דרושים Training Lead/ Coordinator Emea ב-Boston Scientific ב-הולנד

Your responsibilities will include:

• Interpret and apply relevant cybersecurity standards and regulations (e.g., FDA/CMDE/MDCG Cybersecurity Guidance, IEC 62443, ISO 14971, HIPAA, GDPR) to ensure product compliance.
• Stay current with emerging regulations and standards related to medical device security (e.g., FDA Premarket Guidance, Post-market Cybersecurity Guidance).
• Collaborate with product development teams to embed security controls throughout the design, development, and maintenance phases.

• Self-motivated with a passion for solving problems and a bias for action.

• Ensure that medical device security engineering activities and deliverables (e.g., threat models, security risk assessments, security requirements, security test plans/protocols/reports, SBOM, post-market vulnerability management plans and reports, and cybersecurity labeling) comply with Boston Scientific's global quality system requirements and procedures.
• Collaborate with team on product security needs and requirements; review product security architectures and design specifications.
• Collaborate in planning of software verification and validation strategies.
• Review vulnerability assessments, fuzzing and penetration testing to identify and mitigate risks.
• Ensure continued consistent best practices and processes for secure coding, configuration management, and patching.
• Develop and implement risk mitigation strategies and maintain risk management documentation consistent across the ICTx portfolio.
• Oversee and enhance incident response plans and processes, ensuring rapid and effective resolution of security incidents.
• Drive continuous improvement of vulnerability management, including the evaluation and deployment of necessary patches or updates.
• Work closely with internal stakeholders (Software Development, R&D, Regulatory, IT, etc.) to align on security goals and requirements.
• Participate in internal and external audits, and address findings related to cybersecurity design and risk management processes.

What we’re looking for in you:

Required qualifications

• Bachelor’s degree in Cybersecurity, Computer Science, Computer Engineering, or a related field and 5+ years of experience in cybersecurity engineering, with a focus on product development and risk management or Master’s degree in Cybersecurity, Computer Science, Computer Engineering, or a related field and 3+ years of experience in cybersecurity engineering, with a focus on product development and risk management
• Proven experience leading security design and architecture reviews for complex, embedded medical devices or similar technologies.
• Demonstrated track record of creating and executing security risk assessments and mitigation strategies.
• In-depth understanding of cybersecurity frameworks (e.g., NIST Cybersecurity Framework).
• Understanding of privacy regulations (HIPAA, GDPR) and their intersection with medical device cybersecurity.
• Strong leadership, decision-making, and team-building capabilities.
• Excellent written and verbal communication skills for interfacing with technical teams, stakeholders, and executive leadership.
• Ability to work collaboratively across multidisciplinary teams, bridging gaps between technical, regulatory, and business functions.

Preferred qualifications

• 5+ years of experience working in the medical device industry or a similarly regulated environment; security architecture or medical device administration experience in healthcare settings is also a plus.
• Hands-on experience with secure coding practices, vulnerability scanning tools, fuzzing, and penetration testing methodologies.
• Knowledge of embedded systems security, wireless communications, network protocols, and PKI.
• Familiarity with FDA regulations and guidance documents for medical devices (e.g., 21 CFR Part 820).
• Working knowledge of SW96/TIR57/TIR97, IEC 62304 (software lifecycle), IEC 60601 (electrical safety), and ISO 14971 (risk management).
• Experience supporting VA Handbook 6500 compliance and ISO/IEC 27001 certification.
• Relevant certifications (e.g., GIAC, OffSec, CISSP, CISM, CRISC) are a plus.

Maximum Salary: $ 156900

Compensation fornon-exempt (hourly), non-sales rolesmay also include variable compensation from time to time (e.g., any overtime and shift differential) and annual bonus target (subject to plan eligibility and other requirements).

Compensation forexempt, non-sales rolesmay also include variable compensation, i.e., annual bonus target and long-term incentives (subject to plan eligibility and other requirements).

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

Netherlands-Kerkrade; Belgium-Diegem; France-Île-de-France; Germany-Düsseldorf; Italy-Milan; Spain-Madrid

Field Clinical Engineer– EMEA

About the Role:

The Field Clinical Engineer (FCE) supports a growing department that manages a large pivotal study program based on an innovative medical device technology platform. The FCE will be responsible for all aspects of case support and product education aimed at treating patients with hypertension.

This is a remote position with up to 75% travel required.

Your Responsibilities Will Include:

• Working under general direction, provides engineering, educational, and technical support in response to field inquiries from physicians and health care professionals involving the company’s renal denervation product.
• Performs work that involves a high degree of independence. Identifies and routinely uses the most effective, cost-efficient, and best business practices to execute processes; continually evaluates their effectiveness and appropriateness.
• Exercises independent judgment in planning, organizing, and performing work; monitors performance and reports status to manager.
• Acts as a clinical interface between the medical community and the business.
• Demonstrates ability to build and sustain credible business relationships with customers and shares product expertise accordingly.
• Provides engineering, education, and clinical support in response to field inquiries on an as-needed basis. Demonstrates a thorough command of the TIVUS product , related product and technical knowledge, trends, and players.
• Develops, leads, and/or facilitates trainings and other programs for healthcare professionals.
• Provides insight, guidance, and feedback to management on market feedback and components of next-generation products.
• Provides regional procedural case coverage , potentially across the EMEA region .
• Provides additional back-up support in the following areas:
• Clinical study monitoring/data collection
• Troubleshooting
• New product in-service training to physicians and healthcare professionals
• Continuously develops engineering and technical skills aligned with the company’s strategic goals.
• Assists with advanced educational seminars and preparation of educational materials.
• Assists with advanced product demonstrations to visiting physicians and healthcare professionals.
• Remains current on developments in field(s) of expertise, regulatory requirements, and a good working knowledge of company and competitor products, markets, and objectives as well as industry trends.
• Resolves and/or facilitates resolution of problems, including identifying causes to prevent re-occurrence.
• Performs related functions and responsibilities, on occasion, as assigned.

What Are We Looking For:

• A Bachelor’s degree in Biomedical Engineering, related field, or equivalent healthcare experience.
• A minimum of 5 years of clinical research experience , including coordination of multi-center trials and a solid technical background.
• Fluency in both German and English , written and verbal, to support regional collaboration, training, and communication with internal and external stakeholders.
• Ability and willingness to become certified on the Renal Denervation product .
• Comfortable with extensive travel—up to 75% domestically and within the EMEA region .
• Demonstrated ability to present, write, and teach clinical and medical information effectively.
• Hands-on experience with interventional or catheter-based procedures .
• Strong cross-functional collaboration skills—able to work with engineers, vendors, and customers across various disciplines.
• Proven capability to manage multiple assignments simultaneously while maintaining attention to compliance and detail.
• A proactive approach to identifying and escalating clinical or protocol-related concerns.

Preferred Qualifications:

• Strong communication skills and fluency in medical terminology.
• Clinical research experience specific to the medical device industry.
• Experience in multi-center cardiology trials .
• Familiarity with GCP and ICH guidelines for regulatory compliance.
• Proficiency in Microsoft Office tools and database management systems.

:

Key responsibilities:

• Monitoring compliance with work instructions and work processes.

• Optimal deployment of people as well as supplies based on own knowledge and real-time work offer during the shift.

• Signaling and reporting malfunctions to the Line Facilitator / Maintenance department. Discussing issues with the Supervisor in order to structurally solve malfunctions and other problems during the shift.

• Based on the core metrics; continuous improvement of the workplace and -processes in consultation with the Supervisor.

• Where appropriate, co-conducting PDC conversations in close coordination with Supervisor and providing him/her with input on employee performance.

• Emergency response officer and Emergency response lead during the assigned shift.

:

• Attend to leadership courses

• Experience gained in a warehouse/distribution center or other logistics work environments.

• Good knowledge of and experience with SAP, Word, Excel and Power Point.

• Being able to lead small improvement projects using the BSCI lean essential tools.

• Available for two shifts.

• Good communication skills, spoken and written, in Dutch and English.

:

• Coaching by an experienced team leader

• Expand your talents

• Combine work and education

• Working in an international environment

• Attractive benefits package

• Inspirational colleagues & culture

• Possibility to make an impact

• Fast Growing and innovative environment

So, choosing a career with Boston Scientific (NYSE: BSX) isn’t just business, it’s personal. And if you’re a natural problem-solver with the imagination, determination, and spirit to make a meaningful difference to people worldwide, we encourage you to apply and look forward to connecting with you!

About this role as Supply Chain Planner-EMEA

In this role, you will coordinate and control the EMEA Demand Planning and New Product Launch (NPL) regional forecasting activities to meet customer needs, business requirements, and service level objectives. Additionally, you will support, monitor, and maintain finished goods inventory levels and system integrity.

Your key responsibilities will be:

• SI&OP - Prepare and lead Demand Plan review meetings enabling 24 month rolling forecasts.
• SI&OP - Support Regional Integration & Reconciliation & Exec SI&OP reviews
• Partner and engage with business stakeholders to determine product portfolio and translate decisions into effective inventory strategies to support the agreed service targets
• Perform Inventory Management to meet both Service and Financial objectives, i.e. Safety stock targets setting and Inventory analysis, Potential Stock out, Inventory Projection, Excess & Obsolescence.
• Manage KPI performance incl. Inventory, forecast accuracy and bias, Service Level, Backorder & Scrap. Perform root cause analysis and initiate corrective action.
• Coordinate new product launches and transitions ensuring balancing customer and financial expectations
• Manage product discontinuation ensuring optimal product availability with minimal write off cost
• Identify and manage Value Improvement Projects working with SC functions, Finance and Divisional partners
• Support Annual/Quarterly Finance budget processes: inventory, scrap, ship volume.
• Monthly KPI reporting and ad hoc performance & product availability communication to Business and Corporate functions.
• Manage ERP and APS master data and monitor system integrity.
• Interact with Divisional Marketing, BUM, Finance and Global/ Regional Supply Chain functions

Who are we looking for

• Minimum of 5 years of experience within a supply chain/demand planning environment
• Minimum bachelor’s degree in business or supply chain or equivalent combination of education and experience.
• Good analytics and system skills
• Good communication skills
• Continuous improvement attitude
• Speaks fluently English
• Executes independently

This is a hybrid role which means you will work three days per week at our office in Kerkrade.

Netherlands-Kerkrade; N/A

⦁ Monitoring compliance with work instructions and work processes.
⦁ Optimal deployment of people as well as supplies based on own knowledge and real-time work offer during the shift.
⦁ Signaling and reporting malfunctions to the Line Facilitator / Maintenance department. Discussing issues with the Supervisor in order to structurally solve malfunctions and other problems during the shift.
⦁ Based on the core metrics; continuous improvement of the workplace and -processes in consultation with the Supervisor.
⦁ Where appropriate, co-conducting PDC conversations in close coordination with Supervisor and providing him/her with input on employee performance.
⦁ Emergency response officer and Emergency response lead during the assigned shift.
⦁ During your traineeship start and finish at least an MBO 3 logistics study.
⦁ Attend to leadership courses
⦁ Experience gained in a warehouse/distribution center or other logistics work environments.
⦁ Good knowledge of and experience with SAP, Word, Excel and Power Point.
⦁ Being able to lead small improvement projects using the BSCI lean essential tools.
⦁ Available for two shifts.
⦁ Good communication skills, spoken and written, in Dutch and English.

Netherlands-Kerkrade; Netherlands-Arnhem; Netherlands-Eindhoven; Netherlands-Maastricht; Netherlands-Rotterdam; Netherlands-Utrecht

You fulfil a key commercial role within the hospital accounts in the Southern part of the Netherlands.
The work environment and the focus area are dynamic, developments are evolving rapidly as are treatment options.Your responsibilities include:

• Be accountable for sales and customer satisfaction of the Boston Scientific
  Urology portfolio by managing the hospital accounts in the Southern part of the Dutch market daily.
• Prospect and develop positive relationships with potential and existing healthcare professional customers and other stakeholders (Urologists, OR-Nurse specialists, department managers, biomedical engineers and purchasers) in the assigned accounts.
• Maintain open communication lines with current and prospective customers on programs, promotions and pricing trends.
• Establish, implement and monitor own account plans for the assigned Urology accounts based on BSC business objectives and customer needs. Contributes to the development of annual strategic plan by providing the RSM, NSM and Marketing with detailed business intelligence for accounts in scope (e.g. market size and potential, market / products trends, business opportunities, competitive landscape, updated clinical and economic stakeholders).
• Secure and/or renew existing orders by coordinating communication on product availability, delivery dates, clinical and technical support and inventory levels between customers and Boston scientific customer service.
• Conduct and participate in regional and national marketing & educational training activities to support the development and expansion of relationships and market share.
• Secures ongoing use of Boston Scientific solutions and field clinical support in scheduled Urological procedures in the assigned accounts, by intimate understanding of the workflow and stakeholder requirements, in line with set targets.
• Work with customer service department (devices, disposable and capital equipment specialists) on a daily basis, to ensure superior customer service and product use.
• Keep current on BSC new products or services being offered and give feedback to the corporate stakeholders on market receptivity, concerns or issues learned from the customers.
• Maintain an ongoing knowledge of all aspects of competitive product innovations, sales promotions, catalogs and advertising for personal sales effectiveness and corporate market intelligence.
• Attend industry trade shows and clinical congresses as assigned, responsible for event follow up, including a summary report to sales and marketing management, turning in orders, communicating problems for internal follow up, getting leads and sending appropriate follow-up correspondence.
• Maintain accurate record of sales activities, customer files and field sales reports required, communicating required information as needed. Exerts skills on used systems and processes for account reporting and opportunity planning in the CRM system.
• Creates and maintains accurate overview of replacement dates for existing equipment in order to ensure timely involvement of Boston Scientific in opportunities for renewal of own and replacement of competitor equipment.

What we are looking for:

• Working experience in a sales role with proven track record of success, ideally with experience in Capital equipment sales and (laser) tenders.
• An appetite for commercial excellence and accountability
• Higher Vocational level (HBO) education in a relevant field of healthcare or life sciences.
• Good knowledge of Hospital settings and being fully at ease in an operating room environment.
• Excellent written, verbal and presentation skills in Dutch and English.
• Excellent relationship creation and retainment skills.
• Creative and innovative thinking in meeting customer needs in a profitable manner.
• A pioneering mind and collaborative spirit to help build the Dutch Urology team at Boston Scientific.

What we can offer to you:

• Attractive benefits package - very competitive salary (including 8% holiday pay, 13th month and incentive bonus)
• A company car
• 30 days of annual leave
• A very good pension scheme
• A stock purchase program
• Excellent training/development programmes to influence your career
• Option to lease a (electric) bicycle
• Inspirational colleagues & culture
• Fast Growing and innovative environment
• A team-oriented company culture