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Pharmacist

Posted 24th Jan, 2025
Expires on 31st Mar, 2025

About the role

Job Description

Roles & Responsibilities

Responsibilities


1. Documentation:




a. Complete and endorse all necessary manufacturing, packaging and quality control documentation.




b. Maintain a register of all released batches in accordance with approved procedures, GMP, ISO 9001:2015, ISO 13485:2016, ISO 15378:2017 and regulatory requirements.




c. Approve specifications of raw materials, packaging materials, bulk products, and finished products.




d. Ensure that all procedures and documents related to batch records revision are up to date.




e. Ensure all requirements under references have been met prior to release of a batch in compliance with MOH.




2. Quality Control activities:




a. Review and approve the stability report of the products and designate appropriate storage condition and expiry dates based on stability result.




b. Review Physico-chemical and microbiological batch records.




c. Ensure that all necessary quality control checks and tests have been performed, and account taken of the manufacturing and packaging conditions including a review of batch records.




d. Ensure that all necessary checks and tests have been performed including any additional sampling; inspection; tests or checks initiated because of deviations or planned changes.




e. Ensure that the starting materials, packaging materials, intermediate, bulk and finished products are in compliance with the requirements.




f. Conduct product annual review.




g. Ensure that the principal manufacturing and testing processes have been validated.




h. Promote GMP through training and guidance internally.




I. Follow and apply plant hygiene procedures in a very strict way.




j. Implement all operations in accordance with written procedures and all testing operations according to the approved methods once needed.



3. Inspection and monitoring:




a. Inspect production batch records and ensure all requirements related to the quality of products during the manufacturing process are met.




b. Monitor and ensure compliance with the requirements of GMP, ISO 9001:2015, ISO 13485:2016, ISO 15378:2017 and international pharmacopeias (USP and EP).



Qualifications




Education: Bachelor's degree in pharmacy




Languages: Arabic and English




Experience: 0-1 year




Skills:




Excellent verbal and written communication skills


Quality focus


Attention to details


Problem solving

Company Industry

  • MedicalHealthcareDiagnosticsMedical Devices



1 years

Required skills

Management Skill

Other Information

1
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