In-Process Quality Assurance Officer

Company Details

Fidson Healthcare Plc, gladly Nigerian, is a main pharmaceutical firm which has developed from being a merchant for multinationals in 1995 to full-fledged manufacturing, sales and promoting company with a solid brand. At Fidson, we bolster each other to enormity. We motivate our kin to accomplish, yet we celebrate their accomplishments with them. Together, we work and play hard. We are employing to fill the job post underneath:

Employment Title: In-Process Quality Assurance Officer

Area: Factory-Ota, Ogun State

Office: Quality and Regulatory Affairs

Does The Cap Fit?

  • We look for proactive and imaginative people who can think and react quickly and convey great outcomes reliably. Our optimal applicants are sorted out, careful, self-propelled, open to learning, group energetic and can continue the energy to have a compelling effect in a fast-paced workplace.

Key Deliverables:

  • Undertakes general quality confirmation audit of production processes (counting however not constrained to materials apportioning, item fabricating, bundling, discharge and capacity), workforce gowning and wellbeing, generation premises and great housekeeping, products and equipment in consistence with cGMP and Fidson Quality Policy to guarantee the creation of a reliably top-notch product.
  • Guarantees that every watched incident of on-line process infringement, deviations and products quality objections are accounted for, adjusted and recorded.
  • Create routine QA consistency move reports and convey all resistant perceptions and the remedial moves made in the reports.
  • Issues line freedom for assembling and bundling forms, having found out that all vital GMP necessities have been met.
  • Guarantee great housekeeping, staff cleanliness, suitable gowning and natural neatness are kept up on all creation lines.
  • Attempt the last spot-check of completed items to find out that the last item quality is palatable before discharge and capacity.
  • Guarantees that major and basic non-similarities are expeditiously answered to the QA Manager for goals and manner.
  • Stay up with the latest/ongoing records of in-process perceptions of production procedures and product parameters.
  • Guarantees that solitary properly aligned and determined gear are utilized for assembling and other related exercises.
  • Implements severe consistency with cGMP to guarantee the make and supply of the good quality product.
  • Execute withdrawal and maintenance of delegate tests of pressed products, from production lines.
  • Guarantees all procedure control structures are precisely completed by production operators, real-time.
  • Whatever other jobs that might be appointed.

Scholarly Qualification

  • First Degree in Chemistry (Bio/Pure/Applied/Industrial), Microbiology and other related science courses.
  • Required Years of Experience: 2-4 Years
Application Closing Date

Not Specified.

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