Remote Quality Engineering & Compliance Consultant - 80- 110 hour

We are sharing a specialised part-time consulting opportunity for professionals experienced in quality engineering, regulated-industry compliance, audit preparation, CAPA workflows, verification and validation, and structured quality documentation processes.

This role supports current and upcoming remote consulting opportunities focused on structured quality engineering review, compliance documentation, audit response analysis, non-conformance review, validation protocol assessment, and high-quality project execution. Selected professionals will apply their quality and compliance expertise to review realistic regulated-industry scenarios, evaluate documentation requirements, prepare structured written outputs, and support accurate, evidence-based quality workflow tasks.

Key Responsibilities

Professionals in this role may contribute to:

Non-Conformance & CAPA Review

• Review quality scenarios involving non-conformance reports, CAPA documentation, containment actions, root cause analysis, corrective actions, and preventive actions
• Evaluate NCRs and CAPAs against required fields, documented evidence, process requirements, and defined quality criteria
• Support structured review of investigation records, deviation documentation, containment plans, and closure materials
• Identify missing information, documentation gaps, expected corrective steps, and quality process requirements

Audit Preparation & Regulatory Documentation

• Review audit preparation scenarios involving ISO, FDA, automotive, aerospace, medical device, pharmaceutical, or other regulated-industry requirements
• Evaluate audit responses against specific clauses, documented evidence, required citations, and compliance expectations
• Support structured review of quality manuals, audit findings, inspection responses, and compliance documentation
• Prepare clear written explanations for quality and compliance decisions based on source materials and defined criteria

Verification, Validation & Quality Protocols

• Review verification and validation scenarios involving inspection protocols, IQ/OQ/PQ documentation, acceptance criteria, test evidence, and pass/fail outcomes
• Evaluate V&V protocols against defined requirements, documented results, and quality standards
• Support structured review of inspection records, validation documentation, risk controls, and test outcomes
• Maintain accuracy, consistency, and professional judgment across submitted work

Ideal Profile

Strong candidates may have:

• 3+ years of experience in quality engineering, compliance, validation, audit preparation, regulatory quali