Senior QA Specialist – GMP, ISO 13485 & Audits
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Quality Assurance - QA/QC
Job Description & How to Apply Below
LGC Group is seeking a Quality Assurance Specialist in the United States to provide advanced QA support across manufacturing and regulatory affairs. The role reviews quality records, leads investigations, supports internal and external audits, and improves processes in line with ISO 9001 and ISO 13485.
Responsibilities include approving release records, investigating quality issues, initiating CAPAs, and tracking risk mitigation. Strong collaboration with cross-functional teams is essential.
Consider building your career as a Senior QA Specialist – GMP, ISO 13485 & Audits at LGC Group.
We aim to respond to suitable candidates as soon as possible.
Full responsibilities and requirements are described in the listing above.
Learn more about the Senior QA Specialist – GMP, ISO 13485 & Audits role in the description above.
We appreciate your interest in this position.
Position Requirements
10+ Years work experience(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
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