Apply and promote best-practice use of internal Quality Management System to
ensure regulatory compliance.
Lead validation efforts for GxP-regulated computerized systems used acrossthe
organization including quality, manufacturing, clinical, business systems, etc.
Develop and improve non-product software validation procedures, templates,
and maintain the software master validation plan.
Write validation plans, protocols, reports for non-product computer software
validation.
Review and approve validation plans, protocols, executed validation protocols
and summary reports.
Collaborate with software owners to write intended uses, user requirements, risk
analysis, and system requirements.
Evaluate software changes to determine if re-validation is required.
Manage validation timelines and deliverables to drive completion of software
validation activities.
Responsible for other duties as assigned which may include, but is not limited to
supporting processes within training, document control, audits, and CAPA.
Support and improve change control processes related to validated systems.
Ensure validation aligns with internal procedures and external regulatory
expectations, including GAMP 5 and 21 CFR Part 11.
Collaborate with IT, QA, Engineering, Manufacturing, Clinical, and external
vendors to ensure validation activities are executed effectively, efficiently and
meet regulatory requirements.
Mentor junior staff and cross-functional team members on computer software
validation best practices and data integrity principles.
Qualifications and Experience :
Bachelor’s in engineering, Computer Science, Information Technology, or Life
Sciences, etc.
Minimum of 6 years of Engineering work experience with a BS in the medical
device or similarly regulated industry
Preferred 3 years’ experience in a software validation function in a regulated
environment
Deep understanding of GAMP 5, 21 CFR Part 11, Annex 11, and ISO 13485.
Experience implementing and validating systems in a cloud / SaaS environment.
Experienced in Microsoft Office, Google Suite, Jama, and ePLM / eQMS systems.
Must be a self-starter, team builder, and excellent in verbal and written
communication.
Preferred Certifications : GAMP Practitioner, PMP, ASQ-CQA, etc.
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Validation Engineer • San Mateo, CA, United States
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