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.
Job Description
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
Qualifications
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 5 0 0 0's FASTEST GROWING, PRIVATELY HELD COMPANIES" (8th Year in a Row)
Numbers & Facts
Location
Foster City, California
Job Type
Contractor
Skills
Auditingunmatched
Biologyunmatched
Contract Manufacturingunmatched
Contract Research Organization (CRO)unmatched
Corrective Actionunmatched
Corrective and Preventative Action (CAPA) Systemsunmatched
Current Good Manufacturing Practice (cGMP)unmatched
Document Managementunmatched
Documentationunmatched
Employee Retentionunmatched
Environmental Monitoringunmatched
External Auditunmatched
GLP (Good Laboratory Practices)unmatched
GMP (Good Manufacturing Practices)unmatched
Healthcareunmatched
Identify Issuesunmatched
Maintain Complianceunmatched
Manufacturingunmatched
Organizational Skillsunmatched
Problem Solving Skillsunmatched
Product Reviewsunmatched
Quality Assuranceunmatched
Quality Controlunmatched
Regulatory Complianceunmatched
Regulatory Requirementsunmatched
Research & Development (R&D)unmatched
Standard Operating Procedures (SOP)unmatched
Standards Developmentunmatched
Startupunmatched
Statistical Process Controlunmatched
Statisticsunmatched
Talent Managementunmatched
The Joint Commission (TJC)unmatched
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