Quality Assurance Inspector

Quality Assurance Line Inspector – 2nd Shift

Location: Bethlehem, PA

Shift: 2nd Shift (3:00 PM – 11:30 PM)

Duration: 3-month contract (possible extension or direct hire)

Pay Rate: $20–$23/hour

Job Overview:

We are seeking an experienced Quality Assurance (QA) Line Inspector to support packaging operations at a pharmaceutical manufacturing site. This is an urgent, immediate need for a 3-month contract position with potential extension or direct hire based on business need and performance.

Responsibilities

• Provide QA presence on the packaging line to ensure overall product quality.
• Perform line clearance and start-up inspections; authorize start of packaging runs.
• Document all packaging line activities in accordance with established procedures.
• Issue master batch records and generate Bills of Materials (BOMs) for packaging.
• Verify that all materials/components used in packaging runs match the approved BOM.
• Maintain, review, complete, and control packaging batch records to ensure accuracy and compliance.
• Document in-process inspections and retain required samples.
• Control and label finished goods leaving the packaging area (Released, Quarantined, etc.).
• Ensure proper usage, disposition, and destruction of unused packaging components (cartons, labels, inserts, etc.).
• Communicate any issues affecting packaging line clearance, setup, and inspections.
• Provide oversight and support to packaging teams regarding quality concerns.
• Report manufacturing/packaging issues, safety concerns, and personnel concerns to appropriate leadership.
• Support procedure updates and revisions related to packaging QA activities.
• Assist with special projects and additional assignments as needed.
• Willingness to work overtime and provide coverage as needed, including possible weekend work.

Qualifications

• Associate degree (2-year degree) in a science or technical field preferred.
• 3 years of relevant QA experience in a pharmaceutical, biotech, or regulated manufacturing environment MANDATORY.
• Strong understanding of pharmaceutical cGMP requirements, industry standards, and regulations.
• Excellent verbal and written communication skills.
• Strong attention to detail and organizational skills, especially related to batch record documentation.
• Ability to work effectively across departments and with different levels of leadership.
• Proficiency with Microsoft Office (Outlook, Excel, Word).
• Experience with systems such as SAP and TrackWise is a plus.
• Strong critical thinking and problem-solving skills.

Physical Requirements

This role requires the ability to stand and walk for extended periods, perform repetitive hand motions, and occasionally lift or carry up to 50 lbs.