Following up the production plan and assurance of quality according to cGMP, GDP, SOP’s & BPR.
availability of production requirements (BPR, Materials, Headcount &
machines) to achieve the required plan.
Review of all
documents during all processes to assure applying of Good documentation
update (SOP’s, BPR & Job description, etc…) to meet GDP Requirements.
Train of Shift
Leader on all section documents to achieve cGMP and GDP requirements.
employees on understanding all documents to enhance their performance.
share in any trials done in his section on new (products, materials, Ideas),
troubleshooting and Validation to enhance processes.
with Company & Corporate defined rules, SOP’s, systems, policies,
guidelines, decisions, Performance Management Systems & communicated
with HSE regulations, standards, & instructions, ensure working in a safe
manner that does not endanger self or co-workers, Observe & report unsafe
conditions, and be familiar with defined emergency plans
with HR declared policies, regulations, & targets.
mandatory training assigned on time, & Participate in personnel development
and training sessions as required.
with Company & Corporate related Quality SOP’s, GMP, ISO & MOH Standards.
other related tasks as asked by management and as arising from the business.
ensure all related procedures are updated & aligned with company &
government regulations, ensuring that all documents, forms & SOPs are
updated, communicated & strictly implemented to guarantee continuous
improvement of Function activities and compliance with defined standards.
Bachelor Degree in Pharmacy.
0-3 years of experience in related functions,
Preferred Pharmaceutical industry
Alexandria residence is a must
Years of Experience:
22 February 2021
Application End Date:
17 March 2021