Sr. Staff Quality Engineer - New Product Development
Onsite, Durham, NC
- 求人ID
- R-528862
- Category
- Engineering
- Location
- ダーラム, ノースカロライナ州
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。
Job Description Summary
We have an immediate opening for a highly motivated, results-focused professional to join our team, and are growing our staff as a Senior Staff Quality Engineer. The Quality Engineer's primary responsibilities are to support new product development activities, maintain compliance to company procedures and external standards, manage design history files, review design artifacts, participate in risk analysis activities, collaborate on product development deliverable documentation, support failure investigations, identify system issues, summarize findings and prepare reports for key quality metrics.Please note this role is in the Quality organization and has no direct responsibility for software testing (V&V).
Job Description
We are the makers of possible
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.
We believe that the human element, across our global teams, is what allows us to continually evolve. Join us and discover an environment in which you’ll be supported to learn, grow and become your best self. Become a maker of possible with us.
The Senior Staff Quality Engineer is a key member of the New Product Development Team and is responsible for QA-related R&D activities from research through product launch. This position ensures that design controls and risk management principles are applied to new product development and sustaining engineering projects. This position also supports broader QMS activities (Audit, CAPA, Data Analysis, Installation & Servicing, Complaint Handling, etc.).
Business & Product Overview
BD’s Pharmacy Automation Central Fill solutions are designed to transform high-volume prescription fulfillment into a streamlined, error-reducing, and scalable operation. These centralized facilities serve networks of retail pharmacies, hospital systems, care facilities, and mail-order services, enabling efficient medication distribution from a single location.
Responsibilities
- Serve as the quality cornerstone for multi-functional design teams, championing excellence in both new product development and sustaining engineering efforts
- Orchestrate comprehensive quality strategies throughout the design control lifecycle—from initial planning through verification and validation to risk management and regulatory compliance
- Provide expert guidance on quality system implementation, with specialized focus on design controls
- Conduct thorough reviews of design documentation, ensuring meticulous compliance with Quality Management System requirements and documentation protocols prior to final approval
- Partner strategically with program management to synchronize design achievements and enable successful commercial launches across markets
- Ensure robust verification and validation protocols that definitively confirm design specifications and requirements
- Maintain comprehensive traceability matrices across all design elements, creating a clear line of sight from requirements to implementation
- Give vital quality insights during product requirement development, system hazard analysis, and critical design reviews
- Build collaborative partnerships across functions to drive consensus and resolve sophisticated challenges efficiently
- Lead sophisticated root cause investigations and structured problem-solving initiatives for both development and manufacturing challenges
- Curate impeccable technical files and Design History Files that withstand regulatory scrutiny
- Orchestrate continuous improvement initiatives by facilitating multi-functional collaboration and innovation
- Demonstrate mastery of quality engineering principles, methodologies, and industry standards
- Apply comprehensive understanding of regulatory frameworks and international standards—including EU MDR 2017/745, ISO 9001, ISO 14971, and IEC 62304—with minimal direction
- Leverage deep knowledge of software quality assurance throughout the development lifecycle
- Proactively identify potential risks and collaborate with program teams to document and implement effective mitigation strategies
- Use advasophisticatedlity engineering tools including statistical analysis, sampling methodologies, and root cause investigation techniques
- Serve as a mentor and knowledge resource for developing quality professionals
Differentiating Qualities
These specialized experiences will set you apart as a candidate:
- Demonstrated success applying Lean or Six Sigma methodologies to streamline software design control processes, with practical implementation examples
- Experience championing cybersecurity initiatives within regulated medical device environments
- Consistent track record supporting hardware development and integrating hardware/software systems within design controls frameworks
- Great foundation in modern software development methodologies
- Experience thriving in iterative development environments such as Scaled Agile Framework (SAFe), particularly with SAFe certifications
- Comprehensive understanding of risk management principles and quality-by-design approaches
Qualifications:
- Bachelor’s degree in a relevant degree field such as engineering and 15 years’ experience with emphasis on R&D development, Quality Engineering and Design Controls OR
- Master’s degree in a relevant degree field such as engineering and 10 years’ experience with emphasis on R&D development, Quality Engineering and Design Controls
- Ability to travel up to 10%
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.
Why Join Us?
A career at BD means being part of a team that values your opinions and contributions and that encourages you to bring your authentic self to work. It’s also a place where we help each other be great, we do what’s right, we hold each other accountable, and learn and improve every day.
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 health. At BD, you’ll discover a culture in which you can learn, grow, and thrive. And find satisfaction in doing your part to make the world a better place.
To learn more about BD visit https://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.
#BDCLO
Required Skills
Optional Skills
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Primary Work Location
USA NC - Durham - Roche DriveAdditional Locations
Work Shift
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
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「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。」
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「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。」
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「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。」
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「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。」
福利厚生
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競争力のある報酬
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退職金制度
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医療保険
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有給休暇
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育児休暇
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従業員支援プログラム(EAP)
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報奨・表彰制度
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