QA Manufacturing Supervisor

San Francisco  ‐ Onsite
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Keywords

Description

We are urgently seeking a QA Manager to come in and oversee all CMOs for a large pharmaceutical company. This position will report into the Sr. Director of Quality Operations, but still possess an extremely high level of individual responsibility. We are looking for an experienced QA professional who can maintain and establish QA systems, processes, procedures and controls in order to maintain the product quality for the future. This manager will also be responsible for taking the lead on all GMP audits.

Key Responsibilities:
  • Quality oversight of contract manufacturing organizations.
  • Quality representative for FDA investigations related to product compliance. Includes oversight and evaluation of discrepancies and CAPAs.
  • Lead all GMP audits and oversee contract auditing team
  • Manages all documents received from CMOs through document change control and archival process, as required by internal procedures.
  • Coordinate annual product quality reviews with suppliers and internally as required.
  • Initiate updates and creation of new SOPs as required.


Skills Required:
  • 10+ years working in Quality Assurance for an FDA regulated Pharmaceutical or Biotech company.
  • Highly extensive knowledge of cGMP standards and quality systems.
  • Must posses Quality management and leadership skills.
  • 20% travel required


If you believe that you have the skills and can fulfill these responsibilities, please apply and I will reach out to you shortly.

To find out more about Real please visit www.realstaffing.com
Start date
04/2014
From
Real Staffing
Published at
13.04.2014
Project ID:
694876
Contract type
Permanent
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