Zeta Career - Feed https://career.zetapharma.net Zeta Career Wed, 15 Apr 2026 03:29:54 +0000 hourly 1 https://wordpress.org/?v=6.9.4 <![CDATA[Research and Development Supervisor]]> Wed, 02 Oct 2024 10:53:16 +0000 Fri, 17 Nov 2034 18:12:09 +0000 Tue, 17 Dec 2024 00:00:00 +0000 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.
  • 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.
  • Prepare Master Formula, Manufacturing, & Packaging Procedure for technology transfer of new product.
  • Ensure GMP – GDP – EHS implementation

    Job Requirements :
  • B.Sc. in Pharmacy is essential. Post graduate vis-à-vis qualifications is desired (e.g., cGMP, MBA, etc.)
  • Previous experience of pharmaceutical manufacturing and R&D is mandated backed with people management responsibility
  • Exposure and hands-on different roles at different manufacturing disciplines (e.g., Production, Quality, EHS) is a definite plus
  • Excellent verbal, written and interpersonal communication skills.
  • English fluency is essential
  • Professional computer and MS-Office skills
  • Professional analytical skills
  • Strong organizational and multitasking skills
  • Attention to detail
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