Quality Assurance Inspector
Job in
Pittsburgh, Allegheny County, Pennsylvania, 15289, USA
Listed on 2026-07-18
Listing for:
KVK Tech, Inc.
Full Time
position Listed on 2026-07-18
Job specializations:
-
Quality Assurance - QA/QC
Quality Control - QC Analysts/Managers, Production QC/QA, Regulatory Compliance Specialist
Job Description & How to Apply Below
The QA Inspector is responsible for performing in-process and final inspections on the production and packaging floors 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.
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.
- 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.
- 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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