SQA Services, Inc.

Www.sqaservices.com

1 Job

415 Employees

About the Company

Welcome to the SQA Services, Inc. home on LinkedIn! Follow us to stay up to date on all things quality - including industry events, news, and ways to get involved with #TeamSQA. Also, keep an eye out for job postings! SQA is always looking for quality professionals and new team members! WHAT IS SQA SERVICES, INC.? SQA provides global supplier quality services for quality-critical industries. With quality, manufacturing, and regulatory experts located in 90+ countries, SQA provides a cost-effective, local supplier presence. Managed, on-demand services include supplier quality audits, supplier remediation, quality engineering, source inspection, corrective action management, and real-time supplier quality data via SQA's world-class STEPQ technology. HOW CAN I GET IN TOUCH WITH SQA? We look forward to connecting with you and discovering how Team SQA can help you and your team reach your quality goals. Contact our team by heading over to http://www.sqaservices.com/contact If you think you or someone you know would be a great fit for our team, please send your resume to our Associate Development team at: recruiting@sqaservices.com

Listed Jobs

Company Name: SQA Services, Inc.
Job Title: Quality Auditor - Pharma/Cell Therapy
Job Description: Job title: Quality Auditor – Pharma / Cell Therapy Role Summary: Independent contract auditor responsible for conducting 1‑2 day Good Manufacturing Practice (GMP) audits of suppliers across the pharmaceutical, medical device, biologics, and cell therapy sectors in France. Deliver audit reports, coordinate schedules, and support client quality assurance. Expectations: * Complete audits within 1‑2 days, including preparation, site visit, and report writing. * Self‑manage compliance with client and regulatory standards, and respond promptly to editors. * Travel regionally as required; flexible to accept or decline assignments. Key Responsibilities: 1. Plan, execute, and close supplier GMP audits at multiple sites. 2. Document findings, recommend corrective actions, and produce audit reports per client specifications. 3. Coordinate audit timelines with clients and internal content teams. 4. Apply regulatory knowledge of ISO, CFR, FDA, and related standards. 5. Communicate audit outcomes clearly to clients and team members. Required Skills: * Minimum 5 years of hands‑on GMP audit experience in pharma, medical device, or biologics. * Strong written and verbal communication; ability to draft concise audit reports. * Conflict de‑escalation and stakeholder management. * Adaptability to new audit software and technologies. * Willingness and ability to travel regionally. Required Education & Certifications: * Bachelor’s degree in Life Sciences, Engineering, or related field preferred. * Industry certifications (e.g., ISO 9001, ISO 13485, GMP, 21 CFR Part 1271) are a plus but not mandatory. ---