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Nutramax Manufacturing

37 Nutramax Manufacturing Jobs Hiring Near You

Nutramax Laboratories

QA Specialist

Lancaster, SC · On-site

... 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 ...

Nutramax Laboratories

Microbiologist I

Lancaster, SC · On-site

$20.75 - $27.25/hr

The QCM I will follow Current Good Manufacturing Practice (cGMP) documentation guidelines to record ... The QCM will perform evaluation/ validation testing on Nutramax Laboratories, Inc. finished ...

Nutramax Laboratories

Microbiologist I

Lancaster, SC · On-site

$20.75 - $27.25/hr

The QCM I will follow Current Good Manufacturing Practice (cGMP) documentation guidelines to record ... The QCM will perform evaluation/ validation testing on Nutramax Laboratories, Inc. finished ...

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Infographic showing various job openings at Nutramax Manufacturing in the United States as of August 2026, with employment types broken down into 50% Full Time, and 50% Nights. Highlights an 100% Physical job distribution.

Quality Assurance Auditor

Nutramax Manufacturing

Lancaster, SC • On-site

Full-time

This job post has expired today. Applications are no longer accepted.

Job description

Description

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, drug screen (subject to applicable law). 


Summary of the Position 

The Quality Assurance Auditor reports to the Supplier Quality and Compliance Manager. This role is responsible for developing and maintaining a strong Internal Compliance program ensuring compliance to applicable regulations. The QAA is required to perform internal and external audits, prioritize audit schedules and corrective actions to the findings identified. 

Roles and Responsibilities

  • Manage audit planning, scheduling, and execute internal and external audits for Nutramax Laboratories to assess compliance to the regulations.
  • Audit external suppliers (CMO's) and maintain the vendor qualification program including the Approved Vendor List in Qualityze
  • Manage external vendor(s) responsible for international audits
  • Manage the Nutramax supplier corrective action request program (SCAR).
  • Manage all documents relating to audits, vendors, and suppliers in a QMS (Qualityze)
  • Determine the level of risk of findings identified and follow up on corrective actions ensuring they address the short-term correction as well as the preventive action of the finding.
  • Develop and implement a performance tracking system and reporting of departmental compliance.
  • Prioritize work to ensure that audits and reports are completed in a timely manner. Support implementation of CAPA program where necessary.
  • Train and assist internal departments to understand and comply with Quality and Compliance expectations.
  • Assess internal audit process by identifying and prioritizing areas of the business where there is a risk of non-compliance and assist in development and/or execute processes or policies to reduce that risk.
  • Support training and readiness for regulatory inspections.
  • Provide support to other Quality Assurance team members.
  • Report  audit metrics to Quality Assurance and department management.
  • Communicate effectively with all levels of the organization and departments within the organization and function within a team environment.
  • Understand the roles and responsibilities of the Contract Manufacturing Organizations and provide Quality Assurance support for product development, investigations, and CAPAs as required. 
  • Familiar with QA functions in SAP.
  • Perform other assigned duties as may be required in meeting Quality Assurance and company objectives.


Requirements

Minimum Requirements 

  • Must have a minimum of 5 years of Quality Assurance auditing experience in cGMP environment with a minimum of 5 years of external vendor/ supplier compliance auditing experience within an FDA regulated industry. 
  • Knowledge of the Regulations 21CFR Part(s) 210, 211, 507 as well as the Dietary Supplement Regulations 21 CFR 111 is required.
  • ASQ Certified Auditor (CQA) Certification is preferred.
  • Must be proficient in Computer Software applications including MS office suite.
  • Must be able to stand, walk, push, and pull in a variety of environments including a Manufacturing and clean rooms. 
  • Must have the ability to wear all required Personal Protective Equipment (PPE) based on the auditing environment. 
  • Must be able to travel 20 - 30% for domestic audits, (International travel may be needed per quality management).


Education and Experience:  

  • B.A. or B.S. in Science or Technical field required.

Supervisory Responsibilities:  None

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