Validation Engineer/ Specialist

Responsibilities The Validation Engineer/ Specialist will beresponsible 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. Qualifications Bachelor degree in Engineering or Science 5 to 10 years of experience required in the medical device, biotechnologyor 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 communication 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. #J-18808-Ljbffr