Validation & Engineering Group, Inc.
MF01-091825 Process Engineer / Qualification
Validation & Engineering Group, Inc., De Pere, Wisconsin, United States
Overview
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. Position
Process Engineer / Qualification 3 days ago Be among the first 25 applicants Note:
The original posting includes multiple headings and duplicate lines. This version preserves the essential information in a clean, accessible structure. Responsibilities
Process Engineering activities for the Medical Device Industry. Development and execution of Validation Protocols. Qualifications
Bachelor\'s Degree in Science or Engineering. Minimum of 3 years 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 regulatory guidance. Experience with Process Engineering and the development and execution of Validation Protocols. Technical Writing skills and investigations processes. Available to work extended hours, possibility of weekends and holidays. Seniority level
Mid-Senior level Employment type
Full-time Job function
Strategy/Planning and Information Technology Get notified about new Process Engineer jobs in
Aibonito, Puerto Rico . Process Engineer (Troubleshooting/validation)
Senior Process Engineer / Senior Validation Specialist
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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. Position
Process Engineer / Qualification 3 days ago Be among the first 25 applicants Note:
The original posting includes multiple headings and duplicate lines. This version preserves the essential information in a clean, accessible structure. Responsibilities
Process Engineering activities for the Medical Device Industry. Development and execution of Validation Protocols. Qualifications
Bachelor\'s Degree in Science or Engineering. Minimum of 3 years 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 regulatory guidance. Experience with Process Engineering and the development and execution of Validation Protocols. Technical Writing skills and investigations processes. Available to work extended hours, possibility of weekends and holidays. Seniority level
Mid-Senior level Employment type
Full-time Job function
Strategy/Planning and Information Technology Get notified about new Process Engineer jobs in
Aibonito, Puerto Rico . Process Engineer (Troubleshooting/validation)
Senior Process Engineer / Senior Validation Specialist
We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.
#J-18808-Ljbffr