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 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.
Main Responsibilities:
Conducting or verifying analysis of bulk sample
Verifying or conducting sampling and analysis of the in-process control during filling of the batches
Conducting or verifying analysis after cleaning of machine production parts to verify clean conformity
Verify or enter the data of the in-process forms/logbook/LIMS on a daily basis and check for accuracy upon request
Ensures that the equipment's and solutions in use are maintained under validity
Sample finished product to be tested by the Microbiology and Quality Control Departments
Performs round checks in production departments, bulk packaging and infrastructures
Performs inspections in the production areas whenever necessary
Carries out the start-up before the beginning or during production (whenever necessary)
Performs Aseptic Practices and Cleaning/ Disinfection Monitoring
Samples and carries out acceptance procedures in all the different phases of the production, undertakes visual inspection by attributes for defects
Approves maintenance requisitions for the release of production
Trains new QA analyst
Verifies print-outs from equipment related with productions activities
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
We offer:
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
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