Find & Apply For Quality Control Systems Manager Jobs in Westbury, New York

This position is a second shift position from Tuesday to Saturday, 1:00pm to 9:00pm.

RESPONSIBILITIES

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Batch Record Review & Approval:

Review and approve production batch records to ensure accuracy, completeness, and cGMP compliance.

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Line Clearance Activities:

Perform and document line clearances to ensure production areas are ready for manufacturing and packaging operations.

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Calibration & Equipment Verification:

Verify daily scale calibrations and maintain calibration records in accordance with established procedures.

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In-Process Quality Monitoring:

Conduct in-process quality checks required by the respective SOPs, procedure to ensure product quality standards are met.

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Training & Personnel Development:

Provide GMP, SOP, and quality-related training to support employee competency and compliance.

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Quality Inspections & Audits:

Conduct routine QA inspections and support internal and regulatory audits to maintain compliance.

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Deviation & Investigation Management:

Identify, report, and assist in the investigation of quality issues, deviations, and CAPA activities.

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Operational Support:

Support QA operations, product release activities, and serve as a quality resource for manufacturing personnel.

QUALIFICATIONS

Education

• Bachelor's degree in Pharmaceutical Sciences, Chemistry, Biology, or a related scientific discipline preferred. Experience Minimum 10 years of Quality Assurance experience in pharmaceutical, nutraceutical, or soft gelatin capsule manufacturing. Previous supervisory or leadership experience preferred. Strong knowledge of cGMP regulations, FDA requirements, and pharmaceutical quality systems.

Pay:

From $25.00 per hour Expected hours: No less than 40.0 per week

Benefits:

401(k) 401(k) matching Dental insurance Flexible spending account Health insurance Life insurance Paid time off Vision insurance

Work Location:

In person