דרושים Qa Labs - Microbiology Tech Iii Cartago Shift ב-Boston Scientific ב-קוסטה ריקה

About the role:

This is a highly visible opportunity to serve as the Integration Developer delivering strategic initiatives supporting the HR function. You will own the integration development and implementation responsibilities for our SuccessFactors Integrations product team that designs, develops, tests, deploys, maintains, integrations that flow data to/from our HR platform successfactors. Partnering with HR leadership, and product management team you will be responsible for implementing and supporting various integrations. You’ll work across several globally dispersed teams on some of Boston Scientific’s most critical strategic projects. You will be instrumental in achieving our organization’s goals.

Your responsibilities will include:

• Design and implement integration flows using SAP CPI and BTP.
• Collaborate with functional and technical teams to gather requirements and translate them into integration solutions.
• Develop and maintain APIs and middleware components for HR applications.
• Monitor and troubleshoot integration issues, ensuring high availability and performance.
• Participate in code reviews, testing, and deployment activities.
• Document integration designs, configurations, and support procedures.
• Ensure compliance with data security and privacy standards.
• Ensure that the HR system and related processes meet all applicable compliance requirements
• Ensure adherence to BSC Global Systems methodology and SOX controls
• Ensure Production support tickets are handled within the agreed SLAs
• Work proactively on achieving the VIP goals set for the team.
• Support teams’ growth in Scrum/Kanban methodologies as well as conduct Scrum ceremonies to support enterprise delivery transformation model
• Provide product team reporting/dashboard(s) for senior management in a timely manner

Minimum qualifications:

• Bachelor’s degree in a related field (completed)
• 2+ year of Experience in Design and implement integration flows using SAP CPI and BTP
• 2+ years of Integration Development experience
• Experience in Product Teams and Agile SCRUM methodologies
• Advance English Level

Preferred qualifications:

• Experience in delivering results in large, cross-functional software initiatives
• Experience with SuccessFactors and data integrations processes
• Experience with SuccessFactors implementation and knowledge of different modules in SF
• Experience working on solutions in a controlled environment
• Proficiency in Microsoft Office: Word, Excel, and PowerPoint

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

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

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

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.

Costa Rica-Coyol; Costa Rica-Heredia

Hybrid Roles:

Available Internships

Engineering:Industrial, Mechanical, Chemical or Industrial Chemistry, Electronics, Electromechanical, Mechatronics, Biomedical, Materials, Electrical, Industrial Maintenance and related.

Fluency in English at a level of 60% is required, along with advanced Microsoft Office skills.

This temporary internship, lasting 6-12 months, requires university enrollment throughout the duration.

Desirable qualifications include knowledge in APICS Certification, Basic Microsoft Office, SAP, Inventory Analysis, and Planning.

Internships are available at Heredia and Coyol plants in Costa Rica Hybrid and /or on-site roles. You will have the opportunity to indicate your preference

Duration and Weekly Hours:

30 – 32 hours per week.

Minimum duration of 6 months, extendable to 12 months.

What We Offer

Economic subsidy

On-site meal subsidy

Transportation assistance

2. You'll receive a FORM to fill out for requirements check.

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.