Research & Development Technician Iii - jobs at Boston Scientific in Costa Rica
Boston Scientific Manufacturing Engineer III Shift C Costa Rica
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Costa Rica-Heredia
About the role:
Evaluates, selects, and applies standard engineering techniques, procedures, and criteria, using judgment in making minor adaptations and modifications. Assignments have clear and specified objectives and require the investigation of a limited number of variables. Improve existing manufacturing processes and act as liaison between production and engineering group in resolving problems encountered on the production floor. Assist with the introduction of new products into the Operations production area.
Your Responsibilities Include:
- Participates in project teams typically including one of the following: identifying and implementing process/product improvement alternatives to increase/optimize yield, efficiency, throughput, and/or performance; designing, performing, and documenting engineering test experiments to evaluate product/product performance; participating in Quality improvement activities; designing, developing, testing, and validating equipment, tools and fixtures; analyzing and interpreting process models and recommending process improvements; evaluates external process technologies; and other activities of limited scope requiring knowledge of principles and techniques commonly employed in the specific narrow area of assignments.
- Participate in equipment and process validation. Write protocols and reports for Equipment Installation Qualification, Operational Qualification and Process Performance Qualification.
- Participate in equipment and process validation. Write protocols and reports for Equipment Installation Qualification, Operational Qualification and Process Performance Qualification.
- Has working knowledge of Risk Management & Failure mode and effect analysis (FMEA) requirements.
- Interfaces with assemblers, production supervisors, and engineers in troubleshooting problems on the production floor.
- Coordinates with the appropriate suppliers and other external resources needed in developing and implementing process/product improvement plans.
- Acts independently to implement and follow through.
- Perform root cause analysis of failed product.
- Participates in project planning and scheduling.
- Optimize processes for yield improvements, cycle time improvements, and scrap reduction.
- Attends and contributes to product core team meetings.
- Performs responsibilities required by the Quality System and other duties as assigned or requested.
What we're looking for:
- Bachelor or Licenciature degree in Mechanical, Electromechanical, Electronic, Electrical Industrial Maintenance or related.
- Experience: At least 3 years
- English Level desired: 70-79%
- Technical Competencies: Problem Solving, Networking, Process Improvement, Lean manufacturing and Six Sigma knowledge, Process Validations.
- Knowledge of the Lab View programming
- Knowledge of automated vision systems
- Work Mode: Onsite.
Benefits • Life-Work Integration • Community • Career Growth
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Boston Scientific Manufacturing Engineer III Shift B Costa Rica
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工作职责：
- 负责区域内客户的手术支持工作并培训相关医院技师，使其能独立配合客户开展手术。
- 与负责区域内的客户建立良好的合作关系，推动区域手术例数及相关产品的应用。
- 为客户提供专业的学术支持，培养并提升客户的手术技能。
- 在直属经理的指导下制定相应的区域管理计划，更好的推动区域手术例数及相关产品的应用。
岗位要求：
- 统招本科及以上学历，2年以上医疗器械工作经验，外企优先；
- 良好的自我驱动力及较强的学习能力
- 良好的沟通技巧、人际交往能力以及团队协作精神
- 诚信，有责任心，富有激情，有创造力，有良好的工作抗压能力
- 能接受高强度跟台，具有电生理相关行业经验者优先
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Boston Scientific Microbiologist III Costa Rica
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Hybrid Roles:
About the Role:
Provide oversight of Microbiology Department for the sustaining operation, support projects requiring microbiology evaluation or testing. Under the direction of the Microbiology Manager, this position will serve as senior matter expert on microbiology, assuring the product meets documented requirements and that processes are controlled and providing support and guidance in the areas of cGMP, Regulatory, technical investigations.
Your Responsibilities Include:
· Strong knowledge of microbiology test methods, standards and regulations governing the quality system and microbiological topics.
· Review and assess from a microbiology context all changes that impact product or the cleanroom environment.
· Support new product development by participating as the microbiology functional team member and represent the Microbiology department on cross-functional project teams as required.
· Support Regulatory submissions by conducting review to ensure appropriate microbiology information is present in the submission.
· Review test reports from internal, external testing for compliance to BSC and external compliance requirements.
· Ensures that products are validated for bioburden and endotoxin testing and support the establishment of routine sampling plans.
· Support Internal/External Audits and ensures all non-conformances are adhered to in a timely manner.
· Provide technical guidance/troubleshooting in the event of Microbiology related issues.
· Act as Quality Engineer for Facilities related matters.
· Revise SOPs and support maintenance of product and environmental documentation.
· Support product bioburden alert limits and cleanroom air and surface alert and action limits periodical revision.
· Organizes and presents data/ information to influence decision making, primarily to internal audiences
What We’re Looking For:
• Degree in Microbiology, Biotecnology or related field.
• At least 3 years of experience in similar position.
• English Level desired: 80-89%.
Benefits • Life-Work Integration • Community • Career Growth
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Boston Scientific Quality Technician III - Shift Cartago Costa Rica
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Our Graduate Programme is designed to accelerate your professional development and provide you with extensive experience within Boston Scientific Clonmel. Throughout the 23 month programme, you will be provided with dedicated mentors and will have professional development 1:1 meetings to provide you with a solid foundation for a successful career. Our Graduate Programme is created around hiring the most innovative and best individuals, while Boston Scientific Clonmel provides the means for you to continuously learn and enhance your skill set to drive your career growth.
Responsibilities
- Works as part of the Global Team to assist in creation and monitoring of project plans, communication and documentation of ways of working (standard processes).
- Works on the Global Implementation of a new Enterprise Resource Planning (ERP) tool SAP S4 HANA.
- Works in the JIRA system to update data on project progress
- Works using Agile & Waterfall project management tools
- Conducts her/ himself as a regular full-time member of the staff by accepting and adhering to Boston Scientific's rules and regulations and by engaging in professional and personable conduct at all times with staff and customers. The intern is also obligated to comply with any confidentiality and professional policies established by the Boston Scientific.
- Becomes knowledgeable about her or his own responsibilities and the business and operational issues inherent in them as well as about the Boston Scientific's management and particular issues relevant to the Company.
- Contributes to the preparation and production of proposals and reports by using word processing, spreadsheets, and other computer programs.
Required
- BSc degree (Honours) in relevant discipline essential.
- Must have graduated within the last two years or in final year of University
- Relevant work experience/ co-op programme completed.
- Eligible to work in IrelandCommunication Skills
- Project Management Skills
** 23 Month Contract ** Closing Date 27th November
Should you require a reasonable accommodation during the recruitment process or after if offered, please let us know.
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Boston Scientific Software Development Engineer Test Costa Rica
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Costa Rica-Heredia
Hybrid Roles:
About the role:
In this pivotal role, you will be expected to leverage your extensive experience to tackle complex technical challenges and drive innovation within the team. Your proactive approach and problem-solving skills will be crucial as you navigate the intricacies of software testing and development. By embracing new technologies and methodologies, you will ensure the robustness and reliability of our software solutions, thereby contributing to our mission of improving patient outcomes through cutting-edge neuromodulation technologies. Your collaboration with cross-functional teams will be instrumental in achieving our strategic goals and delivering high-quality products to the market.
This individual will partner with product development, participate in architectural and software development activities, mentor junior SDET engineers and conduct software requirements analysis, verification, test documentation and automation.
Responsibilities
Being able to extract and create Test Plan by reviewing design documents, technical requirements, andJira stories, and maintaining them during project lifecycle
Creating, maintaining, and refactoring the testing frameworks, implementing test libraries
Creating automated tests inPython using Pytestfor Surface Pro application and mobile integration tests
Familiar with test case management likeJIRAand Zephyrto create test suites, and detailed test steps to ensure requirements traceability and test coverage
Familiar with using general mobile devices to interact with devices via Bluetooth, NFC, Wi-Fi, and using mobile applications to interact with our devices
Comfortable interacting and working directly with Development, Program Management, to get the necessary support regarding key deliverables and interacting with them to resolve issues quickly and efficiently
Being able to reproduce issues reported, or as needed during regression and product verification during testing and after release to production
Willingness to directly work with team members overseas
Proficient oral and written communication skills
Required Qualifications:
4 or more years relevant work experience
2 or more years of Python test development experience
Hands on end-to-end test experience with desktop, windows tablets, mobile and web software products
Experience with testing and supporting large scale customer facing product releases
Practical experience working within an Agile/Scrum based environment
Preferred Qualifications:
Knowledge of wireless testing technologies, including cellular (5G, LTE, WCDMA), Wi-Fi, Bluetooth etc.
Experience with testing complex applications on desktop, tablets
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Boston Scientific Quality Engineer III Costa Rica
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About the role:
Demonstrates commitment to the Quality Policy (patient safety and product quality) through their daily execution of sound quality practices and the maintenance of an effective quality system. Understands and complies with all the regulations governing the quality systems. Ensures their direct reports are aware of their commitment to patient safety and product quality, are current with their training requirements and that they understand and comply with all other regulations governing their work.
You're Responsibilities include:
Lead Products & Processes Transfers from a Quality standpoint.
Identifies and resolves complex exceptions to work assignments.
Summarizes, analyses, draws conclusions and makes appropriate decisions from test results or other process related findings.
Read and interpret technical drawings, procedures, and protocols
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.
Has the responsibility and independent authority to make decisions related to product quality, including the disposition of non-conforming product.
Participates in Customer Complaints investigation for areas under their control.
Continually seeks to drive improvements in product and process quality.
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.
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.
Knowledgeable on QSR and ISO/MDD standards, constantly promoting awareness of best industry practices, making appropriate decision on a daily basis utilizing the quality engineering manager/site QA Director as the final arbitrator on critical quality decisions.
Get involve in various stages of equipment and processes validations: Run and/or review and approve reports: TMVs, I.Q 's, O.Q's and P.Q's as well as any other document relating to validation.
Fully conversant with validation techniques and associated regulatory requirements including analysis of customer feedback and complaints.
Compiles and analyses operational, test and validation data to establish technical specifications and performance standards for newly designed or modified products and processes.
Responsible for reviewing and developing process validation protocols and reports. Support other functional areas during the validation activities.
Evaluates in conjunction with EHS new equipment/processes/chemicals for environmental impact/effect to eliminate or lessen such impacts/effects.
Knowledgeable on Risk Management, ISO EN 14971 requirements.
May participate directly in a new product/technology transfer to ensure compliance to all internal and regulatory requirements.
Uses knowledge of Six Sigma, Statistical Analysis and Lean principles to investigate and solve problems and improve quality.
Gives technical guidance to Associate Quality Engineer, Technician and Inspection staff.
Is a good team member, fully motivated to achieve and demonstrate best practices in line with the department and Site objectives.
Is familiar with the internal auditing process.
What We’re Looking For:
Bachelor's degree in Chemical, Industrial, Electronic, Biotechnology, Electromechanical Engineering or Related Field.
English Level desired: B2 (80-89%)
- Availability to work in our Heredia and Cartago Sites
Experience: proven experience in Medical or Pharmaceutical industry, working on Quality, Process Development or Engineering Department. Solid knowledge in Statistics, Problem Solving techniques, Quality System, Process and Test Method Validation, Risk Management, Six Sigma or similar.
Desired knowledge: Product and Process Transfer and Project Management. ASQ certified desired.
At least 3 years of proven experience in similar position.
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Boston Scientific Equipment Engineer III Costa Rica
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Costa Rica-Heredia
Your Responsibilities Include:
- Responsible for Manufacturing Engineering of a given area.
- Works with Value Stream and Quality Engineering Manager to deliver business objectives – lean manufacturing metrics, VIP, cycle time, scarp as %VOP etc.
- Responsible for developing a world class-manufacturing group that is proficient in problem solving manufacturing issues using Six-Sigma tools.
- Drives IBP (Integrated Business Plan) contract deliverables by providing input on process technology selection.
- Develops and executes departmental budgets and capital spending.
- Leads or represents function in periodic business metric reviews.
- Initiates cross-functional partnerships to identify and resolve production/engineering issues.
- Prioritizes and drives execution of multiple complex department projects. Sponsors and supports Operations Value Improvement Process (VIP) or Strategic Activity Review (STAR) projects.
- Responsible for the departmental basics including budgeting, hiring, day-to-day management, project resourcing, etc.
- Establishes and supports a work environment of continuous improvement that supports BSC’s Quality policy, Quality System & the appropriate regulations for the area.
- Ensures employees are trained to do their work and their training is documented.
- Maintain compliance metrics around adherence to preventative maintenance schedule and calibration schedule.
- Ensure relevant documentation is prepared and updated in line with all Quality and Regulatory guidelines and promotes full compliance to all GMP & ESQ requirements.
- Keep abreast of all relevant technological advancements.
- Maintain and develop the team’s technical and trouble shooting skills.
- Sustain an environment of continuous improvement.
- Develop and maintain relationships with technical management in sister sites and R&D.
- Develop new equipment/processes as necessary.
- Develop and implement the appropriate maintenance procedures and protocols to ensure processes always remain in control.
- Oversee the specification and purchase of capital equipment ensuring balance between optimizing technological capabilities and return on investment.
- Manage the planning and execution of equipment validations per ESQ requirements.
- Providing technical leadership on maintenance and equipment issues.
- Provide effective and responsive Calibration support to Operations to meet their area’s objectives of quality, cost and output.
What We’re Looking For:
- Bachelor’s degree in Mechanical, Electromechanical, Electronic, Electrical Industrial Maintenance or related field.
- English Level: B2 (70% - 79%).
- Desired knowledge: Equipment Maintenance, Process Validations, Execution, Decision-making, Planning, Communication, Quality Oriented, Relationship Building, Innovation
- At least 3 years of experience in similar position.
- 1 year or more in current position.
- Annual Performance evaluation rating "Meets Expectations" or "Exceeds Expectations".
These jobs might be a good fit
Share
Costa Rica-Heredia
About the role:
Evaluates, selects, and applies standard engineering techniques, procedures, and criteria, using judgment in making minor adaptations and modifications. Assignments have clear and specified objectives and require the investigation of a limited number of variables. Improve existing manufacturing processes and act as liaison between production and engineering group in resolving problems encountered on the production floor. Assist with the introduction of new products into the Operations production area.
Your Responsibilities Include:
- Participates in project teams typically including one of the following: identifying and implementing process/product improvement alternatives to increase/optimize yield, efficiency, throughput, and/or performance; designing, performing, and documenting engineering test experiments to evaluate product/product performance; participating in Quality improvement activities; designing, developing, testing, and validating equipment, tools and fixtures; analyzing and interpreting process models and recommending process improvements; evaluates external process technologies; and other activities of limited scope requiring knowledge of principles and techniques commonly employed in the specific narrow area of assignments.
- Participate in equipment and process validation. Write protocols and reports for Equipment Installation Qualification, Operational Qualification and Process Performance Qualification.
- Participate in equipment and process validation. Write protocols and reports for Equipment Installation Qualification, Operational Qualification and Process Performance Qualification.
- Has working knowledge of Risk Management & Failure mode and effect analysis (FMEA) requirements.
- Interfaces with assemblers, production supervisors, and engineers in troubleshooting problems on the production floor.
- Coordinates with the appropriate suppliers and other external resources needed in developing and implementing process/product improvement plans.
- Acts independently to implement and follow through.
- Perform root cause analysis of failed product.
- Participates in project planning and scheduling.
- Optimize processes for yield improvements, cycle time improvements, and scrap reduction.
- Attends and contributes to product core team meetings.
- Performs responsibilities required by the Quality System and other duties as assigned or requested.
What we're looking for:
- Bachelor or Licenciature degree in Mechanical, Electromechanical, Electronic, Electrical Industrial Maintenance or related.
- Experience: At least 3 years
- English Level desired: 70-79%
- Technical Competencies: Problem Solving, Networking, Process Improvement, Lean manufacturing and Six Sigma knowledge, Process Validations.
- Knowledge of the Lab View programming
- Knowledge of automated vision systems
- Work Mode: Onsite.
Benefits • Life-Work Integration • Community • Career Growth
These jobs might be a good fit
