, pub-2091334367487754, DIRECT, f08c47fec0942fa0 Lot Release Specialist At Rameda Pharmaceutical Company

Lot Release Specialist At Rameda Pharmaceutical Company

 Lot Release Specialist At Rameda Pharmaceutical Company

Lot Release Specialist At Rameda Pharmaceutical Company

Rameda is the fastest-growing leading pharmaceutical company in Egypt, led by a team of professionals with extensive multinational experience. The Company develops and produces a wide range of branded generic pharmaceutical products.Rameda combines global standards with local insights, you are given the opportunity to gain experience professionally through an environment that supports and provides you with the tools you need to learn and move forward in your career. We are committed to attract and retain exceptionally talented employees; therefore, we are looking to hire the following post: -

"Lot Release Specialist"

-  Keeping registration papers for all products and any update requirements.
-  Entering database for all rameda products.
-  Preparing, and reviewing all papers related to raw materials received by the company.
-  Reviewing, and approving received packaging materials against EDA-approved ones.
-  Reviewing, and approving for lot release of finished products after being sure that all documents needed for release are submitted.
-   Follow up on the status of all products sent to NODCAR (inspection department) till approval.
-   Preparing and Keeping all documents related to the EDA inspector visit as (sampling reports for products,sampling reports of raw materials,release reports for finished products and for raw materials also any documented observations she done during her visit any conformities received by her any NODCAR letter received by her or nonconformity reports)
-   Follow up with QC to full fill NODCAR comments on time.
-   Responsible for doing MRB(material review board), determining committee members, and following up until the last decision.
1-BSC in pharmacy or science
2-Experience in Deviation Management and batch disposition.
3- Auditing and technical report writing experience.
4-Expert knowledge and understanding of GMPs, keeping up to      date with current industry issues and changing regulations.
5-High accuracy level to guarantee the reliability of results.
6-Individual must be a dynamic and hard-working professional with a background in Quality Assurance

We offer:

·        Competitive package
·        Attractive incentive scheme
·        Continuous training and development
·        Promising Career Pathways

* Candidates that matches the above qualification kindly send your resume to: with mentioning the job title in the subjec