Sign upLog in

QA Specialist

Integrated Resources, Inc

Foster City, California

Apply
JOB DETAILS
JOB TYPE
Contractor
SKILLS
Auditing, Contract Manufacturing, Corrective Action, Corrective and Preventative Action (CAPA) Systems, Current Good Manufacturing Practice (cGMP), Document Management, Documentation, Employee Retention, Environmental Monitoring, External Audit, GLP (Good Laboratory Practices), GMP (Good Manufacturing Practices), Identify Issues, Maintain Compliance, Manufacturing, Organizational Skills, Problem Solving Skills, Product Reviews, Quality Assurance, Quality Control, Regulatory Compliance, Regulatory Requirements, Research & Development (R&D), Standard Operating Procedures (SOP), Standards Development, Startup, Statistical Process Control, Statistics, Talent Management
LOCATION
Foster City, California
POSTED
3 days ago
QA SpecialistIntegrated Resources, Inc., is led by a seasoned team with combined decades in the industry. We deliver strategic workforce solutions that help you manage your talent and business more efficiently and effectively. Since launching in 1996, IRI has attracted, assembled and retained key employees who are experts in their fields. This has helped us expand into new sectors and steadily grow.Job DescriptionPerforms a wide variety of activities to ensure compliance with applicable regulatory requirements.Participates in developing Standard Operating Procedures to ensure quality objectives are met.Maintains programs and processes to ensure high quality products and compliance with current Good Manufacturing Practices (GMPs) and Good Laboratory Practices (GLPs).Reviews routine manufacturing, environmental monitoring and quality control data for in-process and finished products.Develops solutions to more complex problems and identifies deviations from accepted practice and evaluates impact assessment as required.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 facilitate external audits/inspection processes, supporting implementation of corrective actions as agreed.Participates in the writing of annual product reviews.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 routine checkpoints for new products and processes.May assist with compliance audits as required.Interfaces with contract manufacturers to address documentation and compliance issues.Writes and/or implements changes to controlled documents (e.g., SOPs, specifications, methods, etc.) as needed.Normally receives no instruction on routine work, general instructions on new assignmentQualificationsMin 7 years of experienceNo necessarily all in QAOperations and some QA is goodExperience with CAPA

About the Company

I

Integrated Resources, Inc