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QA Specialist

Job in Lancaster, Lancaster County, South Carolina, 29721, USA
Listing for: Nutramax Laboratories, Inc.
Full Time position
Listed on 2026-08-12
Job specializations:
  • Quality Assurance - QA/QC
    Production QC/QA, Quality Control - QC Analysts/Managers, QA Specialist - Analyst/Manager
Salary/Wage Range or Industry Benchmark: 55000 - 85000 USD Yearly USD 55000.00 85000.00 YEAR
Job Description & How to Apply Below

The Quality Assurance Specialist is responsible for the daily Quality Assurance support in the Manufacturing and Packaging processes on-site as well as all Quality Assurance processes related to CMO. In this role, the QA Specialist will support the Quality Department and Manufacturing through process improvements, non-conformance investigation and other GMP functions; this position requires the QA Specialist to be flexible to support QA and business operations as needed.

Roles and Responsibilities
  • Provide In-process Review and Training to production operators.
  • Understand the roles and responsibilities of the Contract Manufacturing Organizations.
  • Assisting with trending and developing metrics through QA department.
  • Familiarity with QA Functions in SAP.
  • Creating / Revising process changes, SOPs, batch records, and other GMP functions.
  • Perform Non-conformance investigations.
  • Monitor the status of NCRs and CAPAs for completion and reoccurrences.
  • Review and release of CMO batch records and assist with in house batch release.
  • Will assist in the correction of deficiencies found within the documentation review per cGMP, Nutramax SOPs, Contract Manufacturing Organization (SOPs), and Global Regulations criterion.
  • Must be able to effectively communicate with other departments and function within a team environment.
  • Perform other assigned duties as may be required in meeting company objectives.
  • Regular attendance is required.
Requirements
  • Must have working knowledge of cGMP (dietary supplement or pharmaceutical environment)
  • Good interpersonal skills and the ability to interact with all staff levels.
  • Critical thinking skills to learn Nutramax procedures and predict whether proposed changes will be effective.
  • Must be able to work independently and within team environment, according to specific, written and verbal instructions, presented by supervisor or designee.
  • Previous knowledge and understanding of production processes in a cGMP or pharmaceutical environment desired.
  • Attention to detail and some process analytical skills necessary.
  • Regularly required to stand and bend
  • Must be able to use hands and arms to lift and reach
  • Ability to climb up and down stairs
  • Ability to lift, pull and push a minimum of 50 pounds
  • Ability to use both arms to push, pull or lift.
  • Ability to bend and squat
  • Requires the ability to use fractions, decimals, and commercial arithmetic as well as a basic knowledge of grammar, spelling and punctuation.
Education and Experience

This position requires a High School Diploma or GED. 4 years’ experience in the pharmaceutical or dietary supplement manufacturing environment preferred. Auditing experience and troubleshooting is a plus.

Great enthusiasm and hard work ethic is a must. Detail oriented and team centered approach is required. Software skills preferred
- Excel, Word, Outlook, SAP, Qualityze, LIMBS, etc.

Supervisory Responsibilities

None

Nutramax desires to provide a drug-free, healthful, and safe workplace. We hold a zero-tolerance policy for drug use. Employment is contingent upon successfully passing a preemployment background check and drug screen (subject to applicable law).

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