Job Summary

We are currently recruiting for this position

  • Minimum Qualification: OND
  • Experience Level: Mid level
  • Experience Length: 5 years

Job Description


Essential Job Requirements

  • OND/B.Sc in Pharm tech, chemistry or related field

  • Minimum of 5 years working experience

  • Good communication skills

  • Meticulous attention to details

  • Critical thinker and problem-solving skills

  • Integrity and diligence to work

  • Computer literate

  • Ethical and highly coordinated

  • Experience in cGMP manufacturing

  • Excellent written and oral communication skills and ability to maintain good housekeeping

  • Flexibility of working hours based on business needs, may include some nights and occasional weekends

  • Detail-oriented with the ability to troubleshoot and resolve problems

  • Working knowledge, and progressive understanding of pharmaceutical raw material and production processes

  • Ability to communicate in a proactive and solution-focused manner, including keeping direct supervisor aware of potential issues


Job Description

  • Supervise workers during production activities to ensure compliance of laid down structures and guidelines for expected output

  • Interface with established authority, maintenance team, QA and warehouse personnel

  • Investigate causes of process failures and develop new procedures for problem-solving to produce a high-quality product and maximize output.

  • Worked independently performing troubleshooting, staff mentoring, and object-oriented research and analysis.

  • Ensure full-time compliance to cGMP and safety procedures before, during and after production

  • Developing relevant SOP’s and methods for production processes and checks

  • Maintain standard operation procedures to ensure compliance with cGMP.

  • Perform routine duties on bulk & in-process materials and finished goods.

  • Filling and recording checklists and logs pertaining to production

  • Contribute to the efficient production, transfer and release of products from start to finish.

  • Participate in cross-training with the warehouse, maintenance and QA departments.

  • Conduct investigations on questionable/problematic batches and document findings.

  • Follow detailed manufacturing instructions and SOPs to complete assigned production activities according to quality standards

  • Document and maintain records and notebooks in a neat, thorough, and accurate manner

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