Do you have a passion for helping launch and manufacture innovative medical and drug delivery devices that can help improve lives?
We are growing and looking for a Design Transfer Engineer to help create innovative solutions for patients and customers by managing technical risks and ensuring high-quality outcomes, Gilero, A Sanner Company, partners with Tecma to operate a medical device manufacturing facility in Tijuana, Mexico.
We are currently seeking a Design Transfer Engineer to join the TJ team!
Design Transfer Engineers draw on experience to bridge product development and manufacturing, taking a medical device from late-stage development through manufacturing readiness and commercial launch.
They coordinate technical, quality, operational, and project activities to ensure the product can be manufactured consistently, compliantly, and at the required scale.
In this position you will champion teamwork and ensure seamless collaboration with customers, vendors, and internal teams.
ResponsibilitiesCollaborate with the product development and manufacturing team to identify and mitigate risks prior to commercial launchPrepare programs for pilot/development GMP builds for design verification, clinical trials, etc.Manage product development deliverables through the entire development lifecycle, with a focus on manufacturing transferSupport sustaining engineering activities for products in commercial manufacturingWrite and execute protocols to assess manufacturing process capability (IQ/OQ/PQ)Maintain and develop Device Master Record (DMR) and ensure documents are complete, accurate, and current including process routers, inspection plans, temporary deviations, and nonconformancesParticipate in manufacturing investigations/CAPA resolutions to identify improvements to the manufacturing processesFacilitate design transfer of existing products to and from other manufacturing sitesTrack technical risk and provide engineering guidanceSeek feedback and mentorship from senior engineersHelp lead the development team through technical risk retirement.




Support the team on technical risks through step-by-step simplification to discover root causeManage product development deliverables through the entire development lifecycle, with a focus on manufacturing transferCreate, review, and release documents according to Gilero's QMS and the lifecycle of the project and develop test methods and protocols to fulfill state of the art requirementsKeep project managers informed on technical projects variables and statusPrepare documentation to support design history files and regulatory submissionsAnalyze test data, interpret results, formulate conclusions, and apply statistical techniques (t-test, ANOVA, UCL/LCL, Tolerance Intervals)Support delivery of project objectives and milestonesParticipate in testing campaigns, test flows, sample size analysis, and justification, based on sound judgment, Risk analysis, and QMS requirementsSupport product and process risk assessments, including hazard analysis, FMEAs and residual risk analysis in conjunction with Quality EngineeringSupport test method development and validationOversee and perform testing and inspection of prototypes and pre-production products including assisting assembly for DV&V; builds and clinical buildsSupport investigation of device failures, coordinate resources, determine root cause, identify corrective actions, and document in conjunction with Quality EngineeringSkills/Qualifications:BS in Engineering or equivalent technical degreeMinimum 3 years' experience in medical device manufacturing.
Skilled at transforming technical situations into well-defined project deliverablesUnderstanding of good GMP and GDPUnderstanding of the Phase Gate SystemExposure and understanding of ISO *****,



***** and CFR 21 Knowledge baseAbility to translate User Needs/Requirements into measurable technical/product requirements and set appropriate specification though thought experiments and empirical testingAbility to support and document appropriate scenarios for rationale-based decisions versus testing-based approachesAbility to author scientific/logic-based rationaleAwareness of pre-clinical validation and GLPAbility to review and understand technical drawings and GD&T; to support development lifecycleAbility to review, understand, and distill technical standards (ISO, ASTM, IEC, etc)Excellent communication skills (oral and written).
Proficient in conversational English.Personal Attributes:Meets Gilero Core Values of Collaboration - embracing teamwork and transparency in our organization, partnering with our customers and vendors; Integrity - doing the right thing at all times; fair and trustworthy; always keeping the patient in mind; Innovation - open to new ideas, processes, and solutions; leveraging technology to creatively solve problems and Excellence - delivering exceptional products and services with passion and pride.Comfortable and productive in a fast-paced, entrepreneurial environmentA self-starter seeking a career opportunity with potential for internal advancement, seekingCommitment to excellence and quality service to external and internal customersFollow established policies and procedures, while contributing to continuous improvementsWhy work at Gilero?
Founded in ****, Gilero, a Sanner Group company, is an international contract engineering firm that specializes in the design, development, and manufacturing of novel medical devices and drug delivery products.
At Gilero we are proud of the culture we have built that directly reflects our values of excellence, integrity, innovation, and collaboration.
Motivated by our purpose to benefit people and improve patient outcomes, our team continue to grow at a rapid pace.
Locations include Tijuana, Mexico and US locations in Carlsbad, CA; Chicago, IL; as well as NC locations in Raleigh, Durham, Greensboro, and Pittsboro.

📌 Design Transfer Engineer - Medical Device Industry (Tijuana)
🏢 Gilero, A Sanner Group
📍 Tijuana