Quality Assurance Inspector

Summary

We continue to be committed to building a diverse and inclusive team and encourage applications from candidates of all backgrounds. We are seeking a talented and motivated QA Inspector, QA. In this role, you will be responsible for monitoring in-process product quality for Filling and Inspection and Packaging of parenteral products. The QA Inspector is responsible for performing visual and functional testing of product against statistically based sampling plans. In addition, the QA Inspector performs routine inspection and testing of components in accordance with Standard Procedures and specifications as required by production scheduling. In performing the above duties, the individual is responsible for accurately and clearly documenting test results in accordance with cGMPs. This position participates in rotation for weekend coverage and as needed during the work week.

Job description

Requirements

• 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).
• Possesses proficient mathematical skills (addition, subtraction, multiplication, division, algebra, unit conversions, rounding significant figures, dividing polynomials, solving rational equations).
• Familiar with cGMPs, EU, CFR and the USP
• Demonstrates good attention to detail and accuracy
• Good organizational skills and ability to multi-task and perform work in a timely manner
• Demonstrates ability to work in a team environment with good communication skills and ability to communicate effectively with peers, department management and production personnel
• Knowledge of computer systems at a level proficient to navigate input and/or reference computerized data
• Must have sound judgment and demonstrate good analytical skills to assess risk to issues related to the manufacturing process
• Must be able to pass the respirator requirements established for the Inspector position
• Ability to stand/walk 85% of the shift to sample raw material and deliver to labs
• Good manual dexterity to repetitively manipulate syringes to sample filled units for in-process monitoring
• Good close visual acuity (eye exam required)
• Noise levels on production lines may be moderate to high
• Able to lift 15 lbs.
• Able to pull/push raw materials with use of a pallet jack.
• Prior QA experience preferred.

Company overview

Hikma Pharmaceuticals PLC is a multinational pharmaceutical company headquartered in London, United Kingdom, with a significant presence in the Middle East and North Africa (MENA) region and the United States. Founded in Jordan in 1978, Hikma has grown into one of the world's leading generic pharmaceutical companies, specializing in the development, manufacturing, and marketing of branded and non-branded generic medicines. The company operates through three main business segments: Generics, Injectables, and Branded products. Hikma's portfolio includes a wide range of therapeutic areas such as oncology, cardiovascular, central nervous system, and anti-infective medications. With manufacturing facilities across multiple countries and a strong focus on quality and regulatory compliance, Hikma serves healthcare providers and patients in over 50 countries worldwide. The company is publicly listed on the London Stock Exchange and is a constituent of the FTSE 250 Index, demonstrating its significant market presence and financial stability in the global pharmaceutical industry.