J

Jabil

Designs and builds electronics for other brands

Quality Systems Engineer-CSV Specialist

Validation, Compliance & Quality SystemsConfirmed live in the last 24 hours
Full-timeDevens, MA, USA

About the Job

Requirements

  • A bachelor's degree in Engineering, Science, or a related discipline is preferred.
  • One to two years of software validation experience is required; experience in the medical device or pharmaceutical industry is preferred, though knowledge from any industry is acceptable.
  • Knowledge of ISO 13485 and FDA Part 820 is preferred.
  • Demonstrated working knowledge of computer software validation practices and requirements in a regulated medical device manufacturing environment is preferred, including 21 CFR Part 820, 21 CFR Part 11, ISO 13485, Good Documentation Practices, and Good Manufacturing Practices.
  • Applicants must be legally authorized to work in the United States without current or future sponsorship by Jabil.
  • The role requires attention to detail, follow-through, organizational skills, self-motivation, and the ability to work independently with minimal supervision or guidance.

Responsibilities

  • Function as the site subject matter expert for computer software validation, data integrity, and GxP computerized systems for Clinton/Devens, providing governance and oversight of the validation lifecycle of regulated software systems.
  • Lead and support software validation projects, perform risk assessments for new systems and periodic reviews for existing systems, and maintain a site inventory of GxP-impacting systems.
  • Collaborate cross-functionally with departments to develop and improve software systems and maintain harmonization with the Jabil Global Team.
  • Own, develop, and maintain quality management system documentation for the computer software validation process.
  • Maintain the GxP system inventory identifying software used by the Clinton/Devens site.
  • Lead the periodic review process, including user access reviews for software systems used at the site.
  • Coordinate with information technology when hardware or software upgrades are needed.
  • Support and guide users on software validation activities.
  • Serve as the site computer software validation and data integrity subject matter expert, providing guidance and support during audits, investigations, corrective and preventive actions, and compliance activities.
  • Act as secondary owner for quality management system and learning management system software, supporting site administration, maintenance, and adherence to applicable regulatory and customer requirements.
  • Author, review, and approve documents such as user requirement specifications, validation plans, risk assessments, test protocols and reports, and validation summary reports.
  • Ensure compliant use of change notices for documentation submissions and changes.
  • Participate in problem-solving and process improvement activities.
  • Support programs and initiatives related to the Jabil Healthcare Ethics Code, values, and sustainability programs.
  • Perform other responsibilities as assigned based on company evolution and department or position requirements.

Desired Qualifications

  • Preferred experience in the medical device or pharmaceutical industry.
  • Knowledge of ISO 13485 and FDA Part 820 is preferred.
  • Working knowledge of computer software validation practices and requirements in regulated medical device manufacturing is preferred, including 21 CFR Part 820, 21 CFR Part 11, ISO 13485, Good Documentation Practices, and Good Manufacturing Practices.

About the Company

Jabil

Designs and builds electronics for other brands

Jabil designs and manufactures electronics and other products for companies that sell them under their own brands, including makers of AI data center hardware, medical devices, cars, and defense systems. Customers bring a product idea or design, and Jabil handles the engineering, sources the parts, builds the product at scale, and manages the supply chain behind it. The work runs through a global network of factories, so one partner can build products for customers across many markets, from data center racks to medical equipment. Jabil earns revenue through manufacturing and engineering service contracts with these brands. The company was founded in 1966 and is based in St. Petersburg, Florida.

Company size
10,001+
Company stage
IPO
Headquarters
Saint Petersburg, Florida
Founded
1966

Recently Posted Jobs

Explore more opportunities at Jabil

See more jobs