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.