Validation Engineer/ Specialist

Validation & Engineering Group USA  (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. The Validation Engineer/ Specialist will be responsible of all validation activities for the assigned project. This project include the validation of multiple autoclaves and Temperature controllers.  Validation Scope may include: Validation Life Cycle, Execution, Technical Documentation, Process, GAP Analysis, Risk Assessment, C&Q activities, among others.    - Bachelor degree in Engineering or Science  - 5 to 10  years of experience required in the medical device, biotechnology or pharmaceutical industry (liquid dosage a PLUS). - MUST have experience validating autoclaves - Experience with Validation Life Cycle (Process, Packaging and Cleaning). - Experience and knowledge in regulations, including GMP. - Experience developing and conducting efficient processes to meet production demands. - Excellent technical writing and verbal communication skills are required. - Excellent detail oriented individual who can identify milestones. - Great interpersonal and communications skills. - Able to interact with all areas and clients. - Proficiency utilizing  MS Office Suite (Word, Excel and PowerPoint) is required. - Available to work extended hours, holidays if require.  - Must be available to travel and work non-standard shifts if necessary. - Only candidates who qualifies with all requirements will be evaluate. - Bilingual (Spanish & English) a plus but not necessary.  Validation and Engineering Group, USA  Inc. is an Equal Employment Opportunity employer.