Quality Auditor - Pharmaceutical

SQA is a leading Quality Assurance and Supply Chain solutions firm. SQA manages Supplier Audit and Supplier Development programs for clients in quality-critical industries, including Pharmaceutical, Medical Device, Automotive, Aerospace, and Electronics manufacturing. Clients leverage SQA’s network of Quality Professionals in more than 90 countries as an extension of their own Supplier Quality teams.

Looking for a local candidate.

Description and Requirements:

Auditor will be responsible for performing Quality System and GMP compliance Audits of Suppliers to the healthcare / life science manufacturing industries. The overall goal of SQA’s Supplier Audit programs is to mitigate risk across our client supply chains. Supplier Audits typically last one, two, or three days on-site, not including audit report generation. 

The right candidate must be familiar with pharmaceutical, medical device or related manufacturing processes and be thoroughly familiar with GMP regulations. The auditor must have strong QMS/GMP Auditing experience having conducted many Supplier or External audits throughout his or her career.

Relevant quality standards and audit types include, but are not limited to: 

Seeking a candidate with minimum qualification of EU GDP Auditor.

SQA shall provide services at the level of Senior Quality Auditor. SQA Associates at this level have at least five years’ experience and are deployed based upon their subject matter expertise relative to the manufacturing environment. They possess expert knowledge relating to specific commodities and tools. Depending on the requirements of the program, they may be trained and certified by a recognized industry body to perform quality audits in a specific environment to be audited (e.g. ISO 9001, ICH Q7,Q10), and shall be experienced in the commodity or activity of the auditee (e.g. API, raw materials, sterilization, distribution).