Full-Time
Quality Auditor
Pharmaceutical
Posted on 4/18/2024
Global supplier quality services and data
Mid
Columbus, OH, USA
- Familiarity with pharmaceutical or related manufacturing processes
- Thorough knowledge of GMP/cGMP regulations (e.g. FDA cGMPs, ICH, IPEC, etc.)
- Strong QMS/GMP Auditing experience
- Experience in conducting Supplier or External audits
- Knowledge of FDA Regulations, Eudralex, Canada GMP, ICH Q7, IPEC Excipient GMPs, IPEC GDP, ISO standards, WHO Guidelines, and other international GMP guidelines
- Strong English communication skills
- Performing Quality System and GMP compliance Audits of Suppliers in Pharmaceutical or Cosmetics manufacturing industries
- Mitigating risk across customers' supply chains through Supplier Audit programs
- Working directly with SQA Services headquarters personnel in Los Angeles, USA
- Traveling to various supplier locations for 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