Benefits:Medical Insurance
Hiring a Documentation Associate
Duration: Temp to Perm
Client Location: Fortune 500 Pharma Company in Dayton, NJ
Work Schedule: 8am - 4:30 pm (40 hrs)
Essential Functions
  • Perform sample log-in activity and organize the incoming samples for testing.
  • Prepare the Standard Test Procedures, Specifications, SOPs, and Protocols as assigned.
  • Prepare the change control documents and route for the approval with other departments.
  • Co-ordinate with the Analyst to provide the necessary needs as and when required.
  • Co-ordinate to load and pull the stability samples from the chambers.
  • Issuing control documents and maintaining the control documents.
  • Organize the Laboratory related documents and maintain/submit the documentation to QA for archival as and when required.
  • Comply with all regulatory/in-house requirements (may include but not limited to safety, house keeping, laboratory chemical waste, cGMP, cGLP, documentation) when performing the assigned activity.
  • Minimum Bachelor Degree ; BS Chemistry preferable
  • Minimum 3 to 5 years of experience in pharmaceutical analytical lab
  • Ability to learn quickly
To Apply for immediate consideration please send resume to Michael Estaris at and reference job #18-33507 in the Subject Line and indicate the best times to contact you (please include nights and weekends if needed).
**Candidates must complete background and drug screenings before starting any assignment.
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