Research and Development Supervisor At Zeta Pharma
Zeta Pharma is a well-established and fast-growing pharmaceutical company dedicated to improving the lives of patients through innovative healthcare solutions.
We are currently seeking for a highly organized, analytical Research and Development Supervisor to join the R&D Zeta Plant team.
Job Responsibilities:
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.
Prepare Master Formula, Manufacturing, & Packaging Procedure for technology transfer of new product.
Ensure GMP – GDP – EHS implementations.
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 details
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