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Biological science jobs,Production supervision jobs,Industrial chemistry jobs,Analytical chemistry jobs,Biochemistry jobs,

Deadline: 2021-12-31

 Production Supervisor

Duties and Responsibilities

  • Follow weekly shift plans and daily set production schedules to execute all assigned tasks as per the work instructions.
  • Performing Autonomous Maintenance tasks on the assigned equipment. These are industrial filling machines, greenhouses, motors, chain-belts, hoppers
  • Attend scrum meetings and other sessions called by the line manager to discuss and resolve work challenges
  • Lead scrum meetings in your sections
  • Proactively propose to your supervisor possible solutions to challenges affecting productivity, quality, health & safety in your work area
  • Lead workmen at your section to resolve agreed issues
  • Actively support and be involved in maintenance activities related to equipment in your assigned factory section
  • Meet biweekly with your line manager to review and set expectations for your performance
  • Meet biweekly with your reports to review and the set expectations for their performance
  • Report your sections performance against set production schedules to your supervisor on a daily basis on the established platforms
  • Training new or existing operators on equipment operations and execution of daily tasks
  • Building healthy, prosperous communities
  • Work with other section supervisors to ensure that processes run in sync as per the production schedule
  • Lead your teammates in your section to execute daily production schedules
  • Attend and actively participate all team meetings
  • Maintain effective working relationships through treating your colleagues with respect
  • Resolve misunderstandings and report unresolved issues with suggestions to your Supervisor or talent partner
  • Have cordial interactions with the community as you do your work
  • Report any complaints or concerns raised by existing customers or any other member of the community
  • Adhere to set shift plans and work orders
  • Proactively ask or seek clarification from your Supervisor on any areas of work that are unclear
  • Openly share ideas during scrum and team meetings on how current processes can be improved
  • Participate in new improvements initiatives as assigned by your supervisor
  • Use resources assigned to you sparingly as per the resource plan shared by your Supervisor
  • Use and handle assigned company assets as per set policy
  • Conduct scheduled Gemba/factory walks in your area/section to identify opportunities for process improvement
  • Coach fellow workmen and support them to understand the process and equip them to detect and/or
  • challenges/variances in the line of their day to day duties

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  • Experience in leading line staff/factory staff (2 years)
  • At least 2 years’ experience in the operation of factory machinery with motors and hydraulic systems
  • Diploma or degree in a technical field or biological science related discipline.

 Quality Control Chemistry Analyst

Deadline: 2022-01-21 

Key responsibilities:

  • Strict observation of GMP and GLP
  • Identify gaps in GMP and GLP implementation and appropriate mitigations.
  • Receipt of raw materials
  • Quarantine of raw materials and Finished products
  • Sampling of Raw materials, process water and processes.
  • Analysis of samples and interpretation of results
  • Data trending, OOT and OOS investigation.
  • Evaluate the effectiveness of laid down procedures and identify the need to review them.
  • Generation or review of Standard Operating procedures, Standard testing procedures Certificate of analysis etc.
  • Preparation of laboratory working reagents.


  • Bachelor’s Degree in Industrial Chemistry, Analytical Chemistry or Biochemistry
  • At least 3-5 years’ experience in a similar role in the Pharmaceutical Industry will be an added advantage.
  • MUST fully understand all the operations taking place in the entire quality control laboratory  (chemistry and microbiology laboratory);
  • Good knowledge of Pharmaceutical Quality Management Systems & Good Laboratory Practice;
  • Conversant with WHO –Good Manufacturing Practices;
  • Good written and oral communication skills.
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