Gmp Training/document Control Specialist (bilingual English/spanish Required) Vacancy In Pl Developments

Hiring Organization / Company: Pl Developments
Basic Salary: To Be Discussed
Employement Type: Full-Time

Job Details:

Job Details



  • Bilingual English/Spanish required
  • Bachelor’s degree in scientific discipline, or equivalent 5+ years GMP training experience in pharmaceutical industry
  • Experience in training those who may not be familiar with cGMP concepts
  • Experience with the preparation and delivery of training materials
  • Excellent verbal and written communication skills
  • Microsoft Office skills in Windows, Excel, Word, Visio and PowerPoint
  • Ability to think strategically and manage multiple projects and tasks
  • Working Knowledge of Oracle and Agile a plus
  • Ability to proofread both English and Spanish documents to ensure there are no spelling or grammatical errors


  • Prepare cGMP training material for all PLD sites
  • Serve as the GMP Trainer and Coordinator for Annual and New Hire cGMP training
  • Circulate, track and close CRN’s in Agile associated with controlled documents
  • Revise controlled documents, initiate CRNs and conduct training as required
  • Implement the review of controlled documents by the Subject Matter Expert (SME) on a regular basis
  • Support Oracle Learning Management (OLM) activities as needed
  • Work with Document Control personnel to proofread new and revised documents in Agile, both English and Spanish documents
  • Review, verify and update content of corporate controlled documents as needed

Job Location Information:
City: Westbury
State: Ny
Country: Us
Location: Westbury, Ny 11590

Date Posted: 2021-07-21
Job Listing No# : 107141

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