Quality Auditor - Pharmaceutical

Posted 10 Days Ago
Be an Early Applicant
Columbus, OH
Entry level
Consulting
The Role
Performing Quality System and GMP compliance audits of Suppliers in Pharmaceutical and Cosmetics manufacturing industries. Requires strong knowledge of GMP regulations, quality standards, and audit types. Must have excellent English communication skills and be willing to travel to supplier locations on a contract basis.
Summary Generated by Built In

SQA Services is a leading Quality Assurance and Supply Chain consultancy firm. SQA manages Supplier Audit and Supplier Development programs for customers in many industries including Pharmaceutical, Medical Device, Automotive, Aerospace, and Electronics manufacturing. Clients leverage SQA’s network of Quality Professionals in more than 50 countries as an extension of their own Supplier Quality teams.

 

Job Title: Quality Auditor / GMP Auditor

Description and Requirements:

Auditor will be responsible for performing Quality System and GMP compliance Audits of Suppliers to the Pharmaceutical or Cosmetics manufacturing industries. The overall goal of SQA’s Supplier Audit programs is to mitigate risk across our customers’ supply chains. Supplier Audits typically last 1-3 days on-site not including audit report generation.

 

The right candidate must be familiar with pharmaceutical or related manufacturing processes and be thoroughly familiar with GMP/cGMP regulations (e.g. FDA cGMPs, ICH, IPEC, etc…). 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

· FDA Regulations:

o 21 CFR part 210/211 (current Good Manufacturing Practice for Pharmaceuticals)

o 21 CFR part 820 (Medical Devices)

o 21 CFR part 11 (Electronic Records)

o 21 CFR part 58 (Good Laboratory Practices)

· Eudralex vol. 4

· Canada GMP

· ICH Q7 – Active Pharmaceutical Ingredients / APIs

· IPEC Excipient GMPs

· IPEC GDP

· ISO 13485

· ISO 17025

· ISO 9001

· WHO Guidelines

· Other international GMP guidelines

 

The Quality Auditor must have strong English communication skills, both written and verbal. Auditor will work directly with SQA Services headquarters personnel in Los Angeles, USA, but can be located anywhere in the world.

 

This job is done on a contract basis where you are paid per audit. This position requires travel to various supplier locations. All travel and expenses are covered by SQA Services with approval.

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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