Inactive
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Smith+Nephew

Global medical devices for orthopedics

Manufacturing Engineer 1

Manufacturing EngineeringPosted on Nov 11
Full-timeAlajuela Province, Alajuela, Costa RicaNo salary listedIn-person

About the Job

Requirements

  • A Bachelor's degree in Mechanical, Electrical, Materials, Industrial, Electronics, Electromechanical, Mechatronics, Chemical, or Biotechnological Engineering is referred to in the education requirement.
  • Internal applicants must demonstrate experience in production or sustaining-related tasks at Smith & Nephew.
  • External applicants must have 0–1 year of Manufacturing Engineering experience; internships and university practicums count as relevant experience.
  • English proficiency at 60% conversational and 70% written is required.
  • Knowledge of Microsoft Office packages such as Word, Excel, and Outlook.
  • Ability to perform mathematical and statistical analysis and use sampling plans.
  • Knowledge of geometric dimensioning and tolerances.
  • Knowledge of Measurement System Analysis (MSA).
  • Ability to conduct validations (IQ/OQ/PQ/PPQ), create protocols, and support transfers.
  • Attention to detail and ability to solve problems and make decisions regarding components, documentation, and process changes during manufacturing batch production.
  • Ability to raise technical problems to the Engineering, Production, and Quality managers, R&D counterparts, and other support areas as required.
  • Ability to lift medium weights (5.1–30 kg), work 50% sitting and 50% standing, and perform repetitive computer use.

Responsibilities

  • Provide general, entry-level support to the engineering department on a daily basis or on assigned projects, verify and test assigned project metrics, and comply with Quality Systems requirements.
  • Comply with annual corporate objectives and contribute to established goals and financial results.
  • Prepare equipment, fixture, or basic-process validations (IQ/OQ/PQ/PPQ) to support correct implementation on the manufacturing line.
  • Identify and implement process improvements to stabilize processes, and coordinate with operational personnel to support tools and equipment.
  • Support production lines and their equipment, tools, and fixtures; address wear or failures that could increase scrap or delay product release, prepare necessary documents such as nonconformance investigations and rework instructions, and prioritize control and reduction of process variation.
  • Support issues involving components and raw materials used in final product assembly, resolving them promptly while minimizing production impact.
  • Support scrap reduction and first-pass yield improvement by identifying process improvements when products are transferred to the production line, reducing rework and component changes.
  • Work closely with the Quality Department on decisions related to specifications, raw materials, plans, and final products.
  • Create or revise documentation, including work instructions, routers, bills of materials, process FMEAs, engineering change notices, nonconformance reports, and laboratory notebooks.
  • Schedule meetings needed to complete projects and conduct engineering studies.
  • Improve or redesign fixtures.
  • Participate in the 5S program, statistical process control, or other company programs to improve productivity or processes.
  • Continuously improve yield, scrap, and first-pass quality levels in the assigned clean room.
  • Complete objectives or projects within the allotted period.
  • Work with departments across the corporation to facilitate internal and external information flow as required.
  • Understand and use basic SAP functions to obtain daily information.
  • Follow corporate induction, safety, quality, internal-policy, and other company requirements, and comply with the Quality Management System, including corrective and preventive action programs and quality standards, policies, and procedures.
  • Comply with occupational health standards and programs, use personal protective equipment, communicate safety improvements, and help prevent incidents or occupational diseases.
  • Safeguard documents, confidential information, equipment, tools, raw materials, products, and other work-area assets.
  • Train personnel on process changes when required.

Desired Qualifications

  • Knowledge of Good Manufacturing Practices (BPM), 5S, and Lean.
  • Knowledge of design software such as SolidWorks or equivalent.
  • Knowledge of Minitab or other statistical software.
  • Knowledge of Lean Manufacturing and creating value stream maps, including time-motion studies, waste measurement, balancing, and line standardization.

About the Company

Smith+Nephew

Global medical devices for orthopedics

Smith+Nephew is a global medical technology company that designs and makes medical devices for orthopaedics, sports medicine, and advanced wound care. Its products help surgeons treat joints and soft tissues and support patient recovery, including knee repair systems, single-use negative pressure wound therapy devices, and other extremity orthopaedic products. These devices are used in hospitals and clinics to perform procedures and support healing, often after surgery or injury. The company differentiates itself with a broad, worldwide product portfolio and collaborations with healthcare organizations to improve care and efficiency for patients and providers. Its goal is to improve patient outcomes, streamline medical procedures, and expand access to advanced medical solutions around the world.

Company size
10,001+
Company stage
IPO
Headquarters
Watford, United Kingdom
Founded
1856

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