Zimmer Biomet Holdings

Systems Designer

Zimmer Biomet Holdings$80K — $100K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • 5-7 years of experience in software development or design, preferably in an Agile setting.
  • Experience in software verification/validation, ideally in a regulated environment.
  • Familiarity with Agile practices such as Scrum and SAFe; certification as a Scrum Master is a plus.
  • Knowledge of 21 CFR Part 11 and 21 CFR 820 regulations.
  • Bachelor's degree in engineering (computer, software, biomedical, or equivalent).
  • Bilingual in French and English; strong written and verbal communication skills.
  • Proven analytical skills and ability to manage priorities effectively.

Responsibilities

  • Analyze client needs and define software system specifications considering functional and technical requirements.
  • Write quality documentation for product design and development, ensuring compliance with standards and procedures.
  • Plan, coordinate, and support software verification and validation, including test documentation and execution.
  • Collaborate with various teams to validate new technologies and foster innovation.
  • Assist in the implementation of systems and provide training and user support.
  • Maintain existing products through preventive and corrective actions.

Benefits

  • Stimulating work environment fostering creativity and collaboration.
  • Highly competitive advantages and benefits package.
  • Opportunity to contribute to innovative medical solutions that improve lives.
  • End-to-end development responsibility in a supportive Agile team.
Full Job Description
Nous sommes à la recherche d'une personne passionnée, capable de travailler en collaboration avec divers acteurs et équipes et ce, de façon autonome. En tant que concepteur/analyste de système, vous aurez l'occasion de participer, au sein de l'équipe de développement de produits, à toutes les étapes du processus de recherche et développement, y compris l'analyse, la conception et la mise en marché.

Plus précisément, à ce poste :
• Vous analyserez les besoins auprès des clients et définirez les spécifications du système logiciel en tenant compte des exigences fonctionnelles et techniques.
• Vous rédigerez les documents qualité liés à la conception et au développement de produits et veillerez au respect des normes/procédures applicables, garantissant la qualité et la sécurité des produits.
• Vous participerez à planifier, coordonner et supporter l'exécution de la vérification et validation du produit logiciel, incluant la documentation et l'exécution des tests pour chacune des composantes.
• Vous interagirez avec les différentes équipes pour valider de nouvelles technologies et maintenir l'innovation.
• Vous participerez à l'implantation des systèmes ainsi qu'à la formation et au support des utilisateurs pour notre système.
• Vous participerez à la maintenance des produits existants en menant des actions préventives et correctives.

Ce qui fera la différence
• On vous reconnaît pour votre aisance à interagir avec des collaborateurs tant à l'interne qu'à l'externe, ainsi qu'à comprendre et vulgariser des sujets techniques complexes.
• Vous êtes une personne dotée d'un excellent esprit d'analyse et d'une excellente capacité de gestion des priorités et des échéanciers.
• Vous êtes bilingue (français et anglais), tant à l'oral qu'à l'écrit.
• Intérêt pour le domaine médical
• Créativité et penchant pour la résolution de problèmes
• Autonomie, habiletés interpersonnelles et capacité à travailler en équipe
• Excellentes aptitudes de communication orale et écrite

Votre parcours
• Expérience en développement logiciel ou conception logicielle dans un milieu Agile
• Expérience en tant que spécialiste vérification/validation logicielle dans un milieu Agile
• Expérience en pratiques agiles Scrum et Scaled (SAFe) (certification et expérience en tant que Scrum Master, un atout)
• Connaissances des réglementations 21 CFR Part 11, 21 CFR 820
• Vous possédez un diplôme d'études universitaires en génie (informatique, logiciel, biomédical ou équivalent).
• Vous possédez au moins 3 années d'expérience en développement de produits (business analyst) ou en validation, idéalement de systèmes logiciels ou dans un domaine hautement réglementé (médical, aéronautique ou pharmaceutique).

What You Can Expect

Do you want to push the boundaries of innovation and help improve people's lives? Zimmer Biomet develops innovative solutions for orthopedic treatments and surgeries, enabling thousands of people around the world to regain mobility and an active life. Zimmer Biomet is a world leader in medical devices specializing in musculoskeletal care. In Montreal, Zimmer CAS represents the high-tech arm of Zimmer Biomet.

Our software development team stands out for its creative and friendly atmosphere, its rigorous development process and its capacity for innovation, following the Agile development methodology. Our mandate supports the medical products offered by Zimmer Biomet; projects include but are not limited to logistics systems integration, patient data management, surgery planning, business intelligence and web systems. Within our Agile team, we develop web services and web applications for the worldwide orthopaedic surgery planning, including the design and e-manufacturing flow of the Patient Implant. Our system is the backbone on which rely many other medical devices including the now famous Zimmer Biomet ROSA Surgical Robot. Our team is responsible for the end-to-end development and maintenance of our system with its on-premises and Cloud infrastructures.

Renowned for offering a stimulating work environment and highly competitive advantages and benefits, our company is looking for a dynamic, versatile person who is inspired by collaboration in a multidisciplinary team.

How You'll Create Impact

We are looking for an enthusiastic individual, with great interpersonal skills to facilitate the numerous collaborations with teams and clients. As Systems Designer/business analyst, you will actively participate as part of the product development team in all stages of the software development process, including analysis, design, implementation, and release.

Specifically, in this role you will:
• Analyze business needs and define software system specifications, while considering technical and functional requirements.
• Write high quality design and product development documentation and ensure compliance with all applicable standards and procedures, in order to guarantee the quality and security of the system.
• Participate in planning, coordinating, and supporting the execution of the verification and validation of the software product, including the documentation of the tests for each of the components and their execution.
• Interact with different teams to validate new technologies implementation and maintain innovation.
• Participate in implementation of systems as well as training and customer support for our system.
• Participate in maintenance of existing products by carrying out preventive and corrective actions.

About Zimmer Biomet Holdings

Zimmer Biomet Holdings is a global leader in musculoskeletal healthcare. The company designs, manufactures, and markets orthopedic reconstructive products, sports medicine, biologics, extremities, and trauma products. Zimmer Biomet serves healthcare professionals and patients in more than 100 countries. The company is committed to improving patient outcomes and has a strong focus on innovation and sustainability.
Learn more about Zimmer Biomet Holdings
Size
19,500 employees
Market Cap
$26.7 billion
Industry
Net Income
-$138.9 million
Founded
1927
5 Year Trend
+0.4%
Revenue
$7 billion
NASDAQ

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