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Skills
Auditingunmatched
Clinical Researchunmatched
Corrective Actionunmatched
Corrective and Preventative Action (CAPA) Systemsunmatched
Current Good Manufacturing Practice (cGMP)unmatched
Environmental Monitoringunmatched
GLP (Good Laboratory Practices)unmatched
GMP (Good Manufacturing Practices)unmatched
Information Technology & Information Systemsunmatched
Maintain Complianceunmatched
Manufacturingunmatched
Organizational Skillsunmatched
Product Reviewsunmatched
Quality Assuranceunmatched
Quality Controlunmatched
Regulatory Complianceunmatched
Regulatory Requirementsunmatched
Rehabilitation Nursingunmatched
Research & Development (R&D)unmatched
Standard Operating Procedures (SOP)unmatched
Standards Developmentunmatched
Startupunmatched
Statistical Process Controlunmatched
Statisticsunmatched
Training Program Developmentunmatched
Description
QA SpecialistIntegrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.Job DescriptionJob Title: QA SpecialistLocation: Foster City, 94404Duration: 3-6 MonthsDescriptionPerforms a wide variety of activities to ensure compliance with applicable regulatory requirements.Participates in developing Standard Operating Procedures (SOPs) to ensure quality objectives are met.Maintains routine programs and processes to ensure high quality products and compliance with current Good Manufacturing Practices (GMPs) and Good Laboratory Practices GLPs).Reviews manufacturing, environmental monitoring and quality control data for in-process and finished products.Works directly with operating entities to ensure that inspections, statistical process control analyses and audits are conducted on a continuing basis as specified to enforce requirements and meet specifications.May participate in the writing of annual product reviews and the development of training programs regarding all aspects of producing quality products.May conduct or serve as a lead/coordinator of investigations and corrective and preventive action (CAPA) recommendations related to manufactured products.Works with Research and Development during new product start-ups, and identifies checkpoints for new products and processes.Normally receives very little instruction on routine work, general instructions on new assignments.QualificationsMust have a degree in Science.More than 3 years' experience in Science field.