QC Analyst

Jamjoom Pharma has in a very short span of time emerged, as one of the leading pharmaceutical companies in the Afrasia region. The geographical focus of the company is on countries in the Middle East, Africa, and CIS regions. Strategic focus on selected therapeutic categories has contributed to the rapid growth, market acceptance, and overall success of the company.

*Candidates With Special Needs are Welcome to apply , please indicate at the top of your CV.

Main job responsibilities:

• Development of Raw materials/ Finished product SOPs
• Development of Packaging materials SOPs
• Reviewing Sampling plans with sampler prior to sampling of raw/ Finished product  and packaging materials
• Coordination between sampler and warehouse staff concerning sampling process .
• Coordination with QA Staff concerning artwork and approved packaging forms .
• Supervision of Laboratory technician while analyzing water samples
• Supervision of Day-to-Day activities related to analysis of raw/ Finished product and packaging materials
• Reviewing analysis results of raw/ Finished product and packaging materials prior to issuing COA
• Reviewing release / reject labels printing prior to their attachment on materials .
• Reviewing Volumetric standards preparation and standardization prior to introduction of volumetric solution to lab
• Reviewing Working standards preparation prior to introduction of working standards to lab
• Monthly check and review of reference standards stock state and issuing purchase request of needed standards .
• Monthly check and review of working standards stock state and initiating cycle of preparation of needed standards .
• Ensuring correct implementation of existing procedure related to Data integrity and audit trails.
• Creation of worksheets related to raw / Finished product and packaging materials.
• Management of chemical store
• Management of glass store
• Ensuring correct implementation of existing procedures related to retained samples. 
• Ensuring that laboratory technician correctly calibrated instruments to be calibrated on daily basis .
• Creation of Validation protocols for raw materials / Finished product  analytical test methods in case required by EDA.
• Reviewing raw materials / Finished product analytical test methods .
• Double checking the OOS Checklist for obvious lab errors whenever Raw / Finished product  and Packaging materials analysis were found to be non-conforming.

Qualifications:

• Bachelor's degree in pharmaceutical science or Science.
• 3-5 years of experience in RM / PM in the pharmaceutical industry.
• Good analytical and instrumentation background.
• Good knowledge of DI, GDocP, cGMP, GLP safety regulation and EDA regulatory guidelines.
• Good technical experience in analytical testing with its related aspects.
• Good technical experience with global Pharmacopeias (Ex. USP, BP, EP, … etc.).
• Good English language and good computer skills.