Job Opportunities in Costa Rica

Functional Job Family Description
This position will provide engineering support to production through improvement or implementation of methods, processes, fixtures and tools. Additionally, you will propose and/or execute electro-mechanical improvements that result in improved cycle times. Responsibilities include, but are not limited to, validation, maintenance and introduction of new equipment and processes, including supporting documentation within an ISO 13485 environment. Develop training tools that facilitate compliance with Creganna Medical Standard Operating Procedures (SOP).


Nature and Overall Purpose of the Role
Responsibility Includes the Following Tasks

• Learn, apply and share knowledge of products, manufacturing processes and equipment.

• Lead or participate in projects to maximize productivity.

• Lead or participate in cost reduction projects, such as: scrap reduction, flow improvement, inventory reduction, cycle time reduction, etc.

• Monitor manufacturing process activities, measure important process characteristics and analyze variation in order to detect and reduce waste.

• Analyze and provide information for decision making related to the outcome of key indicators for the manufacturing process.

• Lead or participate in the introduction of new part numbers into an existing technology platform or process.

• Lead process and equipment validations (IQ, OQ, PQ).

• Sourcing and implementing new technologies that maximize the operation. E.g.Obsolescence, increased capacity, versatility, ergonomics, etc.

• Participate in the activities of multidisciplinary teams for the solution of problems related to product quality (NCMR’s, CARS, SCARS, CAPA's, etc.)

• All other functions with respect to the manufacturing process.

What your background should look like:

COMPETENCIES & SKILLS

• Ethics and Values- Commitment with quality and effectiveness.

Skills- Completion of improvement projects according to the defined date.
Abilities

• Ability to Work under pressure.

• Ease of adapting to change.
• Closing of CAPA's, NCMR's on the assigned date.

• Search for continuous improvement.

• Validation Compliance.

EXPERIENCE & EDUCATIONAL REQUIREMENTS
Experience

• 3 to 6 years of work experience.years of experience.

• Previous experience in the medical industry is preferred

• Knowledge of FDA and/or ISO 13485 preferred.

• Knowledge of Solidworks,CAD Minitab.

• Preferred knowledge in Lean Manufacturing, Six Sigma, Quality,etc.

• 80% English proficiency.

Education

• Bachelor's degree in Industrial, Mechanical, Electromechanical

Engineering, or any other engineering related to the position.

Competencies