Validation Specialist At Rameda Pharmaceuticals
Rameda is Egypt's fastest-growing leading pharmaceutical company, 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 allowed 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:
"QA Validation Specialist "
Description
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1-Participating in GMP Projects, different validation working parties.
2-Checking and follow up the site validation review plans for (building, HVAC system, services and equipment).
3-Ensuring (under direct supervision of validation section head) that all validation activities and documentation are complying with the recommendations of guidelines as well as VMPs and product master file.
4-Share in preparing the Validation Master Plans (VMP) , design qualification ,installation Qualification & operation Qualification and Performance Qualification Protocols (PQPs) and Validation reports (VR) for different validation activities such as:
A)- Process validation.
B)- Cleaning validation.
C)- Thermal Mapping.
D)- Media fill.
E)- Internal & External Calibration.
F)- Internal & External Qualification.
G)- Annual product quality review (APQR).
H)- Holding Time for Pharmaceuticals during Manufacturing Process.
5- Following up the following activities to review and approve them:
· Receiving all calibration certificates, follow its approval and filing.
· Filing all validation deliverables and retrieving them professionally.
· Review for all new standard operating procedure related the validation section.
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Qualifications
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1-Bachelor’s degree in Pharmacy or Science
2-Minimum of 1 year experience in the same position
3-Excellent written and verbal communication skills.
4-Incumbent must be a dynamic and hard-working professional with a background in Quality Assurance and must be detail-oriented and self-motivated.
5-Strong analytical skills and attention to detail.
6-Good background of Pharmaceutical manufacturing&ISO requirements.
7-Good background of GLP, GMP, GEP.
8-Good experience of Qualification and Calibration
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We offer:-
1- One of the top highest market packages
2- Continuous training and development programs
3- Promising career pathways
4- Tempting incentive scheme
* Candidates that matches above qualifications, send your resume to career@rameda.com,mentioning the job title in the subject
"QA Validation Specialist "
Description
--------------
1-Participating in GMP Projects, different validation working parties.
2-Checking and follow up the site validation review plans for (building, HVAC system, services and equipment).
3-Ensuring (under direct supervision of validation section head) that all validation activities and documentation are complying with the recommendations of guidelines as well as VMPs and product master file.
4-Share in preparing the Validation Master Plans (VMP) , design qualification ,installation Qualification & operation Qualification and Performance Qualification Protocols (PQPs) and Validation reports (VR) for different validation activities such as:
A)- Process validation.
B)- Cleaning validation.
C)- Thermal Mapping.
D)- Media fill.
E)- Internal & External Calibration.
F)- Internal & External Qualification.
G)- Annual product quality review (APQR).
H)- Holding Time for Pharmaceuticals during Manufacturing Process.
5- Following up the following activities to review and approve them:
· Receiving all calibration certificates, follow its approval and filing.
· Filing all validation deliverables and retrieving them professionally.
· Review for all new standard operating procedure related the validation section.
---------------------------------------------------------------------------------
Qualifications
---------------
1-Bachelor’s degree in Pharmacy or Science
2-Minimum of 1 year experience in the same position
3-Excellent written and verbal communication skills.
4-Incumbent must be a dynamic and hard-working professional with a background in Quality Assurance and must be detail-oriented and self-motivated.
5-Strong analytical skills and attention to detail.
6-Good background of Pharmaceutical manufacturing&ISO requirements.
7-Good background of GLP, GMP, GEP.
8-Good experience of Qualification and Calibration
-----------------------------------------------------------------
We offer:-
1- One of the top highest market packages
2- Continuous training and development programs
3- Promising career pathways
4- Tempting incentive scheme
* Candidates that matches above qualifications, send your resume to career@rameda.com,mentioning the job title in the subject