Software Design Assurance Specialist

hace 4 semanas

Barcelona, Barcelona, España Agilent A tiempo completo
About Agilent

Agilent inspires and supports discoveries that advance the quality of life. We provide life science, diagnostic and applied market laboratories worldwide with instruments, services, consumables, applications, and expertise.

Our mission is to help our customers gain confidence in the quality of their DNA, RNA or protein samples in industries such as Biopharma, Clinical Research and Biotech.

Job Summary

We are seeking a Software Design Assurance Specialist to join our Design Quality Group. The successful candidate will provide guidance and expertise on product development and change control to R&D, marketing, procurement and production.

The Software Design Assurance Specialist will ensure data, product and process quality and will provide oversight of design controls, risk management as well as verification and validation activities of our software solutions.

Key Responsibilities
  • Support and engage in new product developments of software
  • Ensure compliance to Agilent's quality management system as part of the product lifecycle
  • Participate in project meetings and design reviews, risk management activities, design transfer, etc.
  • Review of design history files and associated design documents
  • Oversee and support the development of the software test strategy, test scope and test depth
  • Support the development and maintenance of the test automation and regression test suite
  • Support R&D teams on data/information requirements including compliance and security aspects
  • Define appropriate metrics to assess various software attributes such as size, complexity, code coverage and system performance
  • Provide input to verification and validation studies
  • Own, review and approve design control deliverables and changes (ECR/ECO)
  • Act as subject matter expert for software defects or critical issues affecting health/safety
  • Ensure compliance with ISO 9001 and/or ISO 13485, FDA CFR 21 Part 820, ISO 14971, IEC Drive quality compliance projects and continuous improvement activities such as Kaizen, PDCA and Six Sigma
  • Support in audits
  • Provide guidance and/or training to project teams on procedures, design verification and validation, statistical methods, and design controls
Requirements
  • Bachelor's or Master's degree preferred in software engineering, business informatics or equivalent
  • 4 years of relevant experience in the areas of product development and/or quality engineering using waterfall and agile methodologies (Scrum, Kanban)
  • Work experience under ISO 9001, ISO 13485, and/or ISO 62304 as well as relevant cybersecurity standards and data integrity compliance
  • Hands-on-experience with test automation infrastructure preferred
  • Hands on experience with coding languages like Type Script, C#, JavaScript, Python, VB Script preferred
  • Experience with system architecture designs including embedded systems, client-server, n-tier, web and teamwork platforms preferred
  • Understanding of software project lifecycles, test processes and tools such as JIRA- ISTQB Certification preferred
  • Experience with laboratory equipment in the genomics field preferred with the ability to communicate and understand biological and clinical applications (Bioanalyzer, TapeStation, Fragment Analyzer, Gel or Capillary Electrophoresis or Liquid Chromatography)
  • Experience in quality requirements for medical devices and data integrity compliance and workflows preferred ( 21 CFR part 11, ISO experience with multi-national and interdisciplinary teams in a matrix organization
  • Pragmatic, flexible and solution-oriented
  • Good planning and communication skills
  • Able to make independent decisions within guidelines of the organization.
  • Familiar with good documentation standards
  • Strong skilled in exchanging communication and providing technical guidance in English
  • Good understanding of statistical methods preferred
About the Role

This job has a full time weekly schedule.

Our pay ranges are determined by role, level, and location.

Within the range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training.

During the hiring process, a recruiter can share more about the specific pay range for a preferred location.

Pay and benefit information by country are available at: Agilent Technologies Inc. is an equal opportunity employer.

Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other protected categories under all applicable laws.

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