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Consultant for Quality Management Systems for Pharmaceutical Sector

JOB SUMMARY

Company USP Ghana
Industry Public Health
Category Medical/Pharm...
Location West Africa
Job Status Contractor/Co...
Salary Attractive
Education B.Sc./M.Sc.
Experience 10 years
Job Expires Jun 14, 2021
Contact ...
 

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

USP seeks Quality Management Systems/Quality Control expert who will provide consulting services as well as serve as a resource person for training programs organized at USP Ghana site and countries across Africa.

Scope of Work / Responsibilities

  • Delivery and preparations of materials covering content such as international guidelines and standards for therapeutics and diagnostics e.g., use of WHO global benchmarking tool (GBT) for assessment of regulatory systems, WHO GPPQCL, knowledge of accreditation programs (e.g., ISO/IEC 17025, ISO 17043, 15189, 15190, 45001, 14001, 29 CFR 1910) and Quality Management Systems (ISO 9001), knowledge of ICH guidelines, WHO GMP for Pharmaceuticals Products – Main principles.
  • Preparations and/or review of training materials and conduct training (online/virtual, in-country and/or in-person) covering content such as pharmaceutical QC equipment qualification, computerized systems validation, calibration/verification and basic preventive maintenance and laboratory quality management systems.
  • Updating of existing training materials and conduct training in QMS.
  • Delivery of trainings in pharmaceutical Quality Control Techniques.
  • Recordings of QMS and Basic laboratory equipment qualification, preventive maintenance and calibration/verification training materials for online courses.

Required Skills or Experience

  • BS/MS degree in Chemistry/Biochemistry/Pharmacy.
  • A minimum of 10 years of relevant quality assurance, analytical laboratory, compendia, and/or regulatory experience.  Experience in a pharmaceutical, biotech, or other regulated industry.  An equivalent combination of education and experience is acceptable.
  • Auditing experience is required.
  • Experience and thorough understanding of the pharmaceutical product development process and regulatory requirements, common analytical methods, and procedures.
  • Ability to generate reports and recommendations on likely future topics.
  • Excellent written and oral communication skills, including experience in training.
  • Should have sound knowledge of industrial hygiene\

How To Apply

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