Quality Assurance Inspector

KVK Tech, Inc.

Philadelphia (Philadelphia County)

On-site

USD 55,000 - 75,000

Full time

7 days ago
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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

The QA Inspector is responsible for performing in-process and final inspections on the production floor to ensure products meet quality standards and regulatory requirements. This position provides real-time quality oversight, ensuring all operations comply with established procedures, documentation practices, and data integrity expectations.

Key Responsibilities:
  • Perform in-process inspections, component verifications, and line clearances in accordance with approved SOPs and batch records.
  • Monitor manufacturing and packaging operations to ensure adherence to cGMP and internal quality procedures.
  • Inspect raw materials, in-process samples, finished products, and labeling to verify conformance with specifications.
  • Review batch production, cleaning, and packaging records for accuracy, completeness, and compliance prior to QA release.
  • Document inspection results, deviations, and nonconformances accurately and contemporaneously.
  • Assist with deviation investigations, CAPAs, and quality event documentation under QA management direction.
  • Support audits, internal inspections, and continuous improvement initiatives.
  • Collaborate closely with Production, Engineering, and Quality departments to address quality concerns promptly.
  • Maintain data integrity and ensure documentation meets ALCOA+ principles at all times.
  • Perform other related QA responsibilities as required to meet departmental objectives.
What We’re Looking For

Experience: 1–3 years of Quality Assurance or Quality Control experience in a GMP-regulated pharmaceutical, biotechnology, or related manufacturing environment.

Education: High school diploma or equivalent required; Associate degree or coursework in Life Sciences, Chemistry, or a related discipline preferred.

Skills & Knowledge:
  • Strong understanding of current Good Manufacturing Practices (cGMP) and FDA compliance requirements.
  • Knowledge of quality inspection techniques, sampling methods, and documentation review.
  • Experience with batch record review, line clearance, or in-process inspection preferred.
  • High attention to detail with the ability to detect and resolve nonconformances.
  • Proficiency in Microsoft Office (Word, Excel, Outlook) and standard documentation systems.
  • Excellent written and verbal communication skills; able to interact effectively across teams.
  • Strong time-management, organization, and follow-through abilities.
  • Ability to work independently while maintaining a high standard of accuracy and accountability.
What We Offer
  • Competitive compensation with annual performance bonus eligibility
  • Annual merit-based pay increases
  • Automatic enrollment in a 401(k) at 3% pre-tax with 50% company match on the first 6% contributed
  • Comprehensive medical, dental, vision, and life insurance coverage
  • Career growth opportunities
  • Tuition reimbursement for children and childcare expense reimbursement
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