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Team Lead Shift C jobs at Boston Scientific in Costa Rica, El Amparo

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Costa Rica
El Amparo
6 jobs found
17.05.2025
BS

Boston Scientific Quality Engineer Shift B Costa Rica, Alajuela Province, El Amparo

Limitless High-tech career opportunities - Expoint
Identify Manufacturing process defects (scrap, nonconforming material, customer complaints) by dispositioning non-conforming material, assisting in identification of primary root causes and understanding corrective and preventative actions. May be responsible for...
Description:

Costa Rica-Coyol

Hybrid Roles:

Your responsibilities include:

  • Identify Manufacturing process defects (scrap, nonconforming material, customer complaints) by dispositioning non-conforming material, assisting in identification of primary root causes and understanding corrective and preventative actions. May be responsible for working with process owner to bound product stops and document release criteria.
  • Understanding of product quality plans, documents and systems by reviewing product specifications, quality specifications, and working with quality systems. May be responsible for learning risk analyses and FMEAs.
  • Monitoring Systems by becoming familiar with systems applications and critical process steps; and through familiarization with methods used to reduce process variation.
  • Becomes familiar with Product/Process improvement efforts by understanding current quality metric data and learning the various analysis methods used to enhance sustaining product design and new product development
  • Learns Quality Tools & Training Materials by gaining knowledge of prevalent tools used and by reviewing & utilizing available training materials.
  • Checks and provides support in the execution and investigation of CAPAs, NCEP, Failure Mode Investigations, etc.
  • Evaluates new equipment and processes and participates in the transfer of new products.
  • Get involve in various stages of equipment and processes validations: Run and / or review and / or approve reports I.Q 's, O.Q' s and P.Q 's as well as any other document relating to validation.
  • Read and interpret technical drawings, procedures, and protocols
  • Assure that all laboratory equipment is in compliance to perform the analysis activities (calibration, safety, cleanness).
  • Document investigation findings in analysis report on GCS2
  • Become a trainer for the Software related with complaints handling process (GCS2), as required.
  • Work with Research and Development to efficiently qualify new components; assist suppliers in creating of statistical sampling plans, inspection methodology and quality procedures for new components
  • Responsible for reviewing and developing process validation protocols and reports. Support other functional areas during the validation activities
  • Support environmental monitoring, microbiology and product testing as in approved procedures and protocols.

Required Qualifications:

  • Bachelor's degree in Chemical, Industrial, Electronic, Biotechnology, Electromechanical Engineering or Related Field
  • 0+ years of related work experience or an equivalent combination of education and work experience
  • English language required B2: 70-79

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16.05.2025
BS

Boston Scientific Production Supervisor II Shift B Coyol Costa Rica, Alajuela Province, El Amparo

Limitless High-tech career opportunities - Expoint
Oversee operations efficiency and standardization. Directly responsible for complying with the production plan and the quality of the product, as well as for line personnel. Analyze and evaluate process improvements...
Description:

Costa Rica-Coyol

About the role:

Responsible for the efficient management of production resources: equipment, personnel and materials.

Your Responsibilities Include:

  • Oversee operations efficiency and standardization.
  • Directly responsible for complying with the production plan and the quality of the product, as well as for line personnel.
  • Analyze and evaluate process improvements in order to reduce defects and scrap and/or improving yields.
  • Follow procedures established for each operation, and keep work areas organized and clean at all times.
  • Participate and/or lead problem solving processes, whether due to increasing trends on complaints, defects, scrap, or low productivity, among others.
  • Provide feedback to PB IV.
  • Support employee-safety oriented initiatives: rotation programs of line personnel, use of safety equipment in the production area, and EH&S awareness programs.
  • Support EHS management system: responsible of understand, know and apply EHS policy. Responsible to acknowledge and inform the environmental aspects and health and safety risks relevant to mitigate, reduce and eliminate impact during operations.
  • Monitor and update the department´s metrics: Yield, Efficiency, Plan Compliance, RCTIME and Quality.

What we're looking for:

  • Bachelor or Licenciature degree in Business Administration, Industrial Engineering or Related Field.
  • English Level desired: 70-79%
  • Experience: At least 2 years
  • Technical Competencies: Problem Solving Methodologies.
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These jobs might be a good fit

07.05.2025
BS

Boston Scientific Engineer II QA - Shift C Costa Rica, Alajuela Province, El Amparo

Limitless High-tech career opportunities - Expoint
May execute the following resposibilities:Identify Manufacturing process defects (scrap, nonconforming material, customer complaints) by dispositioning non-conforming material, assisting in identification of primary root causes and understanding corrective and preventative actions....
Description:

Hybrid Roles:

You're Responsibilities include:

  • May execute the following resposibilities:Identify Manufacturing process defects (scrap, nonconforming material, customer complaints) by dispositioning non-conforming material, assisting in identification of primary root causes and understanding corrective and preventative actions. May be responsible for working with process owner to bound product stops and document release criteria.
  • Understanding of product quality plans, documents and systems by reviewing product specifications, quality specifications, and working with quality systems. May be responsible for learning risk analyses and FMEAs.
  • Monitoring Systems by becoming familiar with systems applications and critical process steps; and through familiarization with methods used to reduce process variation.
  • Becomes familiar with Product/Process improvement efforts by understanding current quality metric data and learning the various analysis methods used to enhance sustaining product design and new product development
  • Learns Quality Tools & Training Materials by gaining knowledge of prevalent tools used and by reviewing & utilizing available training materials.
  • Checks and provides support in the execution and investigation of CAPAs, NCEP, Failure Mode Investigations, etc.
  • Evaluates new equipment and processes and participates in the transfer of new products.
  • Get involve in various stages of equipment and processes validations: Run and / or review and / or approve reports I.Q 's, O.Q' s and P.Q 's as well as any other document relating to validation.
  • Read and interpret technical drawings, procedures, and protocols
  • Assure that all laboratory equipment is in compliance to perform the analysis activities (calibration, safety, cleanness).
  • Document investigation findings in analysis report on GCS2
  • Become a trainer for the Software related with complaints handling process (GCS2), as required.
  • Work with Research and Development to efficiently qualify new components; assist suppliers in creating of statistical sampling plans, inspection methodology and quality procedures for new components
  • Responsible for reviewing and developing process validation protocols and reports. Support other functional areas during the validation activities
  • Provide supervision, leadership, and overall direction to the Quality Release team to ensure they are identifying issues, quarantining defective product, and efficiently moving product through the release process. Clarify priorities and remove roadblocks to maintain a high level of quality in accordance with ISO standards, cGMP's, Corporate and site level SOP's.

What We’re Looking For:

  • Bachelor's degree in Industrial Engineering, Quimical Engineering, Electrical Engineering, Electronic Engineering or any similar
  • English Level desired: B2+
  • Experience: 2+ years
  • Or an equivalent combination of education and experience.
  • Desired knowledge: ISO485, Power BI, SAP, MES, Minitab, Non conformance handling

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These jobs might be a good fit

03.05.2025
BS

Boston Scientific Team Lead Shift C Costa Rica, Alajuela Province, El Amparo

Limitless High-tech career opportunities - Expoint
Oversee operations efficiency and standardization. Directly responsible for complying with the production plan and the quality of the product, as well as for line personnel. Analyze and evaluate process improvements...
Description:

Costa Rica-Coyol

About the role

Responsible for the efficient management of production resources: equipment, personnel and materials. This position will work on Shift C (Turno C) Sunday to Friday, from 10pm to 6am.

Job responsibilities include:

  • Oversee operations efficiency and standardization.
  • Directly responsible for complying with the production plan and the quality of the product, as well as for line personnel.
  • Analyze and evaluate process improvements in order to reduce defects and scrap and/or improving yields.
  • Follow procedures established for each operation, and keep work areas organized and clean at all times.
  • Participate and/or lead problem solving processes, whether due to increasing trends on complaints, defects, scrap, or low productivity, among others.
  • Provide feedback to PB IV.
  • Support employee-safety oriented initiatives: rotation programs of line personnel, use of safety equipment in the production area, and EH&S awareness programs.
  • Support EHS management system: responsible of understand, know and apply EHS policy. Responsible to acknowledge and inform the environmental aspects and health and safety risks relevant to mitigate, reduce and eliminate impact during operations.
  • Monitor and update the department´s metrics: Yield, Efficiency, Plan Compliance, RCTIME and Quality.

Minimum Requirements:

  • Bachelor’s degree or above in Industrial Engineering (GRADUATED)
  • 2+ years of related work experience
  • Advanced English level (B2/70-79%)
  • Experience managing people
  • Experience in medical industry
Show more

These jobs might be a good fit

25.04.2025
BS

Boston Scientific Production Supervisor II Shift Coyol Costa Rica, Alajuela Province, El Amparo

Limitless High-tech career opportunities - Expoint
Oversee operations efficiency and standardization. Directly responsible for complying with the production plan and the quality of the product, as well as for line personnel. Analyze and evaluate process improvements...
Description:

Costa Rica-Coyol

Hybrid Roles:

About the role:

Responsible for the efficient management of production resources: equipment, personnel and materials.

Your Responsibilities Include:

  • Oversee operations efficiency and standardization.
  • Directly responsible for complying with the production plan and the quality of the product, as well as for line personnel.
  • Analyze and evaluate process improvements in order to reduce defects and scrap and/or improving yields.
  • Follow procedures established for each operation, and keep work areas organized and clean at all times.
  • Participate and/or lead problem solving processes, whether due to increasing trends on complaints, defects, scrap, or low productivity, among others.
  • Provide feedback to PB IV.
  • Support employee-safety oriented initiatives: rotation programs of line personnel, use of safety equipment in the production area, and EH&S awareness programs.
  • Support EHS management system: responsible of understand, know and apply EHS policy. Responsible to acknowledge and inform the environmental aspects and health and safety risks relevant to mitigate, reduce and eliminate impact during operations.
  • Monitor and update the department´s metrics: Yield, Efficiency, Plan Compliance, RCTIME and Quality.

What we're looking for:

  • Bachelor or Licenciature degree in Business Administration, Industrial Engineering or Related Field.
  • English Level desired: 70-79%
  • Technical Competencies: Problem Solving Methodologies.

Show more

These jobs might be a good fit

18.04.2025
BS

Boston Scientific Team Lead Turno B Costa Rica, Alajuela Province, El Amparo

Limitless High-tech career opportunities - Expoint
Oversee operations efficiency and standardization. Directly responsible for complying with the production plan and the quality of the product, as well as for line personnel. Analyze and evaluate process improvements...
Description:

Costa Rica-Coyol

About the role

Responsible for the efficient management of production resources: equipment, personnel and materials. This position will work on Shift B (Turno B).

Job responsibilities include:

  • Oversee operations efficiency and standardization.
  • Directly responsible for complying with the production plan and the quality of the product, as well as for line personnel.
  • Analyze and evaluate process improvements in order to reduce defects and scrap and/or improving yields.
  • Follow procedures established for each operation, and keep work areas organized and clean at all times.
  • Participate and/or lead problem solving processes, whether due to increasing trends on complaints, defects, scrap, or low productivity, among others.
  • Provide feedback to PB IV.
  • Support employee-safety oriented initiatives: rotation programs of line personnel, use of safety equipment in the production area, and EH&S awareness programs.
  • Support EHS management system: responsible of understand, know and apply EHS policy. Responsible to acknowledge and inform the environmental aspects and health and safety risks relevant to mitigate, reduce and eliminate impact during operations.
  • Monitor and update the department´s metrics: Yield, Efficiency, Plan Compliance, RCTIME and Quality.

Minimum Requirements:

  • Bachelor’s degree or above in Industrial Engineering (GRADUATED)
  • 2+ years of related work experience
  • Advanced English level (B2/70-79%)
  • Experience managing people
  • Experience in medical industry

Show more

These jobs might be a good fit

Limitless High-tech career opportunities - Expoint
Identify Manufacturing process defects (scrap, nonconforming material, customer complaints) by dispositioning non-conforming material, assisting in identification of primary root causes and understanding corrective and preventative actions. May be responsible for...
Description:

Costa Rica-Coyol

Hybrid Roles:

Your responsibilities include:

  • Identify Manufacturing process defects (scrap, nonconforming material, customer complaints) by dispositioning non-conforming material, assisting in identification of primary root causes and understanding corrective and preventative actions. May be responsible for working with process owner to bound product stops and document release criteria.
  • Understanding of product quality plans, documents and systems by reviewing product specifications, quality specifications, and working with quality systems. May be responsible for learning risk analyses and FMEAs.
  • Monitoring Systems by becoming familiar with systems applications and critical process steps; and through familiarization with methods used to reduce process variation.
  • Becomes familiar with Product/Process improvement efforts by understanding current quality metric data and learning the various analysis methods used to enhance sustaining product design and new product development
  • Learns Quality Tools & Training Materials by gaining knowledge of prevalent tools used and by reviewing & utilizing available training materials.
  • Checks and provides support in the execution and investigation of CAPAs, NCEP, Failure Mode Investigations, etc.
  • Evaluates new equipment and processes and participates in the transfer of new products.
  • Get involve in various stages of equipment and processes validations: Run and / or review and / or approve reports I.Q 's, O.Q' s and P.Q 's as well as any other document relating to validation.
  • Read and interpret technical drawings, procedures, and protocols
  • Assure that all laboratory equipment is in compliance to perform the analysis activities (calibration, safety, cleanness).
  • Document investigation findings in analysis report on GCS2
  • Become a trainer for the Software related with complaints handling process (GCS2), as required.
  • Work with Research and Development to efficiently qualify new components; assist suppliers in creating of statistical sampling plans, inspection methodology and quality procedures for new components
  • Responsible for reviewing and developing process validation protocols and reports. Support other functional areas during the validation activities
  • Support environmental monitoring, microbiology and product testing as in approved procedures and protocols.

Required Qualifications:

  • Bachelor's degree in Chemical, Industrial, Electronic, Biotechnology, Electromechanical Engineering or Related Field
  • 0+ years of related work experience or an equivalent combination of education and work experience
  • English language required B2: 70-79

Show more
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