Manufacturing Quality Inspector (2nd and 3rd shift)

Nutramax Laboratories•Lancaster, SC

7d•Onsite

About The Position

This position provides daily Quality Assurance support for on-site manufacturing and packaging operations. The inspector reviews appropriate production documents and maintains a consistent presence on the production floor during the assigned shift to support production processes. Openings are available on second shift (Monday–Friday, 3:15 p.m.–11:30 p.m.) and third shift (Sunday–Thursday, 11:15 p.m.–7:15 a.m.). Short-term training on first-shift hours (Monday–Friday, 7:00 a.m.–3:30 p.m.) may be required. The role works closely with Manufacturing and Packaging Operators; Quality Associates and other QA functions; Safety, Security and Environmental Services; Training; Supply Chain; and Product Development. Employment is contingent upon successfully passing a pre-employment background check, drug screen subject to applicable law, and reading comprehension test.

Requirements

High school diploma or equivalent.
Two years of experience in pharmaceutical, food, dietary supplement manufacturing, or another government-regulated environment is preferred.
Auditing experience and troubleshooting are a plus.
Enthusiasm and a strong work ethic.
Detail-oriented and team-centered approach.
Good computer skills, including general software and Microsoft Office Suite.
Ability to lift 50 pounds.
Must wear Personal Protective Equipment and follow applicable written and verbal instructions and procedures.
Must successfully pass a pre-employment background check, drug screen subject to applicable law, and reading comprehension test.

Nice To Haves

Auditing experience.
Troubleshooting experience.
Experience in pharmaceutical, food, dietary supplement manufacturing, or another government-regulated environment (two years preferred).

Responsibilities

Provide Quality Assurance presence in production areas during packaging lines, manufacturing processes, room clearances, release of cleaned equipment, rooms and areas, and in-process inspections across manufacturing areas.
Provide input during revisions of SOPs to cover work requirements in the assigned facility or process.
Assist with investigations of deviations.
Review the pest control and environmental monitoring system.
Issue labels and other printed materials to operations according to the current production schedule.
Help identify minor and major errors and deficiencies in batch records.
Organize work to achieve daily goals without errors or deficiencies.
Provide input on issues that could affect product quality, safety, and purity.
Assist Quality Assurance management with daily operation of the QA Hold area.
Submit thorough end-of-day reports summarizing daily activities, issues, and actions taken.
Remain current in training on SOPs, safety procedures, and cGMPs.
Attend work regularly, perform other assigned duties, and follow relevant verbal and written instructions from a supervisor or designee.
Communicate effectively with teammates, supervisors, and other departments and contribute to a positive team environment.