Specialist

Quality Assurance

Location: Novato, CA

Pay Rate: $25/hr.

Duration: 12 months (Potential for Full-Time Employment Conversion)

On behalf of our global pharmaceutical client dedicated to pioneering first-in-class and best-in-class therapeutics for patients facing serious and life-threatening rare genetic diseases. We are seeking for a Quality Assurance Specialist that will provide oversight of one or more portions of operations in the manufacturing process.

Responsibilities:

Develop Direct observation of manufacturing operation for adherence to GMP.

Review of GMP documentation from manufacturing and/ or QC, which can include logbooks, batch records and test records.

Issuance of Production Batch Record to Manufacturing

Scanning and archiving executed production batch records.

Ensure manufacturing and QC adherence to company policies/procedures, regulatory licenses, industry standards, and GMP regulations.

Working knowledge of United States and European regulatory requirements, guidelines, and recommendations a plus.

Revise QA related procedures as needed.

Education & Experience:

Bachelor's degree in biology, Biochemistry, Chemistry, or related Science degree.

1 year of hands on experience. Preferably already in a fast paced setting within QA regulations.

To apply for this opportunity, please submit your resume in Word or PDF format.