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Biologics Consultant

JOB SUMMARY

Company USP Ghana
Industry Public Health
Category Public Health
Location Accra
Job Status Contractor/Co...
Salary Attractive
Education B.Pharm or M....
Experience 5 years
Job Expires Dec 19, 2021
Contact Erica Asante-...
 

Company Profile

The U.S. Pharmacopeial Convention (USP) USA is an independent scientific organization that collaborates with the world's top experts in health and science to develop quality standards for medicines, dietary supplements, and food ingredients. USP brings together more than 1,100 talented professionals across five global locations to deliver its mission to strengthen the supply of safe quality medicines and supplements worldwide. USP is proud to be an equal employment opportunity employer (EEOE) and affirmative action employer. Employment selection and related decisions are made without regard to sex, race, age, disability, religion, national origin, color, veteran status, sexual orientation, gender identity, or any other protected class. We are committed to working with and providing reasonable accommodation to individuals with disabilities. USP does not accept unsolicited resumes from 3rd party recruitment agencies and is not responsible for fees from recruiters or other agencies except under a specific written agreement with USP

Job Description

Purpose
USP Ghana is involved with capacity building of personnel in the Regulatory Systems Strengthening sector and particularly in the area of Evaluation of biological dossiers. Thus, USP-Ghana needs a consultant who will be responsible for performing geared towards capacity building in Biologics evaluation.

Scope of Work
The consultant will be charged with the development and implementation of the following:

  • Development of materials required for capacity building in Evaluation of biological dossiers. Materials must include topics such as:
  • Manufacturing, GMP, validation, stability, and specifications for biologics.
  • Biologic product manufactured in prokaryotic cell and mammalian cell lines.
  • Evaluation of a monoclonal antibody (Mabs).
  • Manufacturing, GMP, validation, stability, and specifications for vaccines.
  • Delivery of training in Evaluation of Biologic dossiers.
  • Update of existing materials used for capacity-building activities.

Deliverables
The consultant will provide the following upon resumption of the above role:

  • Training materials
  • Training reports
  • Future areas for training or further capacity building

Required Skills or Experience

  • Successful consultant should have enough experience in Regulatory Systems Strengthening activities (experience working with Medicines Regulatory Authorities is an advantage) i.e. 5-10 years and of a Scientific background eg, Pharmacist, Biochemist, Chemical Analyst, etc.

How To Apply

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