What are the responsibilities and job description for the Associate Director Manufacturing position at Germer International - Pharmaceutical Recruiting?
Our client, a well-established, pharmaceutical organization is hiring an Associate Director of Manufacturing (Quality Assurance) with the opportunity to grow in a specialized manufacturing facility. The ideal candidate has:
- Pharmaceutical Manufacturing Experience (in oral solid dosages)
- Supporting manufacturing from the quality perspective
- An understanding of quality on the floor or experience working on the floor
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.
This role does require relocation to the facility located in the Midwest.