What are the responsibilities and job description for the QA Monitor – 2nd Shift position at KVK Tech, Inc.?
KVK Tech is seeking a detail-oriented QA Monitor to join our team in Newtown, PA.
The QA Monitor plays a critical role in ensuring that all cleaning, sanitation, and line clearance activities are performed in strict alignment with cGMP, internal SOPs, and FDA expectations. This position provides continuous on-floor QA oversight to verify equipment readiness, prevent cross-contamination risks, and reinforce a culture of compliance, data integrity, and operational excellence. The ideal candidate will demonstrate strong attention to detail, comfort working in a regulated manufacturing environment, and the ability to collaborate closely with Production, QA, and Facilities teams.
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 Monitor plays a critical role in ensuring that all cleaning, sanitation, and line clearance activities are performed in strict alignment with cGMP, internal SOPs, and FDA expectations. This position provides continuous on-floor QA oversight to verify equipment readiness, prevent cross-contamination risks, and reinforce a culture of compliance, data integrity, and operational excellence. The ideal candidate will demonstrate strong attention to detail, comfort working in a regulated manufacturing environment, and the ability to collaborate closely with Production, QA, and Facilities teams.
This position’s responsibilities will include, but not be limited to the following:
- Perform independent visual verification of room, equipment, and utensil cleaning prior to use and document results on approved QA monitoring forms.
- Verify that cleaning logs, line clearance forms, and housekeeping records are completed accurately, legibly, and in accordance with cGMP and SOP requirements.
- Conduct routine on-floor monitoring of cleaning and sanitation practices to ensure proper methods, detergent usage, and equipment labeling are followed.
- Inspect and confirm compliance with “Cleaned” and “To Be Cleaned” status tags across manufacturing and packaging areas.
- Observe line clearance activities to ensure complete removal of prior product, components, and documents before batch startup.
- Report, document, and escalate any nonconformance, residue, or GMP deviation identified during monitoring.
- High School Diploma or equivalent required; Associate degree in Life Sciences or a related technical field preferred.
- 0–2 years of experience in a cGMP pharmaceutical or manufacturing environment preferred; experience with cleaning, sanitation, or QA monitoring is a plus.
- Working knowledge of cGMP cleaning and line clearance requirements.
- Ability to interpret, complete, and review QA and cleaning documentation with accuracy and attention to detail.
- Strong observational skills with the ability to identify residue, labeling discrepancies, or noncompliant cleaning practices.
- 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
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