Full-Time

Quality Auditor – Senior

Pharmaceutical

Posted on 4/18/2024

SQA Services

SQA Services

201-500 employees

Global supplier quality services and data

Data & Analytics
Industrial & Manufacturing

Senior

Remote in USA

Requirements
  • Familiarity with pharmaceutical, medical device, or related manufacturing processes
  • Strong QMS/GMP Auditing experience
  • Certification for EU MDR, ISO 13485, FDA CFR, ANVISA, TGA, and Japan Regulations
Responsibilities
  • Performing Quality System and GMP compliance Audits of Suppliers
  • Mitigating risk across client supply chains
  • Conducting Supplier or External audits

At SQA Services, Inc., employees are at the forefront of the supplier quality services industry, engaging with the patented STEPQ technology to provide crucial, real-time quality data for quality-critical industries. This role offers a unique opportunity to work within a vast network of experienced professionals in over 50 countries, fostering a rich environment of learning and innovation. The company is committed to maintaining high standards of quality assurance and streamlining global operations, making it an ideal workplace for those passionate about impacting various industries positively through superior quality management systems.

Company Stage

M&A

Total Funding

$282M

Headquarters

Palos Verdes Estates, California

Founded

1995

Growth & Insights
Headcount

6 month growth

3%

1 year growth

5%

2 year growth

11%