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Quality Assurance / Quality Control Officer at Vixa Pharmaceutical Company Limited

Vixa Pharmaceutical Firm Restricted a effectively established Nigerian Pharmaceutical Firm, Based by Chief Ebuka Okafor an entrepreneur with huge expertise within the pharmaceutical business. Vixa Pharmaceutical Co. Ltd has come of age with an imposing report of greater than 10 years of assembly the wants in healthcare by a variety of worldwide sourced, Greatest-In-Class-Medication. Vixa Pharmaceutical Co. Ltd was integrated in 1998 with the only goal of producing and advertising and marketing Pharmaceutical merchandise.

We’re recruiting to fill the place under:

Job Title: High quality Assurance / High quality Management Officer

Location: Lagos

Job Sort: Full Time

Job Area: Science

Job Description

  • QA/QC Officer will probably be chargeable for supporting High quality Techniques and each Operational and High quality groups.

Job Obligations

  • Growing, Reviewing and documenting of all High quality paperwork like High quality Guide, Commonplace Working Procedures (SOPs) and Batch Manufacturing Information (BMRs) of merchandise.
  • Operational information on essential laboratory tools like HPLC, UV, FTIR, AAS, dissolution equipment, melting level equipment, muffle furnace and different primary laboratory tools.
  • Analytical technique growth and standardization of laboratory check procedures on new and current merchandise.
  • Calibration and verification of laboratory tools.
  • Keep and replace high quality management trending information base.
  • Chemical and bodily evaluation of uncooked supplies, intermediate and completed merchandise.
  • Preparation and standardization of volumetric laboratory reagents.
  • Guarantee good laboratory practices.
  • In-process High quality management of manufacturing course of from shelling out operations of supplies, processing and packaging of completed merchandise based on cGMP and Company’s commonplace specs.

{Qualifications} and Necessities

  • A minimal of HND / B. Sc. in Biochemistry, Chemistry, Industrial Chemistry or different associated disciplines.
  • Minimal of two years expertise
  • Confirmed business expertise in High quality inside a pharmaceutical Manufacturing Business.
  • Glorious information of cGMP.
  • Glorious Communication Expertise, each written and verbal.
  • Robust laptop expertise and information of QA databases and functions
  • Robust analytical and problem-solving expertise
  • Meticulous consideration to particulars
  • Self-motivation, dedication and confidence.
  • Skill to work with or with out supervision
  • Glorious information of Good Laboratory Practices.

Utility Closing Date

twenty third October, 2020.

Methodology of Utility

and certified candidates ought to ahead their CV and Utility Letter to: [email protected] with the place utilized for as the topic of the e-mail.

Be aware: Solely shortlisted candidate will probably be contacted.

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