Posted on Fri 13th May, 2022 - hotnigerianjobs.com --- (0 comments)
The U.S. Pharmacopeial Convention (USP) is a scientific nonprofit organization that sets standards for the identity, strength, quality, and purity of medicines, food ingredients, and dietary supplements manufactured, distributed, and consumed worldwide. USP's drug standards are enforceable in the United States by the Food and Drug Administration, and these standards are used in more than 140 countries.
The Technical Advisor is a subject matter expert in vaccines and is responsible for the implementation of PQM+ technical assistance activities for COVID-19 vaccine manufacturing and regulation.
S/He will report to the in-country Chief of Party or his/her designee and will work under technical guidance and oversight from the HQ-based Vaccines Director.
The Technical Advisor will provide support to local manufacturers of vaccines in Africa in technology transfer and will help build national regulatory capacity for vaccines as well as the workforce competency for biologics and vaccines quality assurance.
The successful candidate will provide technical assistance on fill/finish and packaging processes for COVID-19 vaccines.
S/He will serve as a subject matter expert using knowledge to ensure cGMP compliance, fulfillment of technical requirements and regulatory guidelines as they relate to fill/finish and packaging equipment, materials, facilities, and process development.
In fulfillment of the role, the incumbent will collaborate with other USP and PQM+ staff, USP’s Global Biologics Division, local manufacturers, and vaccine regulators.
The duration of the role is contingent upon funding duration of donor (i.e. Fixed Term).
Roles and Responsibilities
Lead and coordinate the technical development and implementation of in-country COVID-19 vaccine manufacturing and regulatory work plan activities
Provide technical assistance to COVID-19 mRNA vaccines manufacturers on development, commissioning, qualification and validation of vaccine fill/finish and packaging processes.
Partner with USP and PQM+ technical team members, consultants, other PQM+ countries, vendors, and local stakeholders to assure adequate manufacturing facility design and startup.
Provide support to strengthen the National Medicines Regulatory Authority (NMRA) legal framework for vaccines manufacturing, supply, storage, distribution, and handling
Support NMRA and national control labs in the development of lot release testing capacity and in the implementation of vaccine post-marketing surveillance. Also support the GMP inspectorate of the NMRA to strengthen its capacity for regulatory oversight of vaccine manufacturers.
Liaise with HQ Vaccines Director to develop appropriate training materials and to organize the delivery of training programs targeted to local vaccine manufacturers, regulators, and quality laboratory staff.
Support manufacturers in addressing deviations and non-compliances, in conducting audits to assess compliance and the establishment of cGMPs; also, in filing of vaccine dossiers for market authorization according to NMRA’s requirements.
Coordinate efforts aimed at the identification of needs for manufacturing and laboratory equipment, materials, and processes in support to successful local production and quality assurance of COVID-19 vaccines.
Support manufacturers to identify chemistry, manufacturing, and controls (CMC) risks and continuous improvement opportunities
Gather programmatic data and develop progress reports as guided by the PQM+ HQ Vaccines Director. Also, support the development of technical and communication materials related to local manufacturing and quality of vaccines.
Bachelor of Science Degree in Pharmacy, Pharmaceutical Science, Chemistry, Biochemistry, Engineering or Science related field of study
Ten (10) years of experience in vaccines and biologics manufacturing or regulation.
Master of Science or PhD in Pharmacy, Pharmaceutical Science, Chemistry, Biochemistry, Engineering or Science related field of study
Understanding of GMP manufacturing of biologics, including vaccines
Understanding of compatibility and stability studies
Understanding of cold chain monitoring
Understanding of fill/finish and packaging processes for mRNA vaccines
Direct experience with and understanding of WHO vaccine pre-qualification and/or other regulatory authority registration processes.
Subject matter expert in vaccine/biopharmaceutical fill/finish and packaging processes
Thorough understanding of Chemistry, Manufacturing and Controls and Good Manufacturing Practices for vaccines and medicines e.g., fill and finish
Knowledge of regulatory requirements related to the development and manufacture of biologics
Strong technical writing and oral communication skills
Willingness to travel up to 25% of the time.
USP provides you with the benefits you need to protect yourself and your family today and tomorrow.
From company-paid time off, comprehensive healthcare options to retirement savings, you can have peace of mind that your personal and financial wellbeing are protected.
COVID-19 Vaccination Policy (will apply to the selected candidate(s) hired:
As a condition of employment with the United States Pharmacopeial Convention's (USP) duty to provide and maintain a workplace free of known hazards, all employees and contingent staff hired after July 1st, 2021, must be fully present vaccinated unless a reasonable accommodation is approved.