What are the responsibilities and job description for the Associate Director Quality Assurance position at Germer International - Pharmaceutical Recruiting?
Our client, a well-established, pharmaceutical organization is hiring an Associate Director of Quality Assurance (Manufacturing). 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 operations
- Review 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.