דרושים Engineer Sr Equipment ב-Boston Scientific ב-קוסטה ריקה

Costa Rica-Heredia

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

What we're looking for:

• Bachelor or Licenciature degree in Chemical, Industrial, Electronic, Biotechnology, Electromechanical Engineering or Related Field.
• Experience: At least 5 years
• English Level desired: 70-79%
• Technical Competencies: ASQ Certified, Problem Solving, Networking

Benefits • Life-Work Integration • Community • Career Growth

Costa Rica-Heredia

Hybrid Roles:

About the role:

This is a hybrid position based out of Heredia, Costa Rica with the expectation to be in the office a minimum of three days per week.

Your responsibilities include:

• Support the execution and documentation of Design Validation & Verification and Usability activities.
• Apply sound, systematic problem-solving methodologies in identifying, prioritizing, communicating, and resolving quality issues.
• Work within a cross-functional team to identify and implement effective controls and support product development from concept through commercialization.
• Update and maintain product risk management tools (i.e. Hazard Analysis, Fault Tree, FMEAs).
• Working knowledge of Design Controls. Provide quality and compliance input to project teams for project decisions and deliverables (i.e., Design Change Analysis, Design Inputs, Design Outputs, Test Methods, Design Reviews, Design V&V, Usability Testing, Process Validation and Labeling).
• Lead and support cross-functional root-cause analysis investigation and resolution activities.
• Checks and provides support in the execution and investigation of CAPAs, NCEP, Failure Mode Investigations, etc.
• Reviews and approves operational, test and validation data to establish technical specifications and performance standards for newly designed or modified products and processes.
• Support regulatory submissions to notified bodies.
• Demonstrates a primary commitment to patient safety and product quality by maintaining compliance to the Quality Policy and all other documented quality processes and procedure.

What we’re looking for:

Required Qualifications:

• Bachelor’s degree in mechanical engineering, Biomedical Engineering or related field of study
• 5+ years of experience in design assurance, quality, new product development, or related medical device / regulated industry experience
• Detailed understanding of US and International regulations including 21 CFR, 820, 210, 211, and 11 is required, as well as the Medical Device Directive, EN ISO 13485, and EN ISO 14971.
• High energy problem solver capable of driving items to closure.
• Adaptable and effective collaborator in a team environment and in self-directed work
• Strong communication skills (verbal & written)

Preferred Qualifications

• Demonstrated use of Quality tools/methodologies

Benefits • Life-Work Integration • Community • Career Growth

• Design & Develop Automations: Build and deploy automation workflows using Power Platform and RPA technologies to streamline operations, reduce manual effort, and improve accuracy.
• Business Process Understanding: Collaborate with functional stakeholders to map, analyze, and document business processes, ensuring automation aligns with organizational needs.
• Critical Thinking & Solution Alignment: Evaluate requests with a strategic lens to avoid duplicating existing solutions or developing automations that should be managed by other platforms/teams. Actively stay updated with Boston Scientific’s ecosystem of solutions to ensure coherence, scalability, and alignment with regional and global strategies.
• Continuous Improvement: Identify opportunities for efficiency gains, simplification, and digital enablement across multiple functions.
• Collaboration on Integrations: Partner with regional and global IT teams on more complex automation solutions that require integration with core systems (e.g., Salesforce, SAP). Maintain knowledge of APIs, connectors, and integration methods to effectively support these initiatives.
• Documentation & Knowledge Sharing: Produce clear technical and process documentation to support sustainability, compliance, and scalability.
• Collaboration & Change Management: Work with cross-functional teams to support adoption of automation, including end-user training and stakeholder engagement.

• Bachelor’s degree in Engineering, Computer Science, Information Systems, or related field.
• 2+ years of experience with Microsoft Power Platform (Power Apps, Power Automate, Power BI).
• Experience in RPA tools (e.g. Automation Anywhere or others).
• Low-code experience required
• Full-stack experience preferred
• Strong understanding of business process mapping and analysis (Business Analyst exposure a plus).
• Experience with data visualization and reporting.
• Knowledge of APIs, data connectors, and integration principles (to work effectively with regional/global IT teams).
• Demonstrated critical thinking skills in evaluating business needs, assessing solution fit, and identifying risks.
• Ability to manage multiple priorities in a fast-paced, high-performance environment.
• Strong communication skills in English and Spanish; able to translate technical concepts into business language.

• Experience in medical device, pharma, or regulated industries.
• Exposure to Agile methodologies and project management practices.
• Familiarity with compliance, quality systems, and documentation standards.
• Exposure to SAP environments

• A problem solver with curiosity for automation and digital innovation.
• A critical thinker who evaluates requests thoughtfully, balancing speed of delivery with alignment to Boston Scientific’s broader digital ecosystem.
• A team player who embraces Diversity, respecting different perspectives and creating inclusive solutions.
• A structured thinker who demonstrates High Performance by focusing on delivering what matters, with agility and quality.
• A collaborator who practices Care, listening with empathy and acting with integrity to support colleagues and stakeholders.
• A creative innovator inspired by Meaningful Innovation, eager to solve unmet needs and bring ideas into action.
• Someone with a Winning Spirit, who challenges themselves, plays to win, and contributes to Boston Scientific’s mission of advancing science for life.

Costa Rica-Heredia

About the role:

Support the design and development of products, materials, process changes, or new technology for projects with moderate to high complexity. Under minimum supervision/guidance, research data, compiles, analyzes, and reports testing to establish technical specifications for designing or modifying products, processes, and materials.

Your responsibilities include:

• Successfully completes complex engineering work in one or more of the following: product design and development, complex engineering tests and design experiments, preparation of specifications, product capability studies, research investigations, and process/test documentation through the product lifecycle.
• Develop solutions to a variety of problems of high complexity and scope where analysis of situations or data requires a review of identifiable factors.
• Summarizes, analyzes, and draws conclusions from test results. Designs and prepares complex reports to communicate results to the technical community.
• Translates customer needs into product requirements and design specifications.
• Responsible for engineering documentation.
• Works cooperatively with process development, quality, manufacturing, regulatory, clinical, and marketing on complex projects to ensure project success.
• May train, provide work direction, and supervise technicians and entry-level engineers.
• Works under general direction or within a team to complete projects and special assignments.
• Establishes and cultivates a range of business relationships to facilitate the completion of assignments. Influences project team and peers on business solutions.
• Cooperate in determining goals and objectives for projects. May lead projects within the function or department and/or represent the role in larger project teams.
• Performs troubleshooting on product problems related to design, material, or process.

What we are looking for:

• Bachelor's/Licenciature Degree: Mechatronics, Electronics, Electrical, Mechanical, Materials Science, Biomedical, Industrial, Chemical Engineering or related field.
• English level: +90%.
• Experience: +2 years in related positions.
• Knowledge of ISO 13485, MDR, and FDA medical device requirements, including design controls, product life cycle, validation/verification activities, and process improvement.
• Ability to travel internationally.

Work Mode: Onsite

Benefits • Life-Work Integration • Community • Career Growth

Job Title: CRM Field Clinical Representative

Role overview:

In this dynamic and patient-centered role, you will be a key clinical and commercial contributor—supporting our technologies through hands-on education, sales support, and expert clinical guidance. You’ll cover a defined territory, collaborating closely with hospitals and healthcare providers to ensure best-in-class outcomes and to drive the adoption of our innovative CRM solutions.

Your responsibilities will include:

• Serving as the primary clinical expert during device implants, patient follow-ups, programming, and troubleshooting
• Delivering impactful education and training to healthcare professionals on product use and clinical benefits
• Attending procedures in hospital labs and operating rooms to support optimal patient outcomes
• Building strong relationships with physicians, nurses, and key hospital staff to foster trust and drive engagement
• Resolving customer needs efficiently , collaborating cross-functionally to ensure patient and clinician satisfaction
• Managing product inventory according to company guidelines, ensuring readiness and availability
• Participating in a rotational 24/7 on-call schedule to support patients and clinicians in real time

Required qualifications:

• 0–2 years of work experience
• Bachelor’s degree in biomedical engineering, science, math, business, nursing, or equivalent technical field
• Willingness to support a rotating 24/7 on-call schedule, including nights, weekends, and holidays

Preferred qualifications:

• Experience in an electrophysiology (EP) lab, cardiac device clinic, or cardiac catheterization (Cath) lab
• Background in medical device sales, clinical education, or research
• Strong initiative and accountability in achieving goals independently and as part of a team
• Excellent communication skills with the ability to explain complex therapies and technologies clearly
• Passion for innovation, patient care, and collaboration in a fast-paced environment

The anticipated annualized base amount or range for this full time position will be$70,000 to $90,000plus variable compensation governed by the Sales Incentive Compensation Plan (which includes certain annual non-discretionary incentives based on predetermined objectives) as well as the value of core and optional benefits offered at BSC, which can be reviewed at www.bscbenefitsconnect.com. Actual compensation will be commensurate with demonstrable level of experience and training, pertinent education including licensure and certifications, and other relevant business or organizational needs.

For MA positions:It is unlawful to require or administer a lie detector test for employment. Violators are subject to criminal penalties and civil liability.

Please be advised that certain US based positions, including without limitation field sales and service positions that call on hospitals and/or health care centers, require acceptable proof of COVID-19 vaccination status. Candidates will be notified during the interview and selection process if the role(s) for which they have applied require proof of vaccination as a condition of employment. Boston Scientific continues to evaluate its policies and protocols regarding the COVID-19 vaccine and will comply with all applicable state and federal law and healthcare credentialing requirements. As employees of the Company, you will be expected to meet the ongoing requirements for your roles, including any new requirements, should the Company’s policies or protocols change with regard to COVID-19 vaccination.

Among other requirements, Boston Scientific maintains specific prohibited substance testing requirements for safety-sensitive positions. This role is deemed safety-sensitive and, as such, candidates will be subject to a drug test as a pre-employment requirement. The goal of the drug testing is to increase workplace safety in compliance with the applicable law.

About the Role

As the technical and operational leader, you will play a pivotal role in ensuring manufacturing excellence through continuous improvement, systems integration, and advanced troubleshooting. You will be responsible for sustaining process reliability, leading cross-functional teams, and guiding engineering excellence in a high-impact, regulated environment.

Key Responsibilities

· Lead sustaining activities for a complex, mission-critical manufacturing line with a focus on quality, delivery, and compliance.

· Serve as technical authority on integrated systems including PIMS, MES, Power BI, and PLC-based controls (e.g., Allen-Bradley, Siemens).

· Oversee and drive root cause investigations, implement corrective and preventive actions (CAPA), and lead structured problem-solving using DMAIC, 8D, and other lean tools.

· Manage real-time data analytics and reporting using Power BI dashboards, integrating information from MES and other manufacturing systems.

· Own and drive process validations (IQ/OQ/PQ) and ensure regulatory compliance in alignment with BSC Global SOPs and medical device standards.

· Collaborate with cross-functional stakeholders in R&D, Quality, Regulatory, and Supply Chain to resolve technical challenges and optimize line performance.

· Coordinate equipment troubleshooting and optimization, focusing on PLC signal interpretation and system interlocks to ensure seamless automation.

· Lead and mentor a high-performing sustaining engineering team, promoting a culture of technical excellence, ownership, and continuous improvement.

Qualifications

· Bachelor’s degree in mechanical, Electromechanical, Electronic, or Industrial Engineering.

· 5+ years of experience in manufacturing engineering in regulated industries (medical devices strongly preferred).

· Demonstrated success in leading product transfers and sustaining high-impact lines.

· Proficiency in PLC programming and troubleshooting (Allen-Bradley, Siemens).

· Deep understanding of MES/PIMS integration, with capability to leverage Power BI for advanced manufacturing analytics.

· Advanced knowledge of statistical analysis, process improvement, and validation (DOE, Six Sigma, Minitab).

· Strong communication and leadership abilities for cross-site coordination.

· Fluent in English C1+ (90%+).

· Master’s degree in engineering or related field.

· Six Sigma Black Belt Certification.

· Experience navigating SOPs for quality, transfers, and regulatory compliance.

· Take ownership of a strategically critical product with real-world impact.

· Be at the forefront of systems integration, digital manufacturing, and automation.

· Collaborate across global teams and mentor future engineering leaders.

· Work in a state-of-the-art facility with the opportunity to shape the technical roadmap for high-volume, high-quality production.

Costa Rica-Heredia

Hybrid Roles:

About the role:

Develops capable processes and ensures efficient and effective transfer of product into production.

You're Responsabilities include:

• Assesses process capabilities, prioritizes process improvement opportunities, and innovates and implements process improvements on multiple and moderately complex processes.
• Applies technical knowledge to innovate, design, and develop processes, procedures, tooling and/or automation.
• Executes the functional deliverables associated with the PDP/TDP, Project Management, and Quality Systems.
• Ensures proper documentation is completed to meet quality systems requirements. (e.g., BOM’s, Routers, FMEA’s, etc.)
• Develops qualified production lines.
• Additional Duties:
• Oversees development builds associated with the project using special work requests.
• Writes validation protocols and reports applicable to new processes.
• Prepares and presents technical data and recommendations at technical reviews.
• Provides Design for Manufacturability (DFM) input to the engineering print package.
• Contributes ideas to or generates Intellectual Property submissions.
• Trains and/or provides work direction to technicians and may train manufacturing personnel when required as part of a validation.
• May serve as core team member or extended team member on new product projects.

What we're looking for:

• Bachelor or Licenciature degree in Mechanical, Electromechanical, Electronic or related field.
• English Level desired: 70-79%.
• Experience: At least 3 years
• Desired knowledge: Problem Solving, Networking,Statistical skills, Knowledge of Lean manufacturing and Six Sigma, PDP/TDP, Process Validations, Project Management, Knowledge in Quality Systems, Process Improvement.