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.
At Freudenberg Medical, we make products that save and improve the lives of people every day, all around the world. We are a global provider for medical device design and manufacturing with more than 2,500 employees. Innovation is at the core of our company, and we are proud of our industry-leading quality, lean manufacturing, and focus on innovation in products and processing technologies. Freudenberg Medical is an exciting place to work with lots of opportunity to learn, develop, and grow your career. Come join us and together we can make a difference in the future of healthcare.
Some of your Benefits
Diversity & Inclusion
Meal Allowance
On-site Medical Service
Personal Development
Public Transportation Allowance
Alajuela
On-Site
Freudenberg Medical srl.
You support our team as

• 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 Standards.
• Encourage the manufacturing associates and supporting staff to continually drive process improvements.
• Support all non-standard builds.
• Improve Quality. Focus on product, process, and paperwork quality by incorporating the following activities:
• Help 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