Validation & Engineering Group Inc. (V&EG) is a leading services supplier who provides solutions for the Pharmaceutical Biotechnology Chemical Food and Medical Devices industries in the following areas: Laboratory Compliance Computer Engineering Project Management Validation and other services.
We are seeking a talented dedicated individual committed to work under the highest ethics standards for the following position:
- Technical Writer / Validation Specialist
Job Summary
We are seeking one Technical Writer / Validation Specialist to support C&Q document development. The ideal candidate has experience working with CDOCS and Kneat and can leverage existing documentation to develop validation deliverables.
Key Responsibilities
- Use existing documentation as a baseline to support new document development
- Develop CCMS narratives and draft validation lifecycle documentation
- Ensure documentation aligns with project and quality requirements
Qualifications
- Experience as a Technical Writer and/or Validation Specialist
- Hands-on experience with CDOCS and Kneat
- Familiarity with validation lifecycle documentation in regulated environments
Required Experience:
IC
Validation & Engineering Group Inc. (V&EG) is a leading services supplier who provides solutions for the Pharmaceutical Biotechnology Chemical Food and Medical Devices industries in the following areas: Laboratory Compliance Computer Engineering Project Management Validation and other services.We ar...
Validation & Engineering Group Inc. (V&EG) is a leading services supplier who provides solutions for the Pharmaceutical Biotechnology Chemical Food and Medical Devices industries in the following areas: Laboratory Compliance Computer Engineering Project Management Validation and other services.
We are seeking a talented dedicated individual committed to work under the highest ethics standards for the following position:
- Technical Writer / Validation Specialist
Job Summary
We are seeking one Technical Writer / Validation Specialist to support C&Q document development. The ideal candidate has experience working with CDOCS and Kneat and can leverage existing documentation to develop validation deliverables.
Key Responsibilities
- Use existing documentation as a baseline to support new document development
- Develop CCMS narratives and draft validation lifecycle documentation
- Ensure documentation aligns with project and quality requirements
Qualifications
- Experience as a Technical Writer and/or Validation Specialist
- Hands-on experience with CDOCS and Kneat
- Familiarity with validation lifecycle documentation in regulated environments
Required Experience:
IC
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