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Quality Assurance Core 3

In Missouri / United States

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Quality Assurance Core 3   

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JOB TITLE:

Quality Assurance Core 3

JOB TYPE:

JOB SKILLS:

JOB LOCATION:

St. Louis Missouri / United States

JOB DESCRIPTION:

Roles that are responsible for the analysis, development, and operation of quality and risk management systems. Activities include developing standards for quality, documentation and processes as well as continuous improvement and preventive activities. Conducts analytics to ensure that the company's products are according to defined quality standards.
IMPACT: Impacts the effectiveness of own work team through quality of services or information provided; typically acts as an informal resource for less experienced colleagues.
COMPLEXITY: Identifies key issues and patterns and spots new, less obvious solutions.
ACCOUNTABILITY/ INDEPENDENCE: Accountable for quality of own work; provides solutions to problems based on practice, existing precedents or procedures; uses discretion to modify work practices and processes to achieve results or improve efficiency. Completes work with a limited degree of supervision.
EXPERIENCE: Requires proficiency through formal and job-related training and considerable on-the-job experience. ORGANIZATION: Typically reports to a Manager role or Project Manager role (for a defined period of time) based on organizational set-up, may have a lead person for day-to-day guidance. High school diploma or equivalent required and 3-5 yrs relevant work experience


• Review batch records for completeness and accuracy based on GMP requirements
• Release of raw materials for internal use within SAP environment
• Write, review, and approve Investigations, OOS, CAPAs and Change Controls
• Ensure acceptable product and process consistency by reviewing executed GMP batch documentation.
• Write, review, and approve Operating Procedures, Manufacturing documents and other QA controlled document under a Quality Managed System (QMS)
• Interact with internal customers and provide support where needed
• Support internal and external audits
• Issue and close out logbooks

Bachelor’s degree with 2-5 years’ experience in GMP manufacturing, validation, QA, QC, or other functional area applicable to the job or an Associate’s degree with 5-7 years applicable GMP experience in the specific QA job function

Position Details

POSTED:

Aug 13, 2022

EMPLOYMENT:

INDUSTRY:

Health Care

SNAPRECRUIT ID:

S1654786808076258

LOCATION:

Missouri / United States

CITY:

St. Louis

Job Origin:

Jobsrus_organic_feed

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Aug 19, 2017 9am-6pm
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Quality Assurance Core 3    Apply

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Roles that are responsible for the analysis, development, and operation of quality and risk management systems. Activities include developing standards for quality, documentation and processes as well as continuous improvement and preventive activities. Conducts analytics to ensure that the company's products are according to defined quality standards.
IMPACT: Impacts the effectiveness of own work team through quality of services or information provided; typically acts as an informal resource for less experienced colleagues.
COMPLEXITY: Identifies key issues and patterns and spots new, less obvious solutions.
ACCOUNTABILITY/ INDEPENDENCE: Accountable for quality of own work; provides solutions to problems based on practice, existing precedents or procedures; uses discretion to modify work practices and processes to achieve results or improve efficiency. Completes work with a limited degree of supervision.
EXPERIENCE: Requires proficiency through formal and job-related training and considerable on-the-job experience. ORGANIZATION: Typically reports to a Manager role or Project Manager role (for a defined period of time) based on organizational set-up, may have a lead person for day-to-day guidance. High school diploma or equivalent required and 3-5 yrs relevant work experience


• Review batch records for completeness and accuracy based on GMP requirements
• Release of raw materials for internal use within SAP environment
• Write, review, and approve Investigations, OOS, CAPAs and Change Controls
• Ensure acceptable product and process consistency by reviewing executed GMP batch documentation.
• Write, review, and approve Operating Procedures, Manufacturing documents and other QA controlled document under a Quality Managed System (QMS)
• Interact with internal customers and provide support where needed
• Support internal and external audits
• Issue and close out logbooks

Bachelor’s degree with 2-5 years’ experience in GMP manufacturing, validation, QA, QC, or other functional area applicable to the job or an Associate’s degree with 5-7 years applicable GMP experience in the specific QA job function


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