Validation & Engineering Group, Inc.
Validation & Engineering Group, Inc (V&EG)
We are a leading services supplier providing solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.
Engineering Position (Process Engineer) We are seeking talented, dedicated individuals committed to the highest standards of ethics and integrity.
The role focuses on supporting drug substance operations and the execution of manufacturing and quality systems.
Support drug substance operations and execute manufacturing/quality systems, including design of operations and system requirements, procedures, deviation investigations, process monitoring, training, and new product introductions.
Organize, analyze, and present interpretation of results for operational issues and projects.
Qualifications
Engineering education background.
Experience in the development and/or manufacturing of bio‑processes.
Working knowledge of pharmaceutical/biotech processes.
Skilled in performance of GMP production operations.
Regulatory knowledge and interactions.
Organizational, technical writing, and presentation skills.
Project management skills.
Knowledge of control charting and basic statistics.
Seniority level Entry level
Employment type Full‑time
Job function Strategy/Planning and Information Technology
Location Guaynabo, Puerto Rico
#J-18808-Ljbffr
Engineering Position (Process Engineer) We are seeking talented, dedicated individuals committed to the highest standards of ethics and integrity.
The role focuses on supporting drug substance operations and the execution of manufacturing and quality systems.
Support drug substance operations and execute manufacturing/quality systems, including design of operations and system requirements, procedures, deviation investigations, process monitoring, training, and new product introductions.
Organize, analyze, and present interpretation of results for operational issues and projects.
Qualifications
Engineering education background.
Experience in the development and/or manufacturing of bio‑processes.
Working knowledge of pharmaceutical/biotech processes.
Skilled in performance of GMP production operations.
Regulatory knowledge and interactions.
Organizational, technical writing, and presentation skills.
Project management skills.
Knowledge of control charting and basic statistics.
Seniority level Entry level
Employment type Full‑time
Job function Strategy/Planning and Information Technology
Location Guaynabo, Puerto Rico
#J-18808-Ljbffr