Coordinator, Quality Assurance

Description

Summary: Hikma Pharmaceuticals is seeking a Quality Assurance Analyst to conduct and verify analyses of samples, perform inspections, and monitor aseptic practices. Highlights: 1. Conduct or verify analysis of bulk samples and in-process control 2. Perform inspections and round checks in production departments 3. Train new QA analysts and verify equipment print-outs Apply now » Apply now Apply now Apply with LinkedIn Start Please wait... **a.dialogApplyBtn { display:** none; } **Date:** 23/07/2026 **Location:** Sintra, Sintra, PT **\#job\-location.job\-location\-inline { display:** inline; } **Company:** Hikma Pharmaceuticals PLC Founded by Samih Darwazah over 40 years ago in Jordan, Hikma's purpose is to provide affordable, quality medicines to the people who need them. Based on very solid foundations, we continue to innovate daily and find practical solutions to transform the lives of the millions of people we serve. At the end of the 1980s, we expanded beyond the Middle East and acquired land in Portugal for the construction of a sterile factory for injectable pharmaceutical products. This was an important turning point for the company, and our first step into a new region. Today, in Portugal, we have more than 900 employees and 3 factories for the production of injectable medicines. Hikma intends to recruit a Quality Assurance Analyst (m/f) to join the Quality Assurance Department, for on-site work. **Main Responsibilities:** Conducting or verifying analysis of bulk samples; Verifying or conducting sampling and analysis of in-process control during batch filling; Conducting or verifying analysis after cleaning machine production parts to verify cleanliness conformity; Sampling finished products for testing by the Microbiology and Quality Control Departments; Performing round checks in production departments, bulk packaging, and infrastructure; Performing inspections in production areas whenever necessary; Carrying out the \-up before the start or during production (whenever necessary); Performing Aseptic Practices and Cleaning/Disinfection Monitoring; Sampling and carrying out acceptance procedures at all different production stages, performing visual inspection by attributes for defects; Approving maintenance requisitions for production release; Training new QA analysts; Verifying print-outs from equipment related to production activities. **Profile:** Bachelor's degree in Science; Ability to handle multi-task operations, meet tight deadlines, and work under pressure; Should be assertive, flexible, and detail-oriented; Fluency in English and good computer skills are preferred; Knowledge of the injectables pharmaceutical industry, current Good Manufacturing Practices (cGMPs), Food and Drug Administration (FDA), and other regulatory authority requirements; Availability to work 8-hour shifts; Personal vehicle required. **We offer:** Direct contract with Hikma; Competitive salary aligned with the role; Life insurance; Health Insurance extended to student children (up to age 24); Annual Performance Bonus; Real Growth Opportunities. If you think this is a good opportunity for your professional career, join us and contribute to Better Health, within everyone's reach, every day Apply now » Apply now Apply now Apply with LinkedIn Start Please wait... **a.dialogApplyBtn { display:** none; }