Your ‘day to day’:
ensure the timely execution of physical analyses in accordance with iso standards (including iso 17025) and guarantee product quality at the source through chromatography-based analytical analysis.
major accountabilities:
* perform tests and analyses on cigarettes following applicable procedures and analytical methods, with a focus on chromatography.
* ensure the integrity and timely reporting of analytical results in the designated systems.
* align with quality standards and maintain full adherence to the quality management system (qms).
* keep all procedures and formats aligned with iso 17025, iso 14001, and iso 45001 requirements up to date.
* participate in internal and external audits.
* contribute to safety and environmental objectives, encouraging a culture of sustainability across all pmi activities. Identify quality and safety deviations (qrp, bos, risk assessment, etc.) and take appropriate action.
* investigate non-conformities and deviations in a timely manner. Investigate critical deviations, define disposal actions, and support corrective actions when required.
* lead equipment verification, calibration, and maintenance according to schedule.
* propose and follow up on quality improvement initiatives within the laboratory or other operations processes.
* analyze information and participate in small-scale projects that influence product quality.
* provide support for special analyses and act as backup for other laboratories when needed.
who we’re looking for:
* bachelor’s degree in industrial engineering, chemical engineering, or a related field.
* 2–3 years of experience in quality, preferably with chromatography analysis within fmcg, pharmaceutical, or similar industries.
* advanced knowledge of iso 17025 and experience working in a certified laboratory.
* skills in priority setting, problem solving, and collaboration.
* fluent in spanish and intermediate level of english.