• net2source
  • Jersey City , NJ
  • Non-Executive Management
  • Full-Time
  • 10 Bayside Terrace


Qualifications:
A.S. required / B.S. degree preferred in appropriate engineering/scientific field Minimum of 2 years post - degree experience in a cGMP environment (e.g. Production, Development, Process Engineering, Technical Services or related field) in pharmaceutical industry Previous experience in writing investigations for atypical events in a manufacturing environment Excellent written and verbal communication skills

Responsibilities:
The candidate will support laboratory deviations including identification of Point of Occurrence and/or Root Cause, identification and implementation of corrective and preventative actions, and potentially authoring the final incident/investigation. Additionally, the candidate will be responsible for providing quality and administrative support to the Laboratory Operations Technical Support Deviation Management Lead, consisting of handling SAP Quality Notification (QN) Processing and QN Corrective Action Preventive Action (CAPA) tracking (sustaining current process and process improvement). This individual is responsible for ensuring compliance in accordance with cGMPs, and GLPs, international regulations guidelines, and policies/procedures


* The salary listed in the header is an estimate based on salary data for similar jobs in the same area. Salary or compensation data found in the job description is accurate.

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