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QA Specialist

IntegratedResourcesINC

Foster City, CA, United States contract

Posted: December 23, 2016

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Quick Summary

Develop and implement software development methodologies and tools to improve the efficiency and effectiveness of the organization's software development process, ensuring that all projects meet the required standards and are delivered on time, within budget and to the satisfaction of stakeholders.

Job Description

Integrated 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.

• Performs 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 assignment

• Min 7 years of experience
• No necessarily all in QA
• Operations and some QA is good
• Experience with CAPA

Feel free to forward my email to your friends/colleagues who might be available. We do offer referral Bonus.

Thank you.

Kind Regards,

Harris Kaushik

Clinical Recruiter

Integrated Resources, Inc.

IT Life Sciences Allied Healthcare CRO

DIRECT # - (732)-844-8715

Gold Seal JCAHO Certified ™ for Health Care Staffing

“INC 5000’s FASTEST GROWING, PRIVATELY HELD COMPANIES” (8th Year in a Row)

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