Validation & Engineering Group, Inc. is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, among other services.

This position is required to support the clients automation systems, including QBAS.  Development of CSV report preparation, execution and engineering support for Control Systems, hardware & software. Mostly PLC for manufacturing area.

• Bachelor's degree in Engineering or Science (Computer, Electrical, Mechanical or Industrial).
• Minimum of five (5) years of experience required in the medical device or pharmaceutical industry.
• Self-starter, able to prioritize multiple tasks to meet strict deadlines and have sufficient knowledge developing and conducting efficient processes to meet production demands.
• Excellent technical writing and verbal communication skills.
• Proficiency utilizing MS Office Suite (Word, Excel and PowerPoint) is required.
• Knowledge in regulations, including GMP, QSR, and ISO requirements is necessary.
• Excellent problem solving, decision-making, and root cause analysis skills in addition to interpersonal skills.
• Ability to effectively communicate concepts, ideas and knowledge to upper management, other individuals, customers and/ or teams across the organization is required.
• Fully bilingual (Spanish & English).

Positions available for Puerto Rico. 

Validation and Engineering Group, Inc is an Equal Employment Opportunity employer.