QA Specialist: GMP Quality & Process Improvement

Nutramax Laboratories, Inc.; Lancaster (SC); On-site; USD 55,000 - 85,000; Full time

Job summary

Nutramax Laboratories, Inc. is seeking a Quality Assurance Specialist to support on-site QA in Manufacturing and Packaging and related GMP functions. The role emphasizes process improvements, non-conformance investigations, and collaboration with the QA department and CMO activities.

Ideal candidates have strong cGMP knowledge, attention to detail, and the ability to work independently or in a team. Familiarity with SAP and QA-related software is a plus, with a focus on documentation and

Qualifications

• Requires cGMP knowledge in a dietary supplement or pharmaceutical environment.
• Strong interpersonal skills and the ability to interact with all staff levels.
• Attention to detail with process analytical skills; ability to learn Nutramax procedures.

Responsibilities

• Provide In-process Review and Training to production operators.
• Assist with trending and developing QA metrics through the QA department.
• Review and release of CMO batch records and assist with in-house batch release.
• Perform Non-conformance investigations and monitor NCRs/CAPAs.
• Create/Revise SOPs, batch records, and other GMP documentation.
• Support QA and Manufacturing through process improvements and cross-function collaboration.
• Communicate effectively with other departments and work within a team environment.

Skills

cGMP knowledge

Interpersonal skills

Critical thinking

Team collaboration

Attention to detail

Independent worker

Documentation review

Communication

Education

High School Diploma or GED

Tools

SAP

Qualityze

LIMBS

Excel

Word

Outlook

Job description

Nutramax Laboratories, Inc. is seeking a Quality Assurance Specialist to support on-site QA in Manufacturing and Packaging and related GMP functions. The role emphasizes process improvements, non-conformance investigations, and collaboration with the QA department and CMO activities.

Ideal candidates have strong cGMP knowledge, attention to detail, and the ability to work independently or in a team. Familiarity with SAP and QA-related software is a plus, with a focus on documentation and