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Environment:

The client is looking for a Quality Manager that understands the dynamics and challenges of a new sterile manufacturing facility.

Pharmaceutical CSV SME - Biologics Job Duties/Responsibilities:

The candidate must possess in depth knowledge of QA function and be hands on in Current USFDA compliance expectations, applicable to a sterile manufacturing facility. The client ideally wants this person to have experience working in a plant right from the inception of a new facility. Specifically, this individual will be managing functions of IPQA, Microbiology, Sterility, Training, Audits, Systems, QMS Development & Review, CAPA and Change Control. They will have control over day-to-day activities of the QC department within chemical laboratory, microbiology and instrumentation. They should also be familiar with HPLVC, IR, UV, dissolution and apparatus.

Pharmaceutical Equipment Validation Validation Project Manager Required: Head of Quality Assurance Head of Production Pharmaceutical CSV SME - Biologics Pharmaceutical Equipment Validation Validation Project Manager Head of Quality Assurance Head of Production Pharmaceutical CSV SME - Biologics
Associated topics: bacteria, dietetic, healthcare, histotechnologist, medical, nephrology, patient, pharmacology, therapy, trauma

* The salary listed in the header is an estimate based on salary data for similar jobs in the same area. Salary or compensation data found in the job description is accurate.

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