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QC Inspector - 2nd SHIFT at PharmaLink, LLC
Seminole, Florida, United States -
Full Time

Start Date

Immediate

Expiry Date

07 Jan, 26

Salary

0.0

Posted On

10 Oct, 25

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

SOP Validation, Documentation Verification, Audit Findings, Process Improvement, Equipment Monitoring, Calibration Requirements, Nonconformance Reporting, Quality Improvement, Supplier Audits, GDP/GMP Knowledge, Regulatory Standards, Communication Skills, Organizational Skills, Attention to Detail, Warehouse Operations, Team Player

Industry

Pharmaceutical Manufacturing

Description
Description DUTIES AND RESPONSIBILITIES: Perform SOP validation audits. Hands-on end process product and documentation verification audits. Properly document all audit findings timely and accurately. Suggest new SOPs and revisions to current SOPs based on audit results. Propose process improvement ideas to the Business Model to the QA Inspector II based on audit results. Monitor the use of equipment to ensure it is safe and accurate and notify area management of need to discard equipment that does not meet specified requirements. Keep measurement equipment operating accurately by following calibration requirements and notify area management of need for repairs. Report nonconformance/deviation issues to QA Inspector II. Continually identify areas of opportunity to improve efficiency and effectiveness. Advocate for quality improvement throughout the organization. May be required to participate in external supplier audits. Requirements JOB REQUIREMENTS / QUALIFICATIONS 2-3 years’ experience working in a GDP/GMP or ISO environment Maintain knowledge of quality and regulatory standards relevant to the position. Excellent verbal and written communication skills. Excellent organizational skills. Keen attention to detail. General knowledge of quarantine and warehouse operations Ability to meet deadlines and to work independently in a fast-paced environment. Team player. PHYSICAL REQUIREMENTS Ability to walk or stand 85% of the workday. DESIRED KNOWLEDGE/SKILLS GMP Requirements
Responsibilities
The QC Inspector is responsible for performing validation audits and verifying product documentation. They will also suggest improvements and monitor equipment safety and accuracy.