Manufacturing Engineer I (Alajuela, Costa Rica)

Costa RicaHybrid

Responsibilities

Create, modify, and maintain technical documentation and design records within a data management (PDM/PLM) environment, ensuring version control and traceability.
Collaborate with cross-functional partners (R&D, engineering and quality) to ensure CAD models and drawings meet project requirements and timelines.
Ensure all CAD updates are executed in accordance with approved ECOs and flow through drawings, BOMs, and PLM records.
Design Documentation: Maintain Design History Files (DHF) and ensure CAD drawings accurately reflect released product configurations.
Support incorporation of supplier and manufacturing feedback into drawings under engineering guidance BOM Management: Support the creation and maintenance of Bills of Materials (BOM) in ERP systems.

The Engineer I will provide dedicated SolidWorks CAD modeling and drafting support for new product development and sustaining engineering teams.
This position executes CAD and documentation tasks under the direction of Engineers and does not hold independent design authority.
This role builds foundational medical‑device CAD, documentation, and change‑control skills, with potential progression into Design Engineering, Manufacturing Engineering, or Product Development roles.
This position is a P1 level (internal use) What will you be doing? CAD Management: Create, update, and manage 3D CAD models and detailed 2D drawings using SolidWorks .
Legacy Data Conversion: Convert older CAD files (PDFs, DXF) into modern, functional SolidWorks part and assembly files.
What will you need to be successful? Education : Bachelors Degree in Mechanical Engineering Licenses/ Certifications : SolidWorks CSWA or equivalent certification preferred.
Experience: SolidWorks Proficiency: 1-3 years of professional
Technical Knowledge: Basic understanding of GD&T, engineering drawings, and manufacturing processes (e.g., plastic injection molding, machining).
Documentation Tools: Familiarity with PDM/PLM systems (e.g., SolidWorks PDM, Windchill).
Language : Advanced English level Competences:
Experience in the medical device industry (knowledge of ISO 13485, FDA 21 CFR 820).
Experience with ERP systems. Physical Demands: ability to lift 25lbs on an occasional basis Travel

Learn more about our Employee Inclusion Groups on our website https://www.smith-nephew.com/ Your future: stock purchase program, referral bonus, subsidy in transport and food, recognition program.
Work/Life Balance: Extra days off, birthday off, voluntary hours.
Your Wellbeing: company doctor, medical insurance, gym, health campaigns, employee assistance program, parental leave.
Extra perks: employees association, and more… #LI-HYBRID Stay connected by joining our Talent Community .

At Smith+Nephew we design and manufacture technology that takes the limits off living.
Engineering Changes (ECOs): Process and implement redlines, markups, and engineering change orders (ECO) to update designs and documentation.
Drafting Standards: Ensure all drawings adhere to GD&T (Geometric Dimensioning and Tolerancing) standards and internal company templates.
Collaboration: Work with engineering, manufacturing, and quality teams to ensure design changes are manufacturable and meet quality requirements.
experience (or intensive internship experience) utilizing SolidWorks in a drafting or design support role.
Attention to Detail: Meticulous approach to documentation to ensure precision in a regulated environment.
Unlimited We believe in creating the greatest good for society.
Our strongest investments are in our people and the patients we serve.
Inclusion + Belonging - Committed to Welcoming, Celebrating and Thriving.
Flexibility : Hybrid work model (for more professional roles), flexible schedules.