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.
Responsibilities
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 elevate 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.
Qualifications
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.
What We Offer
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
KVK Tech is an affirmative action/equal opportunity employer and does not discriminate in hiring or employment on the basis of age, sex, race, color, religion, national origin, gender identity, veteran status, sexual orientation or any other protected status.
We encourage you to apply if you feel that you are a match! We look forward to hearing from you.
Apply for this position
Seniority level
Entry level
Employment type
Full-time
Job function
Quality Assurance
Industries
Pharmaceutical Manufacturing
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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.
Responsibilities
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 elevate 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.
Qualifications
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.
What We Offer
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
KVK Tech is an affirmative action/equal opportunity employer and does not discriminate in hiring or employment on the basis of age, sex, race, color, religion, national origin, gender identity, veteran status, sexual orientation or any other protected status.
We encourage you to apply if you feel that you are a match! We look forward to hearing from you.
Apply for this position
Seniority level
Entry level
Employment type
Full-time
Job function
Quality Assurance
Industries
Pharmaceutical Manufacturing
#J-18808-Ljbffr