Quality Assurance Supervisor

؜ - ؜6th of october city ؜ -

تفاصيل الوظيفة


  • Perform Internal and external audits in addition to audit program planning. Prepares the audit and observation reports. Follows up audit action plans.

  • Batch records revision and release of AstraZeneca Egypt products to Egyptian market as deputy for Quality Lead.

  • Prepares, updates the QA SOPs, and review other functions GMP SOPs, instructions, records and logbooks.

  • Participate in setting the site's GMP training plan according to business priorities. Provides GMP training to site employees.

  • Follows up and support the embedding of quality culture by ensuring the right behaviours are followed at all stages of operations, awareness, and proper documentation.

  • Address trends of GMP observations and incidents. Contribute in issuing the site's improvement plans.

  • Contribute in problem solving & investigation after any incidence.

  • Follow up CAPA implementation.

  • Participate and ensure the validation of all products and processes. Follow up of validation and qualification activities till completion and issuing final reports

  • Responsible for the safe archive and maintenance of validation and qualification documents in accessible protected cabinets.

  • Participate in preparing Annual Product Review reports.

  • Contribute in the Quality Management Review meeting.

  • Participate in Lean Project as per the site's Lean plan.

  • Support new QA officers by training for GMP and SHE

  • Present the QA in the site daily Tier ‎3 and monitors the effectiveness of the QA daily GENBA tours in Production.

  • Following SHE policies, Adhere and follows Code of Ethics

  • Ensure own work is compliant with health, safety and cGMP

  • Perform all the required activities in accordance with the local regulatory requirements.

  • Receive and Respond to the updates of the regulatory decrees and laws according to the local instructions.

  • Ensure that imported bulks, API's and finished goods packed from imported bulks are released to the local market according to the requirements of the health authorities.

  • Perform all required risk assessment studies in accordance with the local procedures.

  • Contribute in the identified site quality risks

  • Special tasks for the person

  • Contribute in preparation of the Plant Master File to be reviewed and approved by the Quality Lead

  • Experience: ‎5 - ‎7 years in Quality function

ملخص الوظيفة

  • المُعلن : AstraZeneca
  • تاريخ الإعلان : 21/12/2022
  • نوع العمل : -
  • مستوى الخبرة : -
  • المستوى التعليمي : -
  • مكان العمل : 6th of october city
  • الراتب : -
  • الهاتف : -

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