Specialist QA II Manufacturing Oversight - Boca Raton, FL

The QA Specialist II - Manufacturing Oversight will perform manufacturing oversight activities to ensure compliance with policies and procedures.Oversight activities include real-time manufacturing batch record review review of manufacturing documentation logs charts etc. and res ...

+Job summary · We currently have an exciting opportunity available for a Specialist QA II Manufacturing Oversight in Boca Raton. · +Possess an understanding of processes such as Quality Systems (e.g., Deviations, Corrective and Preventive Action reports {CAPAs}, Change Controls, ...

ADMA Biologics is a biopharmaceutical company committed to creating superior products for immunodeficient patients. We currently have an exciting opportunity available for a Specialist QA II Manufacturing Oversight in Boca Raton. · ...

We currently have an exciting opportunity available for a Specialist QA II Manufacturing Oversight in Boca Raton, FL. · The QA Specialist II - Manufacturing Oversight will perform manufacturing oversight activities to ensure compliance with policies and procedures.Oversight activ ...

We currently have an exciting opportunity available for a Specialist QA II Manufacturing Oversight in Boca Raton. · Possess and understanding of processes such as Quality Systems (e.g., Deviations, Corrective and Preventive Action reports {CAPAs}, Change Controls, and Out of Spec ...

The company ADMA Biologics is looking for a Specialist QA II Manufacturing Oversight in Boca Raton, FL. The candidate will perform manufacturing oversight activities to ensure compliance with policies and procedures. · Possess and understanding of processes such as Quality System ...

We currently have an exciting opportunity available for a Specialist QA II - Manufacturing Oversight in Boca Raton, FL. · The QA Specialist II - Manufacturing Oversight will perform manufacturing oversight activities to ensure compliance with policies and procedures. ...

The Specialist QA II Manufacturing Oversight will perform manufacturing oversight activities to ensure compliance with policies and procedures. · ...

The company is committed to creating superior products for immunodeficient patients at risk for infection. The Specialist QA II - Manufacturing Oversight will perform manufacturing oversight activities to ensure compliance with policies and procedures. · ...

Seeking an experienced QA professional to provide quality oversight for sterile manufacturing operations. · ...

+Provide quality oversight for sterile manufacturing operations with direct support of aseptic vial filling and fill-finish activities. · Provide QA oversight for aseptic vial filling stoppering and capping operations. · Review and approve batch records related to vial filling an ...

The QA Specialist will provide quality oversight for sterile manufacturing operations, · specifically supporting aseptic vial filling and fill-finish activities. · Provide QA oversight for aseptic vial filling, stoppering, and capping operations. · ...

The Quality Assurance Specialist will provide hands-on quality oversight for sterile manufacturing operations, · The role ensures compliance with cGMP FDA regulations and internal quality systems while supporting manufacturing excellence and inspection readiness.Provide QA oversi ...

The In-Process QA Specialist is responsible for providing quality oversight during sterile manufacturing operations to ensure compliance with cGMP standards and regulatory requirements. · B.Pharm or M.Pharm · Minimum 5 years of QA experience in sterile injectable manufacturing · ...

+h2>Job summary · Lorem ipsum dolor sit amet, · consectetur adipiscing elit. · +ul>+li>In-process QA monitoring for sterile products · Line clearance activitiesQualifications · +ul>+li>B.Pharm / M.Pharm · Experience in sterile injectable production QA </li <+/ul,+valid_job:1} ...

The In-Process QA Specialist is responsible for ensuring quality oversight during sterile injectable manufacturing operations.The role involves real-time monitoring of production activities, documentation review, and ensuring compliance with cGMP and regulatory requirements to ma ...

Job Description · Performs laboratory tests including routine and specialized testing for contracts and customers in compliance with GMP and established procedures. Perform instument calibration or qualification according to written procedures. Perform instrument troubleshootin ...

We currently have an exciting opportunity available for an Associate Director, Quality Engineering in Boca Raton, · FL. If you are looking for a dynamic, innovative, growing company in the biopharmaceutical industry that is committed to excellence and integrity, · then consider A ...

Performs laboratory tests including routine and specialized testing for contracts and customers in compliance with GMP and established procedures. · ...

We currently have an exciting opportunity available for an Associate Director, Quality Engineering in Boca Raton, · FL. · The Associate Director will collaborate cross-functionally with Manufacturing, · Facilities, · Engineering, · Validation, · and Quality Assurance teams to mai ...