Senior Quality Assurance Analyst

4 semanas atrás


Sintra, Lisboa, Portugal Hikma Pharmaceuticals Tempo inteiro

Founded by Samih Darwazah over 40 years ago, Hikma Pharmaceuticals is a company with a solid foundation, committed to providing affordable, quality medicines to those who need them.

The company has a strong presence in the Middle East and has expanded its reach beyond the region, with a factory in Portugal for the production of injectable medicines. At Hikma, we are committed to recruiting the best talent to join our team and contribute to our mission of providing quality healthcare solutions.

As a Senior Quality Assurance Analyst, you will play a crucial role in ensuring the quality of our products, from raw materials to finished goods. Your responsibilities will include:

  1. Conducting or verifying analysis of bulk samples
  2. Verifying or conducting sampling and analysis of in-process control during filling of batches
  3. Conducting or verifying analysis after cleaning of machine production parts to verify clean conformity
  4. Verifying or entering data of in-process forms/logbook/LIMS on a daily basis and checking for accuracy upon request
  5. Ensuring that equipment and solutions in use are maintained under validity
  6. Sampling finished products to be tested by the Microbiology and Quality Control Departments
  7. Performing round checks in production departments, bulk packaging, and infrastructures
  8. Performing inspections in production areas whenever necessary
  9. Carrying out start-up before the beginning or during production (whenever necessary)
  10. Performing Aseptic Practices and Cleaning/Disinfection Monitoring
  11. Sampling and carrying out acceptance procedures in all phases of production, undertaking visual inspection by attributes for defects
  12. Approving maintenance requisitions for the release of production
  13. Training new QA analysts
  14. Verifying print-outs from equipment related to production activities

To be successful in this role, you will need:

  1. A High School Diploma or an Academic degree in Science
  2. The ability to handle a multi-task operation, meet tight deadlines, and work under pressure
  3. Assertiveness, flexibility, and attentiveness to detail
  4. Fluency in English and good computer skills
  5. Knowledge of the Injectables pharmaceutical industry, current Good Manufacturing Practices (cGMPs), Food and Drug Administration (FDA), and other regulatory authority requirements

In return, we offer:

  1. A salary appropriate to the functions performed
  2. High career prospects

If you think this is a role that aligns with your career goals, we invite you to join our team and contribute to our mission of providing quality healthcare solutions.



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