QA Monitor – 2nd Shift

Responsibilities

• 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.

Requirements

• A High School Diploma or equivalent required; an 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.

Qualifications

None specified.

Skills

None specified.

Benefits

• 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

Pay

N/A

Schedule

N/A