2,804 Empleos en Puente de Piedra

Tasks and Responsibilities

Analyze current supply chain processes and identify opportunities for improvement.

Gather and document business requirements for supply chain systems and enhancements.

Collaborate with IT and business teams to design and implement system solutions.

Support the deployment and integration of ERP, WMS, TMS, and other supply chain platforms.

Conduct data analysis to support decision-making and performance monitoring.

Develop and maintain process documentation, workflows, and training materials.

Facilitate user acceptance testing and provide post-implementation support.

Ensure compliance with regulatory and internal standards across supply chain systems.

Manage relationships with vendors and service providers for supply chain technologies.

Support change management and training initiatives for new systems and processes.

Education and Experience

Bachelor's degree in Supply Chain Management, Information Systems, or related field.

5+ years of experience in supply chain systems analysis or business analysis.

Strong understanding of supply chain operations and technologies.

Experience with JDE E1 ERP system, WMS, TMS, and related platforms.

Project management certification (e.g., PMP, CAPM) preferred.

Experience in cross-functional collaboration and stakeholder engagement.

International experience and familiarity with global supply chain operations.

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at

Job Function
Project/Program Management Group

Job Sub Function
Project/Program Management

Job Category
Professional

All Job Posting Locations:
Grecia, Costa Rica

Job Description
Johnson & Johnson announced plans to separate our Orthopaedics business to establish a standalone orthopaedics company, operating as DePuy Synthes. The process of the planned separation is anticipated to be completed within 18 to 24 months, subject to legal requirements, including consultation with works councils and other employee representative bodies, as may be required, regulatory approvals and other customary conditions and approvals.

Should you accept this position, it is anticipated that, following conclusion of the transaction, you would be an employee of DePuy Synthes and your employment would be governed by DePuy Synthes employment processes, programs, policies, and benefit plans. In that case, details of any planned changes would be provided to you by DePuy Synthes at an appropriate time and subject to any necessary consultation processes.

Position Overview
The Senior Project Analyst / Scheduler will lead the implementation and management of the scheduling methodology, working closely with the various project workstream leaders, to ensure operational readiness in our newest manufacturing facility in Costa Rica.

We are recruiting for a Senior Project Scheduler – Project Epsilon
in our Network Transformation Team. This position will be located in Raynham, MA, Warsaw, IN, Cork, Ireland RT, Palm Beach Gardens, FL, or Grecia, Costa Rica.

Key Responsibilities

• Analyze and synthesize information from Project Team and external sources to develop integrated schedules.
• Perform qualitative analysis of project schedules to ensure Critical Path integrity and understand schedule constraints; work with teams to refine schedules, identify and suggest options, test "what-if" scenarios.
• Provide analysis and direction on estimated duration of scheduled tasks using standard process tools and techniques (analogous estimating, parametric estimating, reserve analysis, PERT).
• Run Risk Assessment and Monte Carlo Analysis and generation of corresponding reports.
• Validate optimized, agreed schedules against the overall project objectives.
• Evaluate project schedule progress and performance, monitoring project milestones and critical tasks.
• Identify developing schedule challenges with proactive troubleshooting of schedule issues.
• Maintain schedule change control process.
• Build targeted reports for coordination and schedule performance tracking purposes; develop custom reports - reporting the right information to the right partner at the right time.
• Lead resource loading of schedules to support project resource management requirements.
• Facilitate Interactive Planning sessions.
• Assist the project manager/PMO in running the project from a timeline perspective.
• Continuously evaluate and improve scheduling methodology and tools.

Experience And Education

• Experience of operating as a program scheduler in a sophisticated environment.
• Experience with schedule health metrics (e.g. DCMA 14-point check) and Schedule Metric Analysis.
• Proven levels of theoretical knowledge with practical application of planning & EV scheduling standards with a minimum of 1 years' experience in a senior scheduler role.
• A Bachelor's degree or equivalent experience in Project Management, Engineering, Science, Supply Chain/Operations, or related field.

Required Knowledge, Skills, Abilities, Certification/licenses

• Sophisticated proficiency in PPM & project scheduling software (MS Project Server).
• Microsoft Office, and advanced Excel abilities including pivot tables, macros, lookup tables.
• Proven understanding of Quality Management Standards.
• Good presentation skills.
• Concise and accurate, good with data.
• Critical thinking and problem solving.
• Confident and persuasive in briefings and meetings.

Preferred Skills

• PowerBI

Other
This position may require up to 10% domestic or international travel

Please note that this role is available across multiple countries and may be posted under different requisition numbers to align with local requirements. While you are welcome to apply to any or all of the postings, we recommend focusing on the specific country(s) that align with your preferred location(s):

US - Requisition Number:
R-
Ireland - Requisition Number:
R-
Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.

Location:
Grecia, Alajuela, Costa Rica

Meridia is seeking a meticulous and analytical Project Manager to manage and oversee financial aspects of a large program comprising multiple construction projects in the LIFESCIENCES sector. This role demands a high level of expertise in construction cost management, budget control, and financial reporting to ensure project alignment with budgetary goals and client financial objectives.

About the Role:
The successful candidate will be responsible for cost control processes, budget management, and financial oversight across all projects within the program. Responsibilities include coordinating with project managers, evaluating financial performance, performing cashflow variance analysis, developing and presenting budget relocations and implementing cost-saving measures.

Key Responsibilities:

Cost Management:

· Develop and maintain detailed project cost reports and forecasts.

· Monitor project budgets, actuals, commitments, and variances.

· Identify and analyze cost variances and recommend corrective actions.

· Ensure cost control procedures are followed and adhered to throughout the project lifecycle.

· Control cashflow compliance and assist the project management team on its development.

Budget Control:

· Prepare, review, and validate project budgets and cost estimates.

· Collaborate with project managers to establish cost control measures.

· Conduct regular budget reviews to ensure alignment with project milestones and deliverables.

Financial Reporting:

· Develop and explain financial reporting suitable for cross stakeholders and higher management.

Contract and Change Management:

· Review and validate suppliers' invoice amounts, backups documentation and timely delivery.

· Manage change order cycle, support PM on the change order presentation, ensure proper documentation of cost impacts and pursuit approval.

· Negotiate and resolve financial discrepancies with contractors and suppliers.

Risk Management:

· Identify financial risks and opportunities within the projects.

· Develop risk mitigation strategies and implement cost-saving initiatives.

· Conduct financial analysis to support risk management activities.

Qualifications:

· Bachelor's degree in Architecture, Civil engineering, Construction Engineering, or a related field.

· Minimum of 5 years of experience in cost control, budget management, or financial analysis in the construction industry, preferably in the free trade zone LIFESCIENCES sector.

· Proficiency in management software and Project Management platforms (e.g., Project Sight, Procore).

· Advanced skills in MS Excel and other financial analysis tools.

· Strong analytical and problem-solving abilities.

· Excellent communication and interpersonal skills.

· Preferred: Fluent in English (verbal and written).

· Teamwork abilities

· Professional appearance required

Nuestro cliente
Trelleborg Medical Solutions
, empresa líder en soluciones de ingeniería y manufactura de componentes médicos de precisión, iniciará operaciones en su nueva planta en Evolution Free Zone y busca
Operarios de Manufactura Nivel III (Senior)
para integrarse a su equipo de producción.

El puesto requiere personas con experiencia comprobada en manufactura médica, con capacidad para operar maquinaria avanzada y apoyar la coordinación de líneas de producción. Se valorará la formación técnica en
Buenas Prácticas de Manufactura (BPM/GMP)
o carreras afines, así como el dominio del inglés a nivel intermedio.

Responsabilidades:

• Operar y monitorear maquinaria de
  limpieza, inmersión, curado, mezclado y medición
  .
• Apoyar la
  coordinación de líneas o células de trabajo
  , asegurando la calidad del proceso y el cumplimiento de las metas.
• Ejecutar tareas de
  dipping y heat shrink
  , utilizando hornos, calibradores y selladoras.
• Garantizar el cumplimiento de normas de calidad, seguridad y eficiencia.
• Colaborar en el entrenamiento de nuevos operadores.

Requisitos:

• Título de secundaria completa (obligatorio).
• Técnico en BPM/GMP, Calidad o carrera afín (deseable).
• Experiencia mínima de tres a cinco años en manufactura médica
• Nivel de inglés intermedio, se requiere capacidad de comunicarse con el equipo en inglés.
• Experiencia en liderazgo operativo o coordinación de líneas.
• Conocimiento en el uso de
  instrumentos de medición, hornos y equipos automatizados
  .
• Conocimientos intermedios de computación.

Condiciones:

• Turno diurno.
• Salario competitivo
• Capacitación en sitio

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at

Job Function
Supply Chain Engineering

Job Sub Function
Manufacturing Engineering

Job Category
People Leader

All Job Posting Locations:
Grecia, Costa Rica

Job Description
About MedTech
Fueled by innovation at the intersection of biology and technology, we're developing the next generation of smarter, less invasive, more personalized treatments.

Your unique talents will help patients on their journey to wellness. Learn more at

About Orthopaedics
Fueled by innovation at the intersection of biology and technology, we're developing the next generation of smarter, less invasive, more personalized treatments.

Are you passionate about improving and expanding the possibilities of Orthopaedics? Ready to join a team that's reimagining how we heal? Our Orthopaedics teams help keep more than 6 million people moving each year while delivering clinical and economic value to surgeons and healthcare systems. Our teams build solutions for joint reconstruction; trauma and craniomaxillofacial; sports, extremities, and elective foot and ankle; spine; and robotics and digital surgery.

Your unique talents will help patients on their journey to wellness. Learn more at

We are searching for the best talent for Maintenance Supervisor.
Purpose
This role will execute engineering deliverables in support of large-scale manufacturing capacity projects that will yield stable, reliable and cost-effective manufacturing process meeting projects FPO's of capacity, product cost, budget and timeline.

The scope of this position will include both project delivery as well as ensuring knowledge transfer from developing manufacturing site staff and will work in collaboration with the existing DPS functional organizations to ensure standardization and the implementation of Best-in-Class practices.

This position supports the Orthopedics platform within J&J MedTech in manufacturing of orthopedic implants used in knee, hip and shoulder joint arthroplasty

You Will Be Responsible For
In accordance with all applicable federal, state and local laws/regulations and Corporate Johnson & Johnson, procedures and guidelines, this position:

• Supervises maintenance staff in execution of project deliverables
• Provides oversight of work, mentorship and coaching to maintenance staff to develop technical proficiency and assure delivery across the team
• Supporting delivery of robust and fully developed and qualified orthopaedic implant manufacturing processes to Network Edge projects
• Ensure that all project activities are conducted in line with procedures and controls outlined in the QMS and that the quality and performance of the product conforms to specified standards and in compliance with the recognized Regulatory Standards for relevant markets.
• Collaborate with functional stakeholders to ensure that technical, validation and regulatory strategies are implemented in an efficient and compliant manner and at an appropriate risk level
• Partner with Regulatory to execute the strategy necessary for all filings, inspections, and registrations in multiple sites and countries.
• Communicates with internal and external partners to coordinate and execute project plans.
• Provides technical leadership and supports execution of EHS&S policies and procedures
• Supporting technical collaboration across functions
• Leads effective and timely communication processes and stakeholder management processes within the project scope and ensures project and program activities are consistently documented.
• Responsible for communicating business related issues or opportunities to next management level
• Responsible for following all Company guidelines related to Health, Safety and Environmental practices as applicable.
• Responsible for ensuring personal and Company compliance with all Federal, State, local and Company regulations, policies, and procedures
• Performs other duties assigned as needed

Qualifications / Requirements
Experience and education

• University/Bachelors Degree or Equivalent
• Experienced knowledge of medical device manufacturing, maintenance and validation
• Minimum four (5) years of relevant professional work experience
• Ability to communicate effectively in English and Spanish across functions and both internally/externally
• Ability to perform duties in accordance with policies and procedures and in to comply civil rights requirements

Required Knowledge, Skills, Abilities, Certifications/licenses And Affiliations

• Asset Reliability expertise with PreventativePredictive maintenance
• Statistical and problem-solving engineering expertise (Six Sigma, SE or A3)
• Strong interpersonal and communication skills & demonstrated ability to operate as part of a team.
• Track record of innovation and adaptability in project execution, with strong problem-solving skills.
• Proven competence to evaluate communicate and act upon significant risks, demonstrating leadership of the high standards of quality and compliance.
• Strong influencing skills - Excellent interpersonal skills (written and oral).
• Decision Making – Required to make decisions on technical and management issues.
• Direct experience in manufacturing of high precision machined products within a highly regulated environment
• Experience with validation IQ/OQ/PQ and risk management documentation

Descripción de la empresa
Desarrollador Inmobiliario

Descripción del puesto
Generar experiencias de compra excepcionales mediante la asesoría especializada en la adquisición de lotes en condominio, combinando conocimiento técnico, herramientas digitales y habilidades comerciales para atraer, convertir y fidelizar a los clientes. Nuestros asesores inmobiliarios son responsables de gestionar todo el ciclo de ventas de forma profesional, eficiente y orientada al cumplimiento de metas comerciales.

Este es un puesto de tiempo completo y se realizará de manera presencial en nuestras oficinas ubicadas en Grecia.

Algunos Requisitos son:

• Habilidades interpersonales y de comunicación para interactuar eficazmente con los clientes.
• Experiencia en servicio al cliente y ventas para ofrecer una atención de calidad y cumplir con los objetivos de ventas.
• Capacidad para brindar formación tanto a clientes como a otros miembros del equipo cuando sea necesario.
• Se valorará experiencia previa en el sector inmobiliario y conocimiento del mercado local.
• Licencia de conducir B1, vehículo propio.

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at

Job Function
Supply Chain Engineering

Job Sub Function
Manufacturing Engineering

Job Category
People Leader

All Job Posting Locations:
Grecia, Costa Rica

Job Description
About MedTech
Fueled by innovation at the intersection of biology and technology, we're developing the next generation of smarter, less invasive, more personalized treatments.

Your unique talents will help patients on their journey to wellness. Learn more at

About Orthopaedics
Fueled by innovation at the intersection of biology and technology, we're developing the next generation of smarter, less invasive, more personalized treatments.

Are you passionate about improving and expanding the possibilities of Orthopaedics? Ready to join a team that's reimagining how we heal? Our Orthopaedics teams help keep more than 6 million people moving each year while delivering clinical and economic value to surgeons and healthcare systems. Our teams build solutions for joint reconstruction; trauma and craniomaxillofacial; sports, extremities, and elective foot and ankle; spine; and robotics and digital surgery.

Your unique talents will help patients on their journey to wellness. Learn more at

We are searching for the best talent for Engineering Team Lead.
Purpose

• This role will execute engineering deliverables in support of large-scale manufacturing capacity projects that will yield stable, reliable and cost-effective manufacturing process meeting projects FPO's of capacity, product cost, budget and timeline.
• The scope of this position will include both project delivery as well as ensuring knowledge transfer from developing manufacturing site staff and will work in collaboration with the existing DPS functional organizations to ensure standardization and the implementation of Best-in-Class practices.
• This position supports the Orthopedics platform within J&J MedTech in manufacturing of orthopedic implants used in knee, hip and shoulder joint arthroplasty.

You Will Be Responsible For
In accordance with all applicable federal, state and local laws/regulations and Corporate Johnson & Johnson, procedures and guidelines, this position:

• Supervises engineering staff in execution of project deliverables
• Provides oversight of work, mentorship and coaching to engineering staff to develop technical proficiency and assure delivery across the team
• Supporting delivery of robust and fully developed and qualified orthopaedic implant manufacturing processes to Network Edge projects
• Ensure that all project activities are conducted in line with procedures and controls outlined in the QMS and that the quality and performance of the product conforms to specified standards and in compliance with the recognized Regulatory Standards for relevant markets.
• Collaborate with functional stakeholders to ensure that technical, validation and regulatory strategies are implemented in an efficient and compliant manner and at an appropriate risk level
• Partner with Regulatory to execute the strategy necessary for all filings, inspections, and registrations in multiple sites and countries.
• Communicates with internal and external partners to coordinate and execute project plans.
• Provides technical leadership and supports execution of EHS&S policies and procedures
• Supporting technical collaboration across functions
• Leads effective and timely communication processes and stakeholder management processes within the project scope and ensures project and program activities are consistently documented.
• Responsible for communicating business related issues or opportunities to next management level
• Responsible for following all Company guidelines related to Health, Safety and Environmental practices as applicable.
• Responsible for ensuring personal and Company compliance with all Federal, State, local and Company regulations, policies, and procedures
• Performs other duties assigned as needed

Qualifications / Requirements
Experience and education

• University/Bachelors Degree or Equivalent
• Experienced knowledge of medical device manufacturing and validation
• Minimum four (5) years of relevant professional work experience
• Ability to communicate effectively in English and Spanish across functions and both internally/externally
• Ability to perform duties in accordance with policies and procedures and in to comply civil rights requirements

Required Knowledge, Skills, Abilities, Certifications/licenses And Affiliations

• Statistical and problem-solving engineering expertise (Six Sigma, SE or A3)
• Strong interpersonal and communication skills & demonstrated ability to operate as part of a team.
• Track record of innovation and adaptability in project execution, with strong problem-solving skills.
• Proven competence to evaluate communicate and act upon significant risks, demonstrating leadership of the high standards of quality and compliance.
• Strong influencing skills - Excellent interpersonal skills (written and oral).
• Decision Making – Required to make decisions on technical and management issues.
• Direct experience in manufacturing of high precision machined products within a highly regulated environment
• Experience with validation IQ/OQ/PQ and risk management documentation

Experiencia en diseños electromecánicos de al menos 3 años,

Manejo de CAD y Revit intermedio - avanzado, trabajos en la nube.

Conocimiento en materiales de construcción.

Interpretación de planos e información técnica de los mismos y detallado.

Conocimiento en la metodología BIM.

Para laborar en Grecia | Transporte gratuito desde San José y Heredia | Contratación inmediata.

Las personas interesadas enviar el CV al correo indicando el nombre del puesto y la pretensión salarial.

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at

Job Function
Quality

Job Sub Function
Quality Assurance

Job Category
Professional

All Job Posting Locations:
Grecia, Costa Rica

Job Description
About MedTech
Fueled by innovation at the intersection of biology and technology, we're developing the next generation of smarter, less invasive, more personalized treatments.

Your unique talents will help patients on their journey to wellness. Learn more at

We are searching for the best talent for Senior Metrology Engineer to be in Grecia, Costa Rica.
Purpose
The Senior Metrology Quality Engineer will be responsible for leading the definition of inspection requirements and qualification of inspection and test methods used in the manufacturing of orthopeadic implants and instruments.

You Will Be Responsible For
Under the direction of the Senior Quality Engineering Leader, and in accordance with all applicable federal, state and local laws/regulations and Corporate Johnson & Johnson, procedures and guidelines, this position:

• Interprets drawings featuring Geometric Dimensioning & Tolerancing (GD&T) per ASME Y14.5 to identify product inspection requirements.
• Identify product inspection requirements.
• Serves as technical expert for metrology inspection.
• Facilitates, encourage and coordinate continuous improvement with respect to inspection activities.
• Coordinate data collection parameters for inspection measurements where required.
• Provides guidance on installation of inspection assets as to ensure compliance to procedures.
• Develops inspection strategies to meet business needs.
• Development of standard platforms where applicable (vision systems, contact/noncontact inspection systems.
• Develop method of "gauge" evaluation to consider, calibration frequencies, gauge life, fit for purpose, etc.
• Lead on development of inspection fixturing to ensure minimum measurement error during inspection.
• Participates in reviews on cross-functional teams to ensure that conformance to specifications, inspect ability, reliability, and quality system objectives are met.
• Assist engineers with qualification and validation of new or changed tooling or parts.
• Work from written or verbal instructions, detailed engineering drawings, and 3D models.
• Writing of work instructions for qualification of inspection techniques relating to standard platforms.
• Input into validation approach in conjunction for all inspection platforms.

Qualifications / Requirements

• A minimum of a high school diploma. Bachelor's Degree in engineering: Mechanical, Electrical, Industrial or applicable science is preferred.
• 4 years experience as a Quality Professional in the Medical Device Industry required.
• Demonstrated knowledge of manufacturing and inspection principles and practices, and procedures

Skills

• Experience in selection and procurement of inspection equipment
• Proficient in writing and editing CMM programs (PC-DMIS/COSMO/CALYPSO)
• Proficient in set-up and operation of inspection equipment
• Proficient in metrology methods/technology
• Proficient in reading/interpreting engineering drawings and the application of Geometric Dimensioning & Tolerancing (GD&T) per ASME Y14.5
• Proficient in mathematical applications - Algebra, Geometry, & Trigonometry
• Proficient in Microsoft Word & Excel.
• Excellent interpersonal & communication skills
• Knowledge of mechanical inspection methods and tools used to determine product acceptance
• Ability to investigate and learn new technologies in metrology

Preferred

• Minimum 3 years in CMM programming PC-DMIS / COSMOS / CALYPSO programming experience
• Experience with laser scanning techniques and other inspection technologies.
• Familiarity with statistical analysis software (i.e. Minitab)
• Knowledge of 21 CFR 820, 21 CFR 11 and European regulations associated with the medical device industry
• Working knowledge of GMP and Quality Systems (FDA/ISO) within a regulated environment.
• Certifications such as CQA, CQE, CQM (preferably), CBA, MBB or BB are a plus