Inspect and promote GMP and SOP compliance in an FDA regulated pharmaceutical manufacturing environment, ensuring product integrity, safety and compliance with standards.

Sample and inspect raw materials, in-process and finished goods, packaging and labeling.

Inspect, clear and release manufacturing rooms and packaging lines.

Document procedures, record data and review records for completeness and accuracy to ensure compliance with SOPs and GMPs.

Train and mentor new Quality Assurance Inspectors.

Act as team leader on off-shift when QA supervision may not be present.

Help to identify and present ongoing initiatives for continuous improvements to the organization’s quality process.

5+ years quality experience in a pharmaceutical manufacturing environment.

A BS/BA preferred.

Thorough knowledge of cGMPs, SOPs and FDA regulations.

Ability to work on first or second shift, as well as overtime when required, and able to perform the physical tasks associated with sampling and inspecting.

Must be a highly organized, reliable and detail oriented self-starter able to multi-task and prioritize effectively.

Excellent verbal and written communication skills are required to execute documents and interact successfully with other departments.