Senior Quality Engineer

Johnson & Johnson Johnson & Johnson · Pharma · Jacksonville, FL +1

Senior Quality Engineer role focused on software validation (CSV) for manufacturing processes in the medical device industry. Responsibilities include planning, documentation review, cross-functional collaboration, change control, and audit support within a regulated environment adhering to FDA and European regulations.

What you'd actually do

  1. Support Computer Software Validation (CSV) project planning activities including the creation or updates to URS, SDS and RTM documents.
  2. Review and approve software validation documentation, such as qualification protocols, reports, software test scripts, risk analysis, and code reviews.
  3. Work multi-functionally with Engineering, Operations, R&D and other groups to plan and complete validations on current and new processes for operational integration.
  4. Facilitate software changes as part of the Change Control Board (CCB) as the SQE representative.
  5. Support the Installation Qualification (IQ) of manufacturing lines.

Skills

Required

  • Bachelor’s Degree in Engineering, Computer Science or STEM related field
  • six (6) years of experience in a regulated environment
  • Working knowledge of software validation requirements for software used in the production of medical devices and software used to support the Quality System
  • Working knowledge of FDA and European medical device regulations (QSR and ISO)
  • Working knowledge of GAMP5 and SDLC
  • Working knowledge of Part 11 regulations for electronic records, electronic signatures, and data integrity
  • Experience with SCADA, PLC, HMI, Vision Systems, and/or Manufacturing Execution Systems (MES) and experience working in manufacturing/operations
  • Experience with change control
  • Effective technical writing and verbal communication skills
  • Knowledge of non-conformances, root cause investigations, corrective and preventative actions

Nice to have

  • Medical Device or Pharmaceutical Industry experience
  • Experience in medical device IQ, OQ, and PQ process validation
  • Experience in Quality Auditing and notified body inspections
  • Software Quality Engineer certification (CSQE) or Quality Engineer certification (CQE)

What the JD emphasized

  • regulated environment
  • FDA and European medical device regulations
  • GAMP5 and SDLC
  • Part 11 regulations