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CQV Technical Writer

  1. North America, United States
North Carolina
  1. Contract
Competitive
  1. Commissioning, Qualification and Validation
36094

This vacancy has now expired

CQV Technical Writer - Pharmaceuticals - North Carolina - 12-Month Contract 

Our client, a global pharmaceutical manufacturing organization are looking for a talented CQV Technical Writer to join their expanding team. With continued organizational growth and considerable investment across their portfolio and capital programs this is an extremely exciting opportunity to contribute towards their brand-new manufacturing facility on the East Coast of the United States.

Responsibilities: 
  • Support CQV through all phases of the Project for cGMP Documentation generation and execution.  This includes but not limited to: CQV Validation Master Plan, Validation Project Plans, System Impact Assessment Report, URS’s, DQ’s, RTM’s, QRA’s, PPPS’s, FAT protocols, IV protocols, OV protocols and all Final and Summary Reports.
  • Act as CQV SME on all queries relating to all CQV cGMP Documentation both generated documents and executed documents.
  • Ensure all cGMP documentation deliverables are met.
  • Arrange and coordinate all facilitated reviews relating to all cGMP documents.
  • Where required, coordinate and support system to ensure full approvals for CQV pre-req documents.
  • Coordinate daily deliverables for cGMP documentation generation team
  • Collaborate with cross-functional teams to develop and/or edit CQV validation documentation including, but not limited to URS’s, DQ’s, RTM’s, VMP’s, VPP’s that define system and equipment requirements.
  • Review and approve CQV validation documents to ensure they are clear, concise, and meet regulatory standards.
Requirements: 
  • 5-10 years in a similar technical writing role for cGMP Documentation.
  • Minimum 5 years documentation management experience on Large Scale Projects.
  • Experience with liaising with other departments and engineers/QA, ensuring streamlined processing of project documentation or similar type documentation process.
  • Willingness to take action in a proactive manner for driving progress.
  • Strong communication skills.
  • BA/BS in a related field and 5+ years experience successfully executing complex projects in a Pharma/cGMP environment.
  • Emphasis for this hire is on attitude (Positive Can-Do attitude) and strong collaboration.
  • Acts with detail-driven ownership and follow through.
If this role is of interest to you, please apply now! 
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