Job DescriptionPerform quality control tests for Media raw materials, intermediate and final products, as well as laboratory internal controls. Perform environmental monitoring sampling and testing. Follow Good Laboratory Practices, Good Manufacturing Practices, Good Documentation Practices, and safety measures, assuring best practices for reliability of results.ResponsibilitiesEssential Functions & Accountabilities:Executes analysis on raw materials for Incoming Quality, intermediate and finished goods for Final Release.Executes laboratory internal controls.Collaborates with the test required as part of equipment qualification and method validations.Records results on inspection forms and reports. Maintains department files for readily retrievable access of records.Notifies designated supervisor or engineer when result exceeds acceptable limits or when major incidents are noted.Coordinates external testing, samples shipment, tracking and test results report, review.Performs tasks under Good Manufacturing Practices (GMPs), Good Laboratory Practices (GLP), Good documentation Practices (GDP), safety techniques and aligned with the regulatory standards such as USP, ACS, Ph. Eur, ASTM for laboratory testing and improvements.Performs environmental monitoring sampling and testing or coordinates with contractors when required.Collaborates with Lean initiatives such as 5S and Gemba walks.Collaborates with inventory tracking and notifies the supervisor to maintain the stock of materials.Collaborates in training of new personnel in specific testing when required.Executes cleaning activities to maintain order and disinfection of specific areas.Performs equipment user´s preventive maintenance and documents appropriately.Collaborates in documentation improvement, such as SOPs, forms, or logbooks.Collaborates in continuous improvement of laboratory operations.Supports NCMR and CAPA investigation when needed, supports audits when required.QualificationsQualificationsKnowledge, Skills and Abilities:Comprehend and apply written instructions, specifications, and methods in both English and Spanish.English intermediate level, read and write technical documents.Knowledge of GLP’s, GDP´s is a plus.Detail oriented, eager to learn, effective time management, adaptability to change, team working, proactive, and open to escalate concerns on time.Sitting for extended periods of time.Experience:0 to 2 years of previous experience in highly regulated industries such as medical device or pharmaceutical manufacturing in similar position.Experience with aseptic technique, manual, semi-automated, automated testing, and equipment is desirable.Education:Technical Degree in Microbiology laboratory or Chemical laboratory is required.Job InfoJob Identification 10062Job Category Clinical Life SciencePosting Date 03/30/2026, 09:32 PMJob Schedule Full timeJob Shift DayLocations Coyol Free Trade Zone, La Garita, Alajuela, CR (On-site)
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