Pharma QA Inspector – Parenteral Fill/Inspect

Hikma Pharmaceuticals; Cherry Hill Township (NJ); On-site; USD 48,000 - 68,000; Full time

Benefits offered by this job

Annual bonus

401(k) company match

Paid time off 20 days

Health, dental, vision

Parental leave

Career growth

Job summary

Hikma Pharmaceuticals USA Inc. is seeking a QA Inspector to monitor in-process product quality for filling, inspection and packaging of parenteral products at our Cherry Hill, NJ site.

The role emphasizes attention to detail, adherence to cGMPs, and coordination with QA to ensure timely release of components and materials. The candidate will perform sampling, documentation and QA support, with shift timing from Tuesday to Saturday 3:10PM–11:20PM, and participate in weekend rotations to support

Qualifications

• Associate’s degree in science or Bachelor’s Degree with 0-2 years applicable laboratory, pharmaceutical manufacturing, or related experience.
• 0-2-year applicable laboratory or pharmaceutical production experience (QA preferred).
• Familiar with cGMPs, EU CFR and the USP.

Responsibilities

• Regular and predictable onsite attendance and punctuality.
• Performs in-coming tasks including pallet checking, raw material sampling, review of test results, release of components, raw materials and production supplies.
• Contacts QA Coordinator or QA Supervisor for daily line assignments.
• Samples/Checks/Verifies Controlled Substances during in-coming monitoring and raw material sampling.
• Must pass frocking qualification for controlled areas and pass respirator requirements for sampling raw materials.
• Maintains good housekeeping and safe working conditions.

Skills

Attention to detail

Teamwork

Communication

Problem solving

Education

Associate’s degree in science

Bachelor’s degree in science

Tools

Analytical balances

Glove boxes

Analytical instruments

Job description

Hikma Pharmaceuticals USA Inc. is seeking a QA Inspector to monitor in-process product quality for filling, inspection and packaging of parenteral products at our Cherry Hill, NJ site.

The role emphasizes attention to detail, adherence to cGMPs, and coordination with QA to ensure timely release of components and materials. The candidate will perform sampling, documentation and QA support, with shift timing from Tuesday to Saturday 3:10PM–11:20PM, and participate in weekend rotations to support