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Associate Director Quality Assurance

  • ... Posted on: Feb 23, 2026
  • ... Germer International - Pharmaceutical Recruiting
  • ... Blue Bell, Pennsylvania
  • ... Salary: Not Available
  • ... Full-time

Associate Director Quality Assurance   

Job Title :

Associate Director Quality Assurance

Job Type :

Full-time

Job Location :

Blue Bell Pennsylvania United States

Remote :

No

Jobcon Logo Job Description :

Our client, a well-established, pharmaceutical organization is hiring an Associate Director of Quality Assurance. This role will be a leader in an organization that continues to grow and establish themselves as a global leader. Responsibilities include, but are not limited to:Support the continuous improvement of manufacturing quality systems and processes.Provide QA oversight for all manufacturing operationsReview and approve manufacturing batch records, line clearance documentation, and associated QA forms.Train and mentor QA personnel and manufacturing operators on quality-related topics.Oversee and (commonly) author investigation of manufacturing deviations, non-conformances, and out-of-specification (OOS) results.The ideal candidate would have 8–10 years of progressive experience in pharmaceutical manufacturing quality assurance or quality systems with a degree in Chemistry, Pharmacy, Biology, or related scientific discipline and a QA or Quality Management Certification (e.g., ASQ CQA, CQE)This role does require relocation to the facility located in the midwest.

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Jobcon Logo Position Details

Posted:

Feb 23, 2026

Reference Number:

10440_4368845323

Employment:

Full-time

Salary:

Not Available

City:

Blue Bell

Job Origin:

APPCAST_CPC

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Our client, a well-established, pharmaceutical organization is hiring an Associate Director of Quality Assurance. This role will be a leader in an organization that continues to grow and establish themselves as a global leader. Responsibilities include, but are not limited to:Support the continuous improvement of manufacturing quality systems and processes.Provide QA oversight for all manufacturing operationsReview and approve manufacturing batch records, line clearance documentation, and associated QA forms.Train and mentor QA personnel and manufacturing operators on quality-related topics.Oversee and (commonly) author investigation of manufacturing deviations, non-conformances, and out-of-specification (OOS) results.The ideal candidate would have 8–10 years of progressive experience in pharmaceutical manufacturing quality assurance or quality systems with a degree in Chemistry, Pharmacy, Biology, or related scientific discipline and a QA or Quality Management Certification (e.g., ASQ CQA, CQE)This role does require relocation to the facility located in the midwest.

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