Following up the production plan and assurance of quality according to cGMP, GDP, SOP’s & BPR.
Check the availability of production
requirements (BPR, Materials, Headcount & machines) to achieve the required
Review of all documents during all processes to
assure applying of Good documentation practices.
Issue and 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.
Evaluate all employees on understanding all
documents to enhance their performance.
Attend and share in any trials done in his
section on new (products, materials, Ideas), troubleshooting and Validation to
1- Comply with Company & Corporate
defined rules, SOP’s, systems, policies, guidelines, decisions, Performance
Management Systems & communicated targets.
2- Comply 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
3- Comply with HR declared policies, regulations, & targets.
Complete mandatory training assigned on time, & Participate in personnel
development and training sessions as required.
4- Comply with Company & Corporate related Quality SOP’s, GMP, ISO &
5- Fulfill other related tasks as asked by management and as arising from the
6- Commit, 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.
B.Sc. in Pharmaceutical Science.
Years of Experience:
23 March 2021
Application End Date:
8 April 2021