Quality Specialist- 7673

Quality Specialist- Simply Biotech

OVERVIEW

Immediate opening for a Quality Specialist in San Diego, CA who possesses:

• Experience with Quality Auditing
• Batch Record experience
• Familiar with GMP

Key Attributes & Skills

• Previous quality experience in GMP environment
• Knowledge of CAPA (Corrective & Preventative Actions)
• Quality Audit experience
• Ability to work in fast-paced environment and work with minimal supervision

Email resumes to sdinfo@simplybiotech.com or call 858.800.3050

FULL DESCRIPTION:

Simply Biotech has partnered with a leader in the research, development, and manufacturing of innovative cell therapies seeking an experienced Quality Specialist.  Our client offers a challenging and rewarding career that will allow you to handle the complete Quality process from start to finish.

The Quality Specialist will manage lab investigations and oversee all steps of receiving records for release of incoming materials, environmental monitoring, and reviewing of Quality Records.  If you enjoy handling many tasks and are ready to jump in and hit the ground running, please continue reading for more details!

The selected candidate will be responsible for the following:

• Working with batch records and ensuring compliance with FDA regulations
• Diligent record keeping and document management to ensure preparedness for any possible audits by FDA and/or internal committees
• Investigate nonconformities / discrepancies and make assessment to identify root cause
• Determine corrective action to eliminate causes of nonconformities; take action to eliminate cause

For immediate and confidential consideration, please email your resume to sdinfo@simplybiotech.com or call 858.800.3050

More information can be found at www.simplybiotech.com

Simply Biotech has been recognized as a Best Place to Work 2016!

Company Description

Simply Biotech specializes in recruiting exclusively for the biotech community.

Work location: San Diego, CA