Title: Analyst, Quality AssuranceFounded by Samih Darwazah over 40 years ago in Jordan, Hikma's purpose is to provide affordable, quality medicines to the people who are competent. 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 extended ours 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 an Analyst, Quality Assurance (m/f) to integrate Quality Assurance Department, on-site work, in a rotating shift system from Monday to Friday, and later from Tuesday to Saturday with a fixed night shift.
Main Responsibilities: Conducting or verifying analysis of bulk sampleVerifying or conducting sampling and analysis of the in-process control during filling of the batchesConducting or verifying analysis after cleaning of machine production parts to verify clean conformityVerify or enter the data of the in-process forms/logbook/LIMS on a daily basis and check for accuracy upon requestEnsures that the equipment's and solutions in use are maintained under validitySample finished product to be tested by the Microbiology and Quality Control DepartmentsPerforms round checks in production departments, bulk packaging and infrastructuresPerforms inspections in the production areas whenever necessaryCarries out the start-up before the beginning or during production (whenever necessary)Performs Aseptic Practices and Cleaning/Disinfection MonitoringSamples and carries out acceptance procedures in all the different phases of the production, undertakes visual inspection by attributes for defectsApproves maintenance requisitions for the release of productionTrains new QA analystVerifies print-outs from equipment related with productions activitiesProfile: High School Diploma or an Academic degree in ScienceAbility to handle a multi-task operation, to meet tight deadlines and to work under pressureShould be assertive, flexible, and attentive to detailFluency in English and good computer skills are preferredKnowledge regarding the Injectables pharmaceutical industry, current Good Manufacturing Practices (cGMPs), Food and Drug Administration (FDA) and other regulatory authority requirementsWe offer: Salary appropriate to the functions performedHigh career prospectsIf you think this is a good opportunity for your professional career, join us and contribute to Better Health, within everyone's reach, every day.
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