Medivant Healthcare
11440 -Quality Assurance Specialist
Medivant Healthcare, Chandler, Arizona, United States, 85249
Job Summary
Tailstorm Health Inc, a Chandler, AZ based Pharmaceutical Manufacturing Firm, has multiple openings for JOB ID 11440: Quality Assurance Specialist. Base pay range
$56,680.00/yr - $60,000.00/yr Responsibilities
Ensure training compliance for QA Line Operations. Foster teamwork and communication between Quality Assurance, Production, and other support functions to meet plant and department objectives. Involve in manufacturing Assurance (QA) activities, batch Disposition Decision and Document Control Center. Examine Non-Conformance Reports for non-compliance issues, conducting thorough investigation, root cause analysis, and implementing corrective and preventative actions. Plan and execute Gemba walks for compliance improvement. Participate in key meetings such as NCR approach, Market complaint, Major Change control pre-assessment, Quality-Operations, OOS review Board, CAPA review board, Quality Review, and Tier-3 meetings. Review batch records for quality to meet internal targets and commitments, while ensuring product safety and reliability. Manage site Investigations and audit readiness team, contributing to site readiness for regulatory audits and writing audit responses for External/Internal Audits. Qualifications
Bachelor's degree in science, Pharmacy or related field At least 60 months of relevant experience Equal Opportunity Employer. Seniority level
Entry level Employment type
Full-time Job function
Quality Assurance Industries
Pharmaceutical Manufacturing Note: This description excludes unrelated promotional content and focuses on the responsibilities and requirements of the Quality Assurance Specialist role.
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Tailstorm Health Inc, a Chandler, AZ based Pharmaceutical Manufacturing Firm, has multiple openings for JOB ID 11440: Quality Assurance Specialist. Base pay range
$56,680.00/yr - $60,000.00/yr Responsibilities
Ensure training compliance for QA Line Operations. Foster teamwork and communication between Quality Assurance, Production, and other support functions to meet plant and department objectives. Involve in manufacturing Assurance (QA) activities, batch Disposition Decision and Document Control Center. Examine Non-Conformance Reports for non-compliance issues, conducting thorough investigation, root cause analysis, and implementing corrective and preventative actions. Plan and execute Gemba walks for compliance improvement. Participate in key meetings such as NCR approach, Market complaint, Major Change control pre-assessment, Quality-Operations, OOS review Board, CAPA review board, Quality Review, and Tier-3 meetings. Review batch records for quality to meet internal targets and commitments, while ensuring product safety and reliability. Manage site Investigations and audit readiness team, contributing to site readiness for regulatory audits and writing audit responses for External/Internal Audits. Qualifications
Bachelor's degree in science, Pharmacy or related field At least 60 months of relevant experience Equal Opportunity Employer. Seniority level
Entry level Employment type
Full-time Job function
Quality Assurance Industries
Pharmaceutical Manufacturing Note: This description excludes unrelated promotional content and focuses on the responsibilities and requirements of the Quality Assurance Specialist role.
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