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Document Control/Junior Tech Writer

Job Attributes

Job Id:

25091

Job Category:

Clinical & Life Sciences

Job Location:

Summit, Nj, NJ  07901

Security Clearance:

No Clearance

Business Unit:

Piper Companies

JOB DESCRIPTION

Piper Companies is looking for a Document Control Consultant to coordinate and organize all GMP documents to assist with transitioning to a Electronic Batch Record System for a Pharmaceutical Manufacturer in Summit, NJ.

This is initially a 6 month consulting opportunity with possible extension or direct hire conversion. 

Responsibilities for the Document Control Associate include:

  • Provide Data Entry/Document Control/Tech Writing support for Quality Operations
  • Scan batch records
  • Organize GMP documents in Sharepoint
  • Work with SMEs on-site to gather documents and data
  • Ensure data is clearly organized in documents
  • Provide Technical Writing support 

Qualifications for the Document Control Associate include:

  • Industry experience (Biologics, Pharma, GMP)
  • Computer skills – Sharepoint
  • GMP experience is helpful, not required
  • Document Management/Technical Writing experience
  • Bachelor’s Degree

Compensation for the Document Control Associate include:

  • Hourly Range

Please send qualified resumes to Karen Pallone at kkpallone@pipercompanies.com

Apply Now

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New Search

Job Id:

25091

Job Category:

Clinical & Life Sciences

Job Location:

Summit, Nj, NJ  07901

Security Clearance:

No Clearance

Business Unit:

Piper Companies