Manufacturing Quality Inspector (2nd and 3rd shift)

Nutramax Manufacturing•Lancaster, SC
•Onsite

About The Position

This position provides daily Quality Assurance support for onsite manufacturing and packaging processes. The inspector reviews appropriate production documentation, maintains a consistent presence on the production floor, and remains available to support production in assigned areas. Openings are available on second and third shifts. Employees may be asked to train temporarily on first-shift hours. The role works closely with manufacturing and packaging operators; Quality Assurance and Quality Control staff; Label Issuance and Quality Assurance Document Specialists; Safety, Security, and Environmental Services; Training; Supply Chain; and Product Development. Regular attendance is required. The inspector must follow supervisor instructions and company procedures, communicate effectively across teams, and contribute to a positive work environment. Employment is contingent on successfully passing a pre-employment background check, drug screen (subject to applicable law), and reading comprehension test. The company maintains a zero-tolerance policy for drug use.

Requirements

  • High school diploma or equivalent.
  • Two years of experience in a pharmaceutical, food, dietary supplement manufacturing environment, or another government-regulated environment is preferred.
  • Detail-oriented and team-centered approach.
  • Enthusiasm and a strong work ethic.
  • 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.

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 covering work requirements for 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, or 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.
  • Communicate effectively with the team, supervisors, and other departments, and work collaboratively to promote a positive work environment.
  • Complete required training on SOPs, safety procedures, and cGMPs and keep training current.
  • Maintain regular attendance.
  • Perform other assigned duties and follow verbal and written instructions from a supervisor or designee related to company goals and objectives.
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