What are the responsibilities and job description for the QA Inspector – 2nd Shift position at KVK Tech, Inc.?
KVK Tech is seeking a dedicated QA Monitor to join our team in Newtown, PA.
The QA Inspector provides real-time oversight on the manufacturing and packaging floors to ensure products meet cGMP requirements, internal quality standards, and applicable regulatory expectations. This role is essential in supporting in-process inspections, documentation review, and deviation identification, helping maintain product quality and compliance across operations. The ideal candidate will be detail-oriented, reliable, and capable of collaborating effectively with cross-functional teams in a fast-paced, regulated environment.
This position’s responsibilities will include, but not be limited to the following:
We encourage you to apply if you feel that you are a match! We look forward to hearing from you.
Apply for this position
The QA Inspector provides real-time oversight on the manufacturing and packaging floors to ensure products meet cGMP requirements, internal quality standards, and applicable regulatory expectations. This role is essential in supporting in-process inspections, documentation review, and deviation identification, helping maintain product quality and compliance across operations. The ideal candidate will be detail-oriented, reliable, and capable of collaborating effectively with cross-functional teams in a fast-paced, regulated environment.
This position’s responsibilities will include, but not be limited to the following:
- Conduct in-process inspections, line clearances, and component verifications according to approved SOPs and batch records.
- Review production, packaging, and cleaning documentation for accuracy, completeness, and cGMP compliance prior to QA approval.
- Monitor manufacturing and packaging activities to ensure adherence to established quality standards and escalate deviations or nonconformances as needed.
- Perform visual and physical inspections of products, components, and labeling to verify conformance with specifications.
- Support deviation investigations, CAPAs, and related quality documentation as directed by QA leadership.
- Ensure data integrity by completing all documentation accurately, contemporaneously, and legibly in alignment with ALCOA principles.
- High school diploma or equivalent required; Associate degree in a science discipline preferred.
- 0–3 years of QA/QC experience in a cGMP pharmaceutical or other regulated manufacturing environment.
- Working knowledge of FDA, cGMP, and documentation compliance expectations.
- Ability to review and interpret batch records, SOPs, and controlled documents with strong attention to detail.
- Effective communication skills and the ability to work both independently and collaboratively on a production floor.
- 401(k) with company match
- Health, vision, and dental Insurance
- Childcare expense reimbursement
- Tuition reimbursement
- Annual bonus eligibility
- Annual merit increases
- Paid Time Off and Flexible Holidays
We encourage you to apply if you feel that you are a match! We look forward to hearing from you.
Apply for this position