Remote Quality Auditor - Pharmaceutical

Logo of SQA Services

SQA Services

💵 $286k-$325k
📍Remote - China

Job highlights

Summary

Join our team as a Quality Auditor / GMP Auditor and play a crucial role in mitigating risk across our customers' supply chains by performing Quality System and GMP compliance Audits of Suppliers to the Pharmaceutical or Cosmetics manufacturing industries. As a seasoned auditor, you will leverage your expertise in pharmaceutical or related manufacturing processes and GMP/cGMP regulations to ensure compliance with FDA cGMPs, ICH, IPEC, and other international guidelines.

Requirements

  • Familiar with pharmaceutical or related manufacturing processes
  • Thoroughly familiar with GMP/cGMP regulations (e.g. FDA cGMPs, ICH, IPEC, etc…)
  • Strong QMS/GMP Auditing experience
  • Strong English communication skills (written and verbal)

Responsibilities

  • Perform Quality System and GMP compliance Audits of Suppliers
  • Mitigate risk across customers' supply chains

Benefits

  • Paid per audit on a contract basis ($1,100 - $1,250 a day)
  • Travel to various supplier locations covered by SQA Services with approval

Job description

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:

o21 CFR part 210211 (current Good Manufacturing Practice for Pharmaceuticals)

o ICH Q7

·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.

Auditor local (Shanghai preferred) within country.

$1,100 - $1,250 a day

Share this job:

Disclaimer: Please check that the job is real before you apply. Applying might take you to another website that we don't own. Please be aware that any actions taken during the application process are solely your responsibility, and we bear no responsibility for any outcomes.
Please let SQA Services know you found this job on JobsCollider. Thanks! 🙏