GMP QA Inspector: Growth & Impact in Pharma

KVK Tech, Inc.; Philadelphia (Philadelphia County); On-site; USD 55,000 - 75,000; Full time

Benefits offered by this job

Competitive compensation with annual 1

Job summary

KVK Tech, Inc. is seeking a QA Inspector to perform in-process and final inspections on the production floor, ensuring products meet quality standards and regulatory requirements.

You will work closely with Production, Engineering and Quality to address issues and maintain rigorous documentation. The role requires 1–3 years of QA/QC in a GMP environment, a high school diploma, and preferred coursework in Life Sciences or Chemistry.

Qualifications

• 1–3 years of QA/QC experience in GMP-regulated manufacturing.
• Knowledge of cGMP and FDA compliance.
• Experience with batch records and document review.

Responsibilities

• Perform in-process inspections and line clearances per SOPs and batch records.
• Monitor manufacturing/packaging to ensure cGMP adherence.
• Inspect raw materials, in-process samples, and finished products for conformance.
• Review batch production and packaging records for accuracy and compliance.
• Document inspection results, deviations, and nonconformances.
• Assist with deviation investigations, CAPAs, and quality events.
• Support audits and continuous improvement initiatives.
• Collaborate with Production, Engineering and Quality to address issues.
• Maintain data integrity and ALCOA+ documentation.

Skills

cGMP knowledge

Inspection techniques

Batch record review

Attention to detail

MS Office

Communication

Time management

Independence

Education

High school diploma

Associate degree coursework (Life Sciences or Chemistry) preferred

Tools

Microsoft Office

Job description

KVK Tech, Inc. is seeking a QA Inspector to perform in-process and final inspections on the production floor, ensuring products meet quality standards and regulatory requirements.

You will work closely with Production, Engineering and Quality to address issues and maintain rigorous documentation. The role requires 1–3 years of QA/QC in a GMP environment, a high school diploma, and preferred coursework in Life Sciences or Chemistry.