R&D Supervisor

Full time posted 11 months ago in Research and Development
  • Monufia, 7194, 7th Industrial Zone, Sadat City, 32897 View on Map
  • Post Date : October 24, 2023
  • Apply Before : April 4, 2024
  • 29 Application(s)
  • View(s) 905
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Job Detail

  • Job ID 3893
  • Career Level Experienced Non-Manager
  • Experience (Min Years) 3
  • Experience (Max Years) 5
  • Age not less 26
  • Age not exceed 28
  • Education Level Bachelor\'s DegreeDiploma or equivalent
  • Gender All Gender
  • Industry Pharmaceutical
  • Nationality Egyptian

Job Description

  • 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.
  • 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 Pilot 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.
  • Provide technical/scientific leadership within department and serves as a department representative on cross-functional teams and professional affiliations.
  • 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.
  • Ensure GMP – GDP – EHS implementations.
  • Prepare the documents for new products registration requirements.
  • Follow up / supervise the safe and healthy work environment.

Required skills

Ambiguity Analytical Communication Details Oriented Innovation Leadership R&D Resilience

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