Operator Trainer

All Job Posting Locations: San Lorenzo, Puerto Rico, United States of America Position Summary The Operator Trainer is responsible for performing manufacturing functions in compliance with GMP/QSR requirements, company policies, and safety regulations while also serving as a trainer for designated manufacturing areas. The selected candidate will complete a structured training, qualification, and learning curve process before fully assuming all responsibilities of the role. Key Responsibilities Perform manufacturing operations in accordance with established specifications, GMP/QSR regulations, safety requirements, and company procedures. Operate manufacturing equipment, perform machine setups, configuration changes, and basic preventive maintenance activities as needed. Verify batch components and ensure materials are available and accurately identified before production activities. Assemble products according to approved manufacturing specifications and procedures. Conduct product quality inspections and ensure compliance with established quality standards. Complete manufacturing documentation and production records accurately and in a timely manner. Perform batch reconciliation and support material transfers to designated production areas. Maintain clean and organized work areas to prevent product contamination and material mix-ups. Support Certified Operator Programs and ensure products are inspected and dispositioned according to Quality Assurance requirements. Adhere to all safety requirements and utilize appropriate personal protective equipment (PPE). Report safety concerns, quality issues, material shortages, defects, batch discrepancies, or any condition that may impact product quality or operational performance. Train and coach newly hired associates following approved training curricula, ensuring successful qualification and compliance with quality expectations. Support manufacturing teams with training related to specification updates, process changes, and new procedures. Monitor employee training records through electronic learning management systems and ensure certifications remain current. Coordinate and administer the Operator Certification Program for supported manufacturing areas. Lead Continuous Improvement events and support implementation of operational excellence initiatives, including EthIdeas programs. Demonstrate flexibility to become qualified in multiple manufacturing processes and support training activities across different shifts as business needs require. For Hemostasis operations, support material handling activities and shipment execution when required. Ensure compliance with environmental, health, safety, and occupational regulations, including ISO 14001 and OHSAS 18001 requirements. Communicate business-related concerns, opportunities, and operational improvements to management. Education & Experience High School Diploma required; college studies preferred. Minimum of two (2) years of direct medical device manufacturing experience. Certified in at least three (3) manufacturing processes or qualified in three functional manufacturing areas that do not require certification. Basic knowledge of chart interpretation preferred for Hemostasis operations. Required Skills & Knowledge Availability to work overtime, multiple shifts (1st, 2nd, 3rd, and/or 12-hour shifts), including weekends and holidays. Basic mathematical skills, including addition, subtraction, multiplication, division, and percentages. Basic computer proficiency and experience using Microsoft Windows, MES, HMI, Matrix One, and related systems. Basic mechanical aptitude preferred. Experience using calibrated equipment such as scales, templates, rulers, and metal detectors. Strong communication, leadership, coaching, and problem‑solving abilities. Ability to work effectively in a fast‑paced, highly regulated manufacturing environment. For Hemostasis operations, knowledge of Environmental Controls and Lock Out/Tag Out procedures is preferred. #J-18808-Ljbffr