Analyst Quality Assurance

Job description

Founded 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 1000 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. Main Responsibilities: Perform the analysis of the in-process control testing’s; Sample the vials to be tested by the Sterility assurance and Quality Control Departments during production of each batch; Sample and prepares finished product samples for stability testing, whenever requested; Perform routine round checks in all departments; Approval all the canisters and sterbags of raw material that are delivered to production; Perform inspections in the production areas whenever necessary; Carries out the start-up before the beginning or during production; Conduct the personnel behavior to sterile core program; Sample and carries out acceptance procedures in all the different phases of the production and packaging process, and undertakes visual inspection by attributes; Sample, handle, archive, record and follow up on finished product reserve samples; Reject raw material and components delivered by production or packaging departments; Approve maintenance requisitions on the X3 for the release of production; Follows the shipping of all the products manufactured and/or packed in Hikma 2 Plant; Perform acceptance of the Returns from the Market; Define the proper corrective measures of each event related with weight deviations. Profile: High School Diploma or an Academic degree in Science Ability to handle a multi-task operation, to meet tight deadlines and to work under pressure Should be assertive, flexible, and attentive to detail Fluency in English and good computer skills are preferred Knowledge regarding 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 with rotating days off We offer: Temporary employment contract Salary appropriate to the functions performed High career prospects 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