KVK Tech, Inc. · 3 weeks ago
QA Monitor (2nd Shift - Entry Level)
Newtown, PA, US
Full-time
Onsite
New Grad, Entry Level
0+ years expKVK Tech is a U.S.-based generic and specialty pharmaceutical manufacturer committed to producing high-quality, FDA-approved medicines. The QA Monitor plays a critical role in maintaining cGMP compliance by overseeing cleaning, sanitation, and line clearance activities across manufacturing and packaging areas.
ManufacturingMedical DevicePharmaceutical
Responsibilities
Visually verify equipment, utensils, and production areas for cleanliness and readiness prior to manufacturing operations
Observe and document cleaning and sanitation practices, ensuring adherence to approved procedures, detergents, and labeling standards
Review and verify cleaning logs, line clearance records, and housekeeping forms for accuracy, completeness, and compliance
Inspect and confirm proper use of “Cleaned” and “To Be Cleaned” tags on equipment and areas
Monitor line clearance activities to ensure removal of all previous materials, documents, and components prior to new batch startup
Document findings and escalate any nonconformance, residue, or deviation to QA management immediately
Support QA Inspectors and Production teams by maintaining a clean, organized, and inspection-ready work environment
Ensure all documentation meets ALCOA+ principles and is completed contemporaneously and accurately
Participate in internal audits, housekeeping walkthroughs, and process improvement initiatives related to cleaning verification
Perform other QA-related duties as assigned to support overall site compliance
Qualification
Required
0–2 years of experience in a cGMP pharmaceutical, manufacturing, or other regulated production environment
High school diploma or equivalent required
Basic understanding of cGMP cleaning, sanitation, and line clearance requirements
Strong attention to visual detail and cleanliness verification
Ability to complete and review documentation accurately and legibly
Effective communication and observation skills for on-floor monitoring
Strong sense of accountability, reliability, and integrity
Proficiency with Microsoft Word, Excel, and Outlook for QA documentation
Flexibility to work varied shifts, weekends, or overtime as production demands require
Preferred
Prior exposure to cleaning, sanitation, or QA monitoring activities in oral solid dosage manufacturing
Associate degree in Life Sciences or related technical discipline preferred
Benefits
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
Paid Time Off
10 paid company holidays
Comprehensive medical, dental, vision, and life insurance coverage
Professional development reimbursement
Career growth opportunities
Tuition reimbursement for children and childcare expense reimbursement
Company
KVK Tech, Inc.
KVK is a leader in the development and manufacture of high-quality, FDA-approved medicines that address unmet patient needs.
501-1000 employees
H1B Sponsorship
KVK Tech, Inc. has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (8)
2024 (18)
2023 (15)
2022 (27)
2021 (27)
2020 (28)
Funding
Current Stage
Late StageLeadership Team
A
Anthony Tabasso
President and CEO
Recent News
2026-01-01
Company data provided by crunchbase