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QA EXPERT
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                                                  MEET THE EXPERTS!!!

 KLEVA Pharmaceuticals S.A. is a privately owned pharmaceutical company that has been in operation in Greece since 1974. Kleva develops and manufactures generic products and focus on Pharmaceuticals (Rx & OTC).

KLEVA has a fully integrated company with R&D, RA, Production, QC, QA, Marketing and Sales departments.

Our factory in Athens, Greece, is equipped with the latest technology machinery and has the manufacturing potential for a wide range of pharmaceutical forms.

Our mission is to offer a flexible, fully scalable, qualitative, and cost-effective product development in a wide range of dosage forms. We register and export our products to a number of regulated and non-regulated markets around the world.

To realize our ambitious goals, KLEVA needs people who are innovators, believe in the values of respect and cooperation and are ready to commit to a company that wants to penetrate new markets, leverage international business development opportunities, and enter contract manufacturing deals.

How you will support our mission

We are looking for a Quality Assurance Expert.

Requirements:

  • drafting quality assurance policies and procedures
  • interpretation and implementation of quality assurance standards
  • review the implementation and efficiency of quality and inspection systems
  • performing of internal/external audits-drafting of audit reports
  • investigation customer complaints and non-conformance issues
  • collection, compilation and assessment of statistical quality data
  • Recommendation and monitoring of the corrective and preventive actions
  • preparation reports to communicate outcomes of quality activities
  • Drafting and execution of risk management activities and reports
  • Responsible for the implementation of the Cleaning Validation program
  • Assurance of ongoing compliance with quality and industry regulatory requirements
  • Preparation of PQRs, Process and Cleaning Validation Protocols/Reports
  • Assistance and coordination for Change Control documents

 

 Qualifications:

  • Professional experience of at least 2 years in the QA dept of a pharmaceutical industry.
  • Bachelor degree in Chemistry, Biology, Chemical Engineering or other related field.
  • Fluency in English both written and oral Strong computer skills including Microsoft Office, QA applications and databases.
  • Knowledge of tools, concepts and methodologies of QA.
  • Knowledge of relevant regulatory requirements.

 

With DEI in mind!!!

Diversity, equity, and inclusion are a priority for us! KLEVA ensures a safe and balanced working environment, based on respect by providing an equal number of opportunities to every employee who meets the necessary requirements.

Here @KLEVA, we care for your privacy. The security of your data is one of our greatest concerns. All information is strictly confidential and in accordance with GDPR rules.

 

                                Meet our hiring team…and apply now!!!!

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QA EXPERT
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