Abbott Clinical Quality Manager in Santa Clara, California

At Abbott, we're committed to helping people live their best possible life through the power of health. For more than 125 years, we've brought new products and technologies to the world -- in nutrition, diagnostics, medical devices and branded generic pharmaceuticals -- that create more possibilities for more people at all stages of life. Today, 99,000 of us are working to help people live not just longer, but better, in the more than 150 countries we serve.

  • Manage quality system and manufacturing process audits to applicable standards, regulations and company procedures / policies.

  • Review audit reports that establish the outcome of the audit and detail the non-conformances identified during the audit.

  • Track audit results, including corrective actions, and provide follow-up to these actions, as required.

  • May perform Supplier Audits, as needed.

  • Participate in third party and regulatory agency inspections as a subject matter expert as needed.

  • Manage Supplier CAPAs and non-supplier CAPAs, as needed.

  • Prepare Supplier/CAPA metrics for management review meetings

  • Communicate effectively and efficiently by both written and oral modes.

  • Demonstrate excellent interpersonal skills when dealing with internal and external customers, including Clinical Suppliers/Consultants.

  • Demonstrate the ability to identify, analyze and report opportunities for improvements and execute solutions.

  • Lead project and/or project team, as needed.

An Equal Opportunity Employer

Abbot welcomes and encourages diversity in our workforce.

We provide reasonable accommodation to qualified individuals with disabilities.

To request accommodation, please call 224-667-4913 or email corpjat@abbott.com