Orchidia Pharmaceutical Vacancies
1-Quality Assurance Specialist (QA IPC)
Job Description
Inspection on the dispensing process.
Inspection on the division of the ware house the release area, guarantee area and the reject area with the true identification labels.
Follow up the check list of the RH, Temp. At the different places at the ware house.
Inspection on the destruction process for the rejected finished products, raw materials and packaging materials.
Inspection on the raw and packaging materials and ensure its comply with the acceptance criteria.
Inspection on the gowning according to the SOP.
Inspection on the preparation process including check the weight of the raw materials, changing the filters, the CIP process and the SIP process.
Inspection on the autoclave activities with different sterilization programs.
Inspection on the filling process at the filling room and ensure that the area is clean from any previous product and that the machine is cleaned and sterilized for the new product.
Check the environmental monitoring for the sterile area.
Check the RH, the temp. And the Δp of all the sterile area according to its classification.
Check the weight, the shape and the sealing of the filled bottles.
Inspection on every process according to the batch record and ensure that the line clearance process are completed between every product.
Taking the samples to the Q.C department as the bulk sample: for ph. and assay, bio burden for microbiology.
Taking the samples to the Q.C department as S.F.P. sample: for finished analysis and sterility analysis.
Review the recording of all the production steps at the batch process and the batch packaging.
Release the batch to the guarantee area after the final reconciliation by the yellow label, then by the green label after the certificate of the chemical and microbiological analysis.
Include recording all the deviation which occurs at all the production process and writing the corrective and preventive action.
Recording any complain from any customer from any product and investigate about the reason of the problem and solving it.
Making internal audit on all the departments of the factory and recording the points which deviate from the right process and informing each department by its point to follow up this points and solving it then inform the QA by the corrective action which they did.
Skills
– Bsc. Degree in Pharmaceutical Science.
– One year experience in pharmaceutical operations.
– Understanding of methodologies and best QA practices
– Knowledge of documentation reviews and requirements analysis.
– Ability to troubleshooting and resolving complex issues effectively.
– Excellent English, verbal / written communication
– Ability to work well through others
– Excellent computer skills
Education
Pharmacy
Job Details
Job Location
Cairo, Egypt
Job Role
Quality Control
Employment Status
Full time
Employment Type
Employee
Manages Others
No
Number of Vacancies
2
Preferred Candidate
Career Level
Entry Level
Years of Experience
Min: 1 Max: 3
Residence Location
Cairo, Egypt
Gender
Male
Degree
Bachelor’s degree
Interested Candidates send their CVs to ahmed.elnady@orchidiapharmaceutical.com Mentioning position name in subject
2-R&D Stability Pharmacist
Job Description
Participate in Translating business goals into plans that cover local market and export.
Participate in Preparation of new products stability files to be registered and launched onto the market in accordance with local regulatory requirements and requirements of export under the general supervision of the R&D manager.
Execute plan of stability studies covering first three batches, process validation, and change or add supplier, change composition & ongoing stability study covering for all products.
Monitor of stability temp. & humidity and ensure of archiving them
Prepare protocol for each stability studies containing summarized data and results.
send stability samples for micro analysis (sterility or preservative effectiveness test) for long , Acc. & in use
analysis of the new product under stability condition must meet the product specification especially impurities
update SOPs related to stability system & covering R&D activities
Report problems relating to products in stability chambers to R&D manager immediately.
Maintain & enhance capacity of stability chambers to cover different dosage form
Work according to R&D safety system.
Work according of GLP requirements
Skills
Bachelor’s degree a must, in Pharmaceutical science.
One year of technical experience in stability, analytical method validation and training preferably in the pharmaceutical industry.
Scientific, technical background in pharmaceutical as well as cosmetics products is beneficial.
Using an advanced knowledge of stability and method validation techniques.
Excellent English, verbal / written communication.
Ability to communicate well and work through others.
Excellent computer skills.
Self-Motivating.
Creative.
Good problem solving skills.
Good communications skills.
Good self-management skills.
Capable of working in a team environment.
Education
Pharmacy
Job Details
Job Location
Cairo, Egypt
Job Role
Research and Development
Employment Status
Full time
Employment Type
Employee
Manages Others
No
Number of Vacancies
2
Preferred Candidate
Career Level
Entry Level
Years of Experience
Min: 1 Max: 3
Residence Location
Egypt
Nationality
Egypt
Degree
Bachelor’s Degree