Quality Assurance Supervisor, 3rd Shift

Johnson Johnson

Gurabo (PR)

On-site

USD 65,000 - 90,000

Full time

4 days ago
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Job summary

Johnson & Johnson in Gurabo, PR, is seeking a Quality Assurance Supervisor for the 3rd shift to lead the QA Auditors and supervise batch record reviews, disposition activities, and GMP compliance. This role will coordinate with Manufacturing, Packaging, QC, and QA to ensure timely product release and maintain quality standards.

You will drive continuous improvement, support audits, and ensure adherence to cGMPs and company policies, working in a fast-paced manufacturing environment.

Qualifications

  • Bachelor's degree in Science required with a focus in biology, chemistry, or related field.
  • Minimum of four (4) years of experience in the pharmaceuticals environment with knowledge of cGMPs and regulatory inspections.
  • Certified Quality Auditor (CQA) or Green Belt preferred.

Responsibilities

  • Direct supervision of the QA Auditors group and coordinate batch record review, continuous flow processes, quarantine and final disposition.
  • Ensure timely batch record review and disposition for raw materials, intermediates, bulk and finished products per supply chain planning values.
  • Collaborate with Operations, Logistics, Quality Assurance and QC to resolve compliance issues and ensure on-time product delivery.
  • Provide guidance and support to Manufacturing and Packaging Operations to ensure cGMP compliance and adherence to company standards.

Skills

Quality assurance
Regulatory compliance
Auditing

Education

Bachelor's degree in Science

Tools

SAP

Job description

Johnson & Johnson in Gurabo, PR, is seeking a Quality Assurance Supervisor for the 3rd shift to lead the QA Auditors and supervise batch record reviews, disposition activities, and GMP compliance. This role will coordinate with Manufacturing, Packaging, QC, and QA to ensure timely product release and maintain quality standards.

You will drive continuous improvement, support audits, and ensure adherence to cGMPs and company policies, working in a fast-paced manufacturing environment.

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