Quality Auditor - Pharmaceutical

Posted 8 Days Ago
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Senior level
Consulting
The Role
Responsible for performing Quality System and GMP compliance audits of Suppliers in healthcare and life science manufacturing industries. Must have strong QMS/GMP auditing experience and be familiar with pharmaceutical and medical device manufacturing processes. Must meet minimum qualification of EU GDP Auditor. Deployed based on subject matter expertise relative to manufacturing environment.
Summary Generated by Built In

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).

The Company
HQ: Palos Verdes Peninsula, California
350 Employees
On-site Workplace
Year Founded: 1995

What We Do

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 over 50 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: [email protected]

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