Quality Assurance Associate III

Posted on Oct 3, 2024 by Eurofins USA BioPharma Services
Columbia, MO
Research
Immediate Start
Annual Salary
Full-Time
Job Description

Job Summary: Eurofins BPT Columbia is seeking a Quality Assurance Associate III to join their team in Columbia, MO on a full-time basis. This individual will provide assistance in improving quality processes and ensuring compliance with GMP and/or GLP systems and regulations.

Essential Job Duties:

Applies GMP/GLP in all areas of responsibility, as appropriate

Meets all quality and productivity metrics and demonstrates strong teamwork and collaboration

Reviews and approves/rejects completed client laboratory reports and like records for accuracy, traceability, and completeness.

Evaluates addressed deficiencies for clarification and for potential impact on compliance status.

Works with staff to correct any noted deficiencies/inconsistencies.

Implementation and monitoring of quality systems and procedures (e.g. CAPA, change controls, trainings, etc.)

Reviews protocols, procedures, data, reports, and other documents to ensure accordance with specified regulatory requirements, protocol, and/or project plan, methods, and SOPs.

Keeps supervisor informed of significant issues or developments identified during quality assurance activities.

Performs internal, external, and quality audits (cGMP, GLP, DEA, etc.)

Develops content and format of training materials for cGMP and/or GLP and QA.

Executes training for new and existing employees.

Conducts all activities in a safe and efficient manner

Performs other duties as assigned

Reference: 203189027

https://jobs.careeraddict.com/post/95758924

Quality Assurance Associate III

Posted on Oct 3, 2024 by Eurofins USA BioPharma Services

Columbia, MO
Research
Immediate Start
Annual Salary
Full-Time
Job Description

Job Summary: Eurofins BPT Columbia is seeking a Quality Assurance Associate III to join their team in Columbia, MO on a full-time basis. This individual will provide assistance in improving quality processes and ensuring compliance with GMP and/or GLP systems and regulations.

Essential Job Duties:

Applies GMP/GLP in all areas of responsibility, as appropriate

Meets all quality and productivity metrics and demonstrates strong teamwork and collaboration

Reviews and approves/rejects completed client laboratory reports and like records for accuracy, traceability, and completeness.

Evaluates addressed deficiencies for clarification and for potential impact on compliance status.

Works with staff to correct any noted deficiencies/inconsistencies.

Implementation and monitoring of quality systems and procedures (e.g. CAPA, change controls, trainings, etc.)

Reviews protocols, procedures, data, reports, and other documents to ensure accordance with specified regulatory requirements, protocol, and/or project plan, methods, and SOPs.

Keeps supervisor informed of significant issues or developments identified during quality assurance activities.

Performs internal, external, and quality audits (cGMP, GLP, DEA, etc.)

Develops content and format of training materials for cGMP and/or GLP and QA.

Executes training for new and existing employees.

Conducts all activities in a safe and efficient manner

Performs other duties as assigned

Reference: 203189027

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