Planet Pharma
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https://www.propharmagroup.com
https://www.propharmagroup.com
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Quality Control Senior Associate
Posted: 11/05/2024
2024-11-05
2025-01-04
Employment Type:
Contract
Job Category: Quality and Compliance
Job Number: 615805
Is job remote?: Yes
Country: United States
Job Description
Target PR Range: 27-37/hr
*Depending on experience
Responsibilities: Primary focus is the support and oversight of Quality Management Systems ensuring key requirements and initiatives are implemented, maintained and reviewed in accordance with cGMP regulations. Additional detail responsibilities, accountabilities or decision authorities are defined in procedures to execute assigned task for the role and deployed through assignment of procedure training in the Learning Management System. Responsibilities could include:
• May be responsible for leading and directing the Quality functions for assigned plant(s) or functional area(s)
• Responsible for providing Quality oversight to ensure that systems are executed, according to current Good Manufacturing Practices (cGMP) and other applicable regulations
• Ensures that Quality Management Systems comply with cGMP practices and other applicable regulations
• Provide support for Global Process Owners executing key quality systems processes
• Ensures the Quality unit provides review, approval and tracking of cGMP processes, procedures, assays, documents and records, including nonconformances, CAPAs, change control records and validations. May execute these tasks
• Supports Continual Improvement initiatives, programs and projects
• Ensures that changes that could potentially impact product quality are assessed according to procedures
• Ensures that deviations from established procedures are investigated and documented per procedures
• Collect and analyze Key Process Indicator (KPI) data to assessing process performance and areas of improvement
• Alerts senior management of significant quality, compliance, supply and safety risks
?*CO/NYC candidates might not be considered
*Depending on experience
Responsibilities: Primary focus is the support and oversight of Quality Management Systems ensuring key requirements and initiatives are implemented, maintained and reviewed in accordance with cGMP regulations. Additional detail responsibilities, accountabilities or decision authorities are defined in procedures to execute assigned task for the role and deployed through assignment of procedure training in the Learning Management System. Responsibilities could include:
• May be responsible for leading and directing the Quality functions for assigned plant(s) or functional area(s)
• Responsible for providing Quality oversight to ensure that systems are executed, according to current Good Manufacturing Practices (cGMP) and other applicable regulations
• Ensures that Quality Management Systems comply with cGMP practices and other applicable regulations
• Provide support for Global Process Owners executing key quality systems processes
• Ensures the Quality unit provides review, approval and tracking of cGMP processes, procedures, assays, documents and records, including nonconformances, CAPAs, change control records and validations. May execute these tasks
• Supports Continual Improvement initiatives, programs and projects
• Ensures that changes that could potentially impact product quality are assessed according to procedures
• Ensures that deviations from established procedures are investigated and documented per procedures
• Collect and analyze Key Process Indicator (KPI) data to assessing process performance and areas of improvement
• Alerts senior management of significant quality, compliance, supply and safety risks
?*CO/NYC candidates might not be considered
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