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:
- QC Laboratory Equipment IOPQ Executions (USA Midwestern Region)
Qualifications:
- Bachelors Degree in Science orEngineering.
- Minimum of 3years of experience in direct pharmaceutical medical device or biotechnology industries.
- Must be fully bilingual (English / Spanish) with excellent oral skills.
- Must be proficient using MS Windows and Microsoft Office applications.
- Strong knowledge in cGxP and regulatory guidance.
- Experience executing IOPQ protocols including CSV andrelated with QC Laboratory equipment.
- Technical Writing skills and investigations processes.
- Available to work extended hours possibility of weekends and holidays.
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:
- QC Laboratory Equipment IOPQ Executions (USA Midwestern Region)
Qualifications:
- Bachelors Degree in Science orEngineering.
- Minimum of 3years of experience in direct pharmaceutical medical device or biotechnology industries.
- Must be fully bilingual (English / Spanish) with excellent oral skills.
- Must be proficient using MS Windows and Microsoft Office applications.
- Strong knowledge in cGxP and regulatory guidance.
- Experience executing IOPQ protocols including CSV andrelated with QC Laboratory equipment.
- Technical Writing skills and investigations processes.
- Available to work extended hours possibility of weekends and holidays.
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