Night-Shift QA Inspector – Parenteral Packaging

RXinsider LTD.; Cherry Hill Township (NJ); On-site; USD 27,000 - 39,000; Full time

Benefits offered by this job

Annual bonus

401(k) with company match

20 days PTO

Health benefits

Tuition reimbursement

Parental leave

Job summary

Hikma Pharmaceuticals USA Inc. is seeking a QA Inspector in Cherry Hill, NJ to monitor in-process quality for filling, inspection, and packaging of parenteral products. The role requires attention to detail and compliance with cGMPs.

The candidate should have an associate’s degree in science (or a bachelor’s) with 0–2 years in pharmaceutical QA, and be prepared for rotating shifts and occasional overtime. Onsite work with comprehensive benefits is offered.

Qualifications

• Degree in science or related field with 0–2 years in pharma or QA environment.
• Familiar with cGMPs, EU CFR and USP requirements.
• Strong attention to detail and accuracy, plus good organization.
• Able to work in a multi-tasking, team-based setting with effective communication.

Responsibilities

• Monitor in-process product quality for filling, inspection and packaging of parenteral products.
• Maintain regular onsite attendance and punctuality.
• Review test results, sample and release components and raw materials.
• Document sampling, inspection and test results clearly according to SOPs.
• Follow line assignments and assist QA Supervisor as needed.
• Support weekend rotations and overtime to back production.

Skills

Attention to detail

Team player

Good communication

Analytical skills

CFR/cGMP knowledge

Education

Associate’s degree in science

Bachelor’s degree in science

Tools

Analytical balances

Glove boxes

Pallet jack

Job description

Hikma Pharmaceuticals USA Inc. is seeking a QA Inspector in Cherry Hill, NJ to monitor in-process quality for filling, inspection, and packaging of parenteral products. The role requires attention to detail and compliance with cGMPs.

The candidate should have an associate’s degree in science (or a bachelor’s) with 0–2 years in pharmaceutical QA, and be prepared for rotating shifts and occasional overtime. Onsite work with comprehensive benefits is offered.