For Manufacturing services in the Engineering area. WHAT MAKES YOU A FIT: The Technical Part: • Bachelor's Degree in Mechanical, Electrical, Industrial, Manufacturing, or Biomedical Engineering, or a related technical field, and 2–3 + years of experience manufacturing environment, including the generation and execution of validation protocols for manufacturing equipment. • Bilingual (English & Spanish). • Shift: 2nd shift (12:00pm-9:00pm) and according to business needs. • Experience in: • Generation and execution of validation protocols for manufacturing equipment. • Qualification, validation, and lifecycle management of manufacturing systems and equipment. • GMP documentation development, including protocols, reports, risk assessments, deviations, and CAPAs. • Manufacturing process support, troubleshooting, compliance, and continuous improvement initiatives. AS A PIECE OF FITS, YOU WILL: (The day-to-day on the job) Key Responsibilities include, but are not limited to, the following: • Support the creation, execution, and maintenance of qualification and validation activities related to manufacturing processes and systems. • Generate and maintain manufacturing and system documentation required to support process changes, equipment implementation, and compliance requirements. • Actively support the execution of validation and qualification protocols and generate supporting reports. • Provide ongoing support for daily manufacturing operations and process performance monitoring. • Support activities related to quality system processes and manufacturing compliance requirements. • Monitor manufacturing metrics and assist in identifying opportunities for improvement. • Coordinate qualification, validation, and protocol execution activities across Manufacturing, Quality, and Engineering teams. • Prepare, review, and maintain qualification protocols, validation reports, risk assessments, and other compliance-related documentation. • Support deviation investigations, CAPA activities, and data integrity initiatives to ensure regulatory compliance. • Monitor manufacturing yields, process performance trends, and key performance indicators to identify and support continuous improvement opportunities. WHO WE ARE: We are a Service Provider company different from the rest. We pride ourselves in how we treat the most important piece of our company's puzzle: you! We integrate Engineering, Construction, Maintenance, Utilities and Specialized Technical services across the Island (and in the US as well!). Our company is flexible, family-oriented and focused on our resources' well-being, while providing our Pharmaceutical, Medical Device and Manufacturing industry clients with top-notch quality talent. We're FITS! Are you the next piece?