Categories
Pharmaceutical

Supervisor – Production at Lorache Consulting Limited

Lorache Group – Our client, a conglomerate with a big investment in the pharmaceutical sector requires the service of a suitable candidate to fill the position below:

Job Title: Supervisor – Production

Location: Ogun
Reports to: Production Head

Description
They invest in technologies and partner with others to create meaningful solutions and ultimately better results for the people they serve.

Requirements

  • Qualification: Essential: B.Pharm, M.Pharma
  • Experience: 5-7 years,
  • Job Specific Skills: Computer Literacy, Aware with ERP system, Knowledge of regulatory guidelines, Problem Solving, Team work, People Management,
  • Languages Known: English, Nigeria local language
  • Age (desirable): Below 30-32 years

Key Duties and Responsibilities
Include but are not limited to the following activities:

  • C-GMP to be followed in production manufacturing area.
  • Equipment setting, operation & preventive maintenance. Maintain equipment cleanness.
  • Allocation of manpower at all works station.
  • Put all record and manufacturing area update & online documentation on daily basis
  • Co-relation of daily production report of equipment’s, daily output analysis and performance on monthly basis.
  • Train Operators, and contract man power
  • Optimum utilization of equipment and control various breakdown, hazardous waste at manufacturing stage.
  • Shift wise Volume Delivery in Miat manufacturing stage.
  • Update ERP entries, FG reports & monthly closure in ERP system,
  • Give BMR requisition Q.A and completed BMR review before submission.
  • Co-ordinate with other department and handling of shift works in manufacturing department.
  • Give dispensing plan warehouse department.
  • Calibration of equipment/instrument as per the define frequency
  • Maintain area cleanness and status labeling practices and all time audit readiness.
  • All statutory compliance adhered FDA, Internal, CQA, Regulatory, EHS, and Audits etc.
  • Audit exposure – National Agency for Food and Drug Administration and Control (NAFDAC) & other regulatory agencies. Adhere to the compliance related CQA, EHS and internal.
  • Exposure of IPQC instruments calibration & verification.
  • Rejection monitoring and action plan, online rejection completion.
  • Co-ordinate eng. for timely rectification of maintenance issues.
  • Change parts and spare management.
  • QMS activities- exposure of SOP writing, change control & deviation.
  • RM/PM availability check from warehouse & give dispensing plan warehouse

Deadline: 30th December, 2020.

Method of Application
Interested and qualified candidates should send their CV to: lorachevacancy@gmail.com using the “Job Title” as the subject of the email.

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