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Automation & Equipment Engineer

Onsite, Canaan, CT

応募
Job ID
R-549456
Category
Engineering
Location
Canaan, コネチカット州

イノベーション、オーナーシップ、そしてヘルスケアの前進に貢献するエンジニアリングのキャリアを築く

BDのエンジニアリング・R&Dは、世界中の医療提供のあり方を形づくるテクノロジーを設計し、開発し、改良しています。あなたは科学的思考、技術的専門性、創造的な問題解決力を活かして、複雑な課題を意義あるソリューションに変えていくことになります。

機械、電気、プロセス、システム、ソフトウェア、リサーチエンジニアリングなど、どの分野を専門とされていても、BDにはイノベーションを推進するための規模、リソース、そして自由があります。明確な期待値、成果に対する責任、そして業界をリードするテクノロジーとともにキャリアを成長させる機会があります。

そして、世界最大級のメドテックカンパニーの一員として、グローバルなヘルスケアシステムに広く届けられるソリューションを形づくり、大規模に人々の生活を向上させていくことになります。

We are the people who give possibilities purpose

BD is one of the largest global medical technology companies in the world. Advancing the world of health™ is our Purpose, and it’s no small feat. It takes the imagination and passion of all of us—from design and engineering to the manufacturing and marketing of our billions of MedTech products per year—to look at the impossible and find transformative solutions that turn dreams into possibilities.

Job Description

Responsibilities

Partner with cross-functional teams to ensure equipment, processes, and products are designed, delivered, and operated to the highest standards of quality, efficiency, safety, and compliance:

  • Product Design: Ensure products are designed for efficient manufacturing, target cost of goods (COGS), and required quality standards.
  • Unit Quality: Ensure equipment design and manufacturing comply with regulatory requirements and industry standards.
  • Production: Design equipment that supports efficient manufacturing, is easy to operate and maintain, and consistently achieves production targets.
  • Maintenance & Engineering: Maximize equipment uptime through reliable, maintainable designs and adherence to preventive maintenance practices.
  • Procurement & Suppliers: Ensure components meet quality and safety standards while remaining cost-effective and readily available.
  • Plant Quality: Monitor equipment performance to ensure products consistently meet quality and regulatory requirements.
  • Program Management: Deliver projects on time, within budget, and aligned with business requirements.
  • Finance: Support capital planning, forecasting, budgeting, and reporting activities.

Process & Equipment Design and Development

  • Lead the design and development of assembly, packaging, automation, inspection, and manufacturing equipment, including mechanical, electrical, controls, robotics, vision, and software systems.
  • Convert product, process, quality, and capacity requirements into scalable equipment and automation solutions.
  • Create, review, and maintain User Requirement Specifications (URS) aligned with manufacturing, quality, regulatory, safety, and business needs.
  • Evaluate multiple design concepts by balancing risk, reliability, scalability, standardization, cost, and lifecycle impact.
  • Develop innovative automation and mechanical system concepts while incorporating industry trends and company standards.
  • Create, review, and approve equipment layouts, system architectures, 3D models, and engineering drawings.
  • Perform engineering analyses and simulations to validate and optimize designs.
  • Lead design reviews, risk assessments, machine safety evaluations, and FMEA activities.
  • Establish and verify relationships between Key Process Input Variables (KPIVs) and Key Process Output Variables (KPOVs).
  • Support Proof of Concept (POC) and Design of Experiments (DOE) activities to define process capability and operating windows.
  • Optimize equipment for manufacturability, ergonomics, maintainability, reliability, and overall cost of ownership.
  • Leverage production data to drive new equipment designs and continuous improvement initiatives.
  • Provide technical and financial input for capital investment justifications and business cases.

Supplier & Capital Project Leadership

  • Lead equipment suppliers, system integrators, and external vendors throughout the project lifecycle.
  • Partner with Procurement on supplier selection, RFQs, technical evaluations, and risk assessments.
  • Define and manage supplier scope, costs, timelines, deliverables, and technical requirements.
  • Review and approve supplier-generated designs, schematics, software architecture, and safety systems.
  • Plan, witness, and approve Factory Acceptance Testing (FAT).
  • Drive corrective actions, engineering changes, and supplier performance improvements.
  • Support contract execution, change management, and claims resolution.
  • Build and maintain strong relationships with key equipment manufacturers and technology partners.

Equipment Integration, Validation & Start-Up

  • Lead the integration of new equipment and processes into existing manufacturing operations.
  • Develop installation and integration plans, including site readiness, utilities, logistics, safety, and resource requirements.
  • Support Site Acceptance Testing (SAT), commissioning, and handover activities.
  • Execute equipment qualification, process verification, and validation activities in compliance with quality and regulatory requirements.
  • Ensure validation protocols, reports, and documentation are completed and approved.
  • Manage start-up execution to ensure readiness of equipment, documentation, processes, materials, and personnel.
  • Develop training programs, standard work, and operational procedures before production handoff.
  • Minimize operational disruptions during equipment installation, upgrades, and software implementations.
  • Troubleshoot and resolve equipment, automation, and process issues using structured problem-solving methodologies.

Ramp-Up, Performance Management & Continuous Improvement

  • Provide technical leadership during production ramp-up to achieve performance, quality, and capacity targets.
  • Lead centerlining activities to stabilize and optimize manufacturing processes.
  • Measure and analyze performance gaps against expected outcomes.
  • Develop and implement corrective actions to improve long-term equipment performance and reliability.
  • Identify and implement opportunities to enhance equipment design, validation strategies, and integration methods.
  • Support Lean Manufacturing, process optimization, and continuous improvement initiatives.

Documentation, Training & Handover

  • Ensure complete and accurate documentation for equipment, validation, maintenance, controls, and operating systems.
  • Support the creation of operating procedures, troubleshooting guides, maintenance plans, and standard work instructions.
  • Deliver training programs for operators, engineers, maintenance personnel, and quality teams.
  • Execute formal handover to Operations, Maintenance, Engineering, and Quality teams for long-term production support.

Compliance, Safety & Quality

  • Ensure all equipment, installations, and modifications comply with EHS requirements, machine safety standards, and company policies.
  • Maintain compliance with GMP, ISO, FDA, and Quality System requirements throughout design, validation, and production.
  • Support internal and external audits, regulatory inspections, and compliance reviews.
  • Champion a strong culture of safety, quality, and regulatory excellence across all project phases.

Leadership, Mentoring & Collaboration

  • Provide technical guidance, coaching, and mentorship to engineers and project team members.
  • Lead technical decision-making and collaboration across global, cross-functional teams.
  • Support global standardization initiatives, best practice sharing, and knowledge transfer across manufacturing sites.

Required Qualifications:

  • Bachelor’s Degree in Mechanical Engineering, Controls Engineering or related field, or relevant equivalent experience.

  • 3+ years in automation / procurement and assembly and packaging experience

  • Experience leading projects end to end.

  • Willingness and ability to travel domestically and internationally up to 25%.

Preferred Qualifications:

  • Experience in SolidWorks or other 3d modeling software

  • Previous experience with Good Manufacturing Practice (GMP), ISO standards and Lean Manufacturing concepts.

  • Experience in an FDA regulated quality environment

Knowledge and Skills:

  • Excellent technical skills including project management, organization, planning, and capital budgets.

  • Demonstrated ability to apply problem solving and data analysis methods.

  • Strong communication skills

  • Risk analysis / FMEA

At BD, we prioritize on-site collaboration because we believe it fosters creativity, innovation, and effective problem-solving, which are essential in the fast-paced healthcare industry. For most roles, we require a minimum of 4 days of in-office presence per week to maintain our culture of excellence and ensure smooth operations, while also recognizing the importance of flexibility and work-life balance. Remote or field-based positions will have different workplace arrangements which will be indicated in the job posting.

For certain roles at BD, employment is contingent upon the Company’s receipt of sufficient proof that you are fully vaccinated against COVID-19. In some locations, testing for COVID-19 may be available and/or required. Consistent with BD’s Workplace Accommodations Policy, requests for accommodation will be considered pursuant to applicable law.

#CLOLI

Why Join Us?

To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of healthcare. At BD, you’ll discover a culture in which you can learn, grow and thrive.

We believe that when people connect in person, we learn faster, collaborate more deeply, and build a stronger culture. Join us and enjoy a culture where face-to-face collaboration supports your learning, your progress, and your success.

To learn more about BD visithttps://bd.com/careers.

Becton, Dickinson, and Company is an Equal Opportunity Employer. We evaluate applicants without regard to race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, and other legally protected characteristics.

Required Skills

Optional Skills

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Primary Work Location

USA CT - Canaan

Additional Locations

Work Shift

応募

求められる人物像

BDのエンジニアリング・R&D部門で活躍する人たちには、どのような特長があるでしょうか。以下のような方は、BDのエンジニアリング・R&D部門できっと活躍できるはずです:

  • 分析力のある方
  • 協働的な方
  • 探究心・好奇心旺盛な方
  • 細部にまで注意を払える方
  • 創造力のある方
  • 問題解決力のある方

次のチャレンジの準備はできていますか?

ここは、大胆な発想と精密な実行を両立させたいエンジニアのための環境です。あなたは設計の意思決定に影響を与え、製品ライフサイクル全体に関わり、あなたの仕事がコンセプトから実際の世界でのインパクトへとつながる過程を見届けることができます。そのすべては、グローバルメドテックリーダーとしての規模によって支えられています

BDイノベーターの一人から、BDがどのように最先端のAIや機械学習を活用して、患者アウトカムを改善し、医療アクセスを拡大する意思決定を推進しているかをお聞きください。ここでは、あなたの仕事が世界中でリアルタイムにインパクトを生み出します。

人を中心に築かれた職場環境

  • 「BDは大きなグローバルカンパニーなので、周囲の人とつながり、積極的に連絡を取ることをためらわないで欲しいです。ここには学べることが本当にたくさんありますし、会社は人の育成と成長に手厚く支援をしてくれます。スポンジのようになって、できるだけ多くの知識を吸収し、自分のキャリアブループリントを最大限に活かしてほしいと思います。私は自分の仕事が本当に大好きで、BDで働けることにとても感謝しています。」

  • 「アイルランドのリサーチセンターでは、30カ国以上の国籍の人たちが働いていると思います。これはとても素晴らしいことで、BDについて私が最も気に入っていることの一つです。私は電気エンジニア、機械エンジニア、科学者など、多くの人々と仕事をしています。一日を通して非常に多様な視点を見聞きできることは素晴らしいことです。」

  • 「メドテック分野で私たちがどのようにイノベーションを続けているのか、今でも驚かされています。医療従事者にさらに多くのソリューションを届けるにはどうすべきか、技術の効率性をどのように高めるか、常に検討しています。そのすべてを、患者さんへの影響を念頭に置きながら行っています。BDで意義のある仕事を見つけられただけでなく、自分が活躍できる場所を見つけました。」

  • 「面接のときに、私たちの輸液ソリューションが世界中でどれほど大きな影響を与えているかを知り、感銘を受けました。鎮痛剤、がん治療、麻酔、その他の治療など、いずれであっても、自分の家族の誰かがBDの製品を使っている可能性は高いのです。ヘルスケアにこれほど大きなインパクトを与えることのできる製品の開発に携われることは、誇らしいことです。私はBDでの自分の役割が大好きです。」

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