Job Description

Working at Freudenberg: "We will wow your world!" This is our promise. As a global technology group, we not only make the world cleaner, healthier and more comfortable, but also offer our 52,000 employees a networked and diverse environment where everyone can thrive individually. Be surprised and experience your own wow moments.Freudenberg Medical is a trusted Contract Manufacturing Organization (CDMO) partner, delivering high-quality solutions from ideation and market launch to volume production for medical device and pharmaceutical companies. With proven expertise in materials and technologies, Freudenberg Medical offers an extensive range of vertically integrated capabilities: precision molding and extrusions, complex catheters, hypotubes, and coatings.Some of your Benefits Cafeteria/ Canteen: We offer fresh food on-site, both hot and cold.On-site Medical Service: Our on-site medical service can handle a variety of medical needs.Diversity & Inclusion: We focus on providing an inclusive environment and recognize our diversity contributes to our success.Public Transportation Allowance: Commute more affordable thanks to public transport allowance.Meal Allowance: We offer an allowance that makes meals more affordable. AlajuelaOn-Site Freudenberg Medical srl.You support our team as Engineering Techician Responsibilities Responsible of creation, documentation of the Validation Protocols (Engineering studies, IQ, OQ, PQ).Perform packaging simulations and validation runs and lots in the respective line/area.Complete and processing of the validation final report (IQ, OQ, PQ).Formulation and Execution of Engineering Test (documentation, justification, conclusion and final report).Perform the configuration in the ERP System of each part number (Material Master, BOM and Recipe).Support to manufacturing in the maintenance and data accuracy the information of each part number in the ERP System (Material Master, BOM and Recipe).Perform the measurement of quality characteristics of the engineering samples, FAI and Validation samples.Perform data analysis using statistics tool (Capability Analysis, Control Charts, hypothesis test, descriptive statistics, MSA, DOE, tec.)Support the Manufacturing Engineer’s efforts in Product and Process Development.Support the Manufacturing Engineer’s in the controls of products and process during post validation and lunch of process/product to manufacture.Support to engineering complete the equipment initiation form and determine the calibration information.Support the new equipment installation in the plant.Responsible for the identification and storage of the engineering samples into the clean room and around to the plant.Support the Manufacturing Engineer in the creation, release and information maintenance of the UT and OP equipment documents.Support the Manufacturing Engineer in the creation of WI, MP, SOP, FORM and Manufacturing StandardsEncourage the manufacturing associates and supporting staff to continually drive process improvements.Support all non-standard builds.Contribute to improved resource efficiency by conserving energy, water, and materials where possible,Contribute to the continual improvement of HSE systems by actively participatingHelp the Manufacturing Engineer to ensure process improvements are implemented to increase product quality.Support the Manufacturing Engineer’s work with the Quality Engineer towards identification of root causes of manufacturing issues. If a QN is issued, support the efforts to ensure the item is closed in an appropriate amount of time.Support the Quality Engineer(s) presentation of customer complaint data and actions to the production line associates.Performs other duties as assigned including working on the line as needed and supporting the environmental program technician by taking particulate counts and other activities.Qualifications Technician degree in electromechanical, mechanical, electric, electronics, molding or similar.Experience in the lines and area assigned is a plus.Technical degree.Must spend the majority of the working day in the controlled environmentInvolves sitting, standing and/or walking.Capable to follow written and verbal instructionsHe/She must have good manual dexterity.Accurate and attention to detailsAbility to problems resolution.High gift of service and responsibility to others, high ethical and moral values.Numerical Ability and ObservationThe Freudenberg Group is an equal opportunity employer that is committed to diversity and inclusion. Employment opportunities are available to all applicants and associates without regard to race, color, religion, creed, gender (including pregnancy, childbirth, breastfeeding, or related medical conditions), gender identity or expression, national origin, ancestry, age, mental or physical disability, genetic information, marital status, familial status, sexual orientation, protected military or veteran status, or any other characteristic protected by applicable law.

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