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RD Formulation Supervisor At Zeta Pharma

 RD Formulation Supervisor At Zeta Pharma 

RD Formulation Supervisor At Zeta Pharma






Location :  El Sadat City, Al Minufiyah, Egypt

Zeta Pharma is hiring R&D Formulation Supervisor

Location: Sadat City

JOB SUMMARY

Execute formulation activities including and not limited to new products preformulation and formulation, pilot scale manufacturing, materials availability, quality, safety issues

-Bachelor degree of pharmacy

-At least 3-4 years’ experience as R&D Formulation

 

Conduct periodic meetings with subordinates for reviewing progress and work flow, discussing their suggestions and taking suitable actions accordingly.

Follow-up subordinates’ affairs including vacations, leaves …etc.

Conduct performance appraisals for subordinates according to scheduled plans and recommend necessary actions as per the applied practices at the company.

Prepare periodic reports with respect to the activities and achievements to be submitted to the direct supervisor for review

Perform Literature survey on drug substance and drug product of the originator.

Check the patency status

Suggest the suitable Formula and manufacturing process technique.

Suggest the new API and Excipients suitable specification Range

Check the materials quantity, retest date & expiry date in the laboratory storage area.

Issue material requisition for any material shortage.

Coordinate with supply chain dep. for scheduling the requested materials.

Check the received materials certificate of analysis, storage condition and MSDS for proper handling and storage.

Prepare batch record for lab scale manufacturing and packaging procedure.

Supervise, motivate and guide the correct operation of the manufacturing and packaging procedure for Lab scale, pilot scale and validation batches.

Supervise, motivate and guide the correct assembling and disassembling of machines and apparatus.

Supervise, motivate and guide the correct cleaning procedure for machines and apparatus.

Review analysis results and figure out the potential factors for optimization.

Update the formulation sops in upgraded technical and quality aspects.

Perform technical training and follow up implementation.

Prepare Master Formula, Manufacturing, & Packaging Procedure for technology transfer of new product.

Prepare Product development protocol and report and other relevant documents

Prepare the documents for new products registration requirements.

Ensure GMP – GDP – EHS implementations.

Minimize the product development cost of materials, tools and machines.

Review MSDS for each API and record the safety precautions and first aid measures in the batch record.

Follow up / supervise the safe and healthy work environment.

In cooperation with EHS department, Establish EHS Risk management for formulation lab and implement the control measures.

Supervise the pharmaceutical and packaging Waste disposal.

Follow up machines’ preventive maintenance and calibration end date.

 

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