どんな仕事かAIによる生成

Senior Systems Engineerとして、輸液技術の新製品開発および既存製品の維持・改善を担当します。エンジニアリング、品質、規制、ソフトウェア、製造などの多職種チームと連携し、システム要件、設計、統合、検証・妥当性確認を進めます。勤務地はリムリックで、米国チームとも協働します。

応募資格

Bachelor of Engineering or Science Degree with a strong technical background within Systems Engineering, medical device development, or similar roles.
Ability to work in a team with global collaboration and interacting with external development partners.
Excellent communication and written skills with attention to detail.
Experience in multiple areas within Systems Engineering such as; requirements development and management, system architectural planning and design, interface control, systems integration and characterization testing.

Experience interpreting experimental results, performing statistical analysis or DFSS (Design for Six Sigma) techniques and FMEA methods is a plus.
Experience with requirements management tools such as Microsoft Azure/Modern Requirements is a plus.
Experience in development to IEC 60601 and IEC 62304 standards is a plus.

職種: ITアーキテクト・システムアーキテクト
雇用形態: 記載なし
役職: Senior Systems Engineer
給与: 記載なし
給与の詳細: €56,600.00 - €86,300.00 EUR Annual
勤務地: IRL Limerick - Castletroy
働き方: In-Office, Limerick, MunsterPlease note:** this role is based at our Limerick site, where you will be required to be on site 4 days per week.
学歴: 大学卒業以上
掲載日: 2026/10/05 21:09（1日前）
最終確認: 2026/10/05 21:09（1日前）

BD are looking for a Senior Systems Engineer to join our Limerick team, working alongside our USA team; supporting the development and sustainment of advanced infusion technologies. This is a great opportunity to work on complex electromechanical products within a global, multi-functional environment, influencing products that make a significant difference to patients and healthcare professionals worldwide.
As a Senior Systems Engineer, you will play an important role in driving both new product development (NPD) and product sustainment activities across our infusion portfolio.
Working with multidisciplinary teams spanning engineering, quality, regulatory, product management, software, electronics, manufacturing, and external partners, you will ensure robust system-level design, integration, verification, and validation throughout the product lifecycle.
You will be a technical leader, capable of translating diverse stakeholder inputs into clear system requirements while balancing technical trade-offs, quality expectations, and regulatory obligations.
As part of a global engineering organisation, you'll collaborate regularly with teams in the United States. Flexibility to adjust working hours when needed for cross-regional meetings and project activities will be important to ensure successful partnership and delivery.

Plan through all project phases, strategy and execution of product development, design verification and validation.
Has a strong background in electromechanical medical device, IVD or lab automation design and development.
Can translate multiple design inputs from User Needs, Regulatory, Quality, Marketing, Product Security etc., into product requirements, specifications and detailed trace matrices.
Can critically assess the design and test implications for product requirements and specifications.
Responsible for coordination of system-level product development; requirements, architecture, integration and system characterization testing.
Can challenge design proposals and prototypes through robust design reviews.
Concisely communicates technical challenges and possible solutions and manages key decisions and tradeoffs.
Guides in identifying key system behavior issues and driving the implementation of their solutions for new and existing products.
Establishes courses of action and plans for self and others to ensure that work is completed efficiently.
Develops and sustains productive business relationships on a global front.
Shares Systems Engineering knowledge expertise with junior level team members and other functional areas as domain specialist.

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