Job Vacancies at United States Pharmacopeia Convention (USP)

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The U.S. Pharmacopeial Convention (USP) is an 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.

We are recruiting to fill the positions of:

 

 

Job Title: Sample Collector for Anti-malarial PMS Study

Locations: Abuja, Akwa Ibom, Bauchi, Benue, Cross River, Ebonyi, Kebbi, Nasarawa, Plateau, Oyo, and Zamfara
Period of Performance: October 25 – 29, 2021 (One Week)

Summary of the Position

  • Sample collectors as Mystery shoppers for first round of anti-malarial PMS study across eleven (12) PMI States.

Role and Responsibilities

  • The sample collectors will act as Mystery shoppers on a covert mission to pick samples of antimalarial across three (3) senatorial districts across eleven states plus the FCT (12) PMI States (Akwa Ibom, Bauchi, Benue, Cross River, Ebonyi, Kebbi, Nasarawa, Plateau, Oyo, Sokoto, Zamfara and FCT).
  • Undergo virtual interview
  • Courier collected sample to PQM+ Abuja office
  • Manage funds for procurement, write expense reports and retire unused funds
  • Write a report on sample collection operations.
  • Undergo virtual sample collectors
  • Procure sample collection materials
  • Covertly sample antimalarial across three (3) senatorial districts
  • Document and tabulate sample on sampling form and electronic forms
  • Label collected sample appropriately

Deliverables Expected:

  • Collect the required amount of antimalarial sample
  • Courier the collected sample to PQM+ Abuja office
  • Write expense report and retire unspent fund
  • Write report on Sampling
  • Submit all electronic records, hard copy forms and reports to team lead.

Key Requirements

  • Discipline in Pharmacy or any of the Life Sciences background.
  • Preferably must be in the sampling state
  • Should be able to speak the local dialect fluently
  • Good understanding of the public and private drug outlet
  • Should be able to speak the local dialect fluently.

Preferred Qualification Required:

  • Country the work is expected to be completely done is Nigeria

Remuneration
USP offers an impressive benefits and allowances package.

 

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Job Title: Technical Officer, Chemistry, Manufacturing & Control (CMC)

Location: Lagos

Summary of the Position

  • The Technical Officer, Chemistry and Manufacturing Control (CMC) will provide technical assistance to POM+ supported manufacturers to produce quality assured maternal newborn and child health (MNCH), nutrition and malaria medical products.
  • The candidate must have expert skills in pharmaceutical manufacturing, dossier evaluations / submission and facility inspection. Assessment for compliance to Good Manufacturing Practice (GMP).
  • S/he must understand the pharmaceutical development process from pre-clinical development through life cycle management.
  • She will provide technical assistance to MRA in aspects of dossier evaluation and inspection of facilities for compliance to GMP.
  • Have good understanding of pharmaceutical regulatory environment for pharmaceutical manufacturing.
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Roles and Responsibilities

  • Provides technical assistance to local manufacturer’s in-country to implement and comply with GMPs and in the development of dossiers to submit for WHO prequalification.
  • Facilitate the development of quality management documentation in compliance with WHO guidelines.
  • Build capacity on dossier compilation, GMP compliance, GxPs for staff and identified gaps in knowledge towards compliance on WHO guidelines,
  • Conduct mock GMP inspection(s) in preparation for WHO P0, MRA/ body/Multilateral procurement agency inspections as welt as effective implementation of CAPA plans.
  • Facilitate the development ol rn4ious training programs to ensure sustainability and knowledge transfer.
  • May provide mentorship to staff as applicable
  • Actively contribute to annual programmatic and resource planning process and to the development of quarterly and annual reports.

Basic Qualifications

  • Minimum of 6+ years of experience leading and implementing technical assistance programs in expanding access to global health products and pharmaceuticals.
  • Bachelor’s Degree in Pharmacy, Pharmaceutical Science Chemistry, Engineering, or Science related field of study required.
  • Working understanding of Chemistry, Manufacturing and Controls, good manufacturing practice, dossier evaluation and inspection.
  • Direct experience implementing USAlD4unded programs.
  • Direct experience and understanding of WHOP pre-qualification process.
  • written (especially technical writing) and oral communication skills.
  • Experience working with regulatory bodies and/or local manufacturers.
  • Willingness to travel at least 25% of the time.

Preferred Qualification Required:

  • Minimum of 3+ years of people managerial experience and skills
  • Experience in at least one of the following health areas: HIV/AIDS, Malaria, TB, NTDs, AMR, MNCH
  • Country the work is expected to be completed done: Nigeria.

Restrictions or Key Requirements for The position:

  • Must be in Lagos
  • Should be able to speak the local dialect fluently.

Remuneration
USP offers an impressive benefits and allowances package.

 

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Job Title: Technical Officer, QA / QC & RSS

Location: Abuja

Summary of the Position

  • The Technical Officer, Quality Assurance / Quality Control (QA/QC) will provide technical assistance to the Agency for Food and Drug Administration and Control (NAFDAC) network of laboratories to build their capacity to ensure the quality of medical products circulating in the Nigeria market.
  • They must possess a deep understanding of the pharmaceutical regulatory environment a low Income arid middle-income countries to provide technical oversight for strengthening the capacity of laboratories responsible for assessing the quality of medical products and vaccines.

Role and Responsibilities

  • Facilitates the development of in-house training programs to ensure sustainability and transfer of knowledge within NAFDAC laboratories
  • Advises on the Interventions to address institutional development plans on the findings of the WHO Global benchmark assessment related to laboratory testing
  • Leads the rollout of risk- post-marketing surveillance and the uptake and application of the MadRS tool
  • Provide technical assistance for ISO/IEC 17025:2017 accreditation and/or WHO prequalification by assessing, auditing, preparing and reviewing laboratory processes end procedures
  • Assist in preparation of quality control laboratories for WHO inspections, including assistance in strengthening GelS procedures to prepare for WHO Inspections, conducting of mock audits and preparation of laboratory information files to be submitted to WHO.
  • Assist laboratories during WHO inspections and in the development and implementation of CAPA plans
  • Provide oversight of local partners and consultants Involved In laboratory activities
  • Keep abreast of the steel regulatory trends and WHO guidance
  • Actively contribute to annual programmatic and resource planning process and to the development of quarterly and annual reports
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Basic Qualifications

  • Bachelor’s Degree in Pharmacy, Pharmaceutical Science, Chemistry, Engineering or Science related field of study required
  • Six (6) years of relative experience leading and providing technical assistance to quality control laboratories in medicine regulatory authorities (MRA5) 10 ensure the availability of quality medical products.
  • Direct experience implementing USAID-funded programs.

Skills Sought:

  • Bachelor’s Degree in Pharmacy, Pharmaceutical Science, Chemistry, Engineering or Science related field of study required
  • Working knowledge and understanding of regulatory strengthening In Nigeria with an emphasis on Quality Assurance/Quality Control of medical products
  • Strong written (especially technical writing) end oral communication skills
  • Willingness to travel at least 25% of the time.

Preferred Qualification Required:

  • Two years of people management experience and skills
  • Direct experience with and understanding of WHO global benchmarking tool
  • Experience in at least one of the following health areas: HIV/AIDS, Malaria, TB, NTDs, AMR, MNCH
  • Country the work is expected to be completed done: Nigeria.

Restrictions or Key Requirements for the Position:

  • Must be in Abuja
  • Should be able to speak the local dialect fluently.

Remuneration
USP offers an impressive benefits and allowances package.

 

 

How to Apply
Interested and qualified should send their CV to: [email protected] using the Job as the subject of the email.

Note

  • 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 orany other protected class.
  • We are committed to working with and providing reasonable accommodation to individuals with dieabilities.
  • USP does not accept unsolicited resumes from 3rd party recruitment and is not responsible for fees from recruiters or other agencies except under specific written agreement with USP. It is PQM+ intent to grant this offer to the most suitable candidate

Application Deadline  15th November, 2021 (4:00 PM).

 

RECOMMENDED JOB SEARCH

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  3. Banking and Finance Jobs

  4. International NGOs Recruitment

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  8. Customer Service Jobs

 

 

 

Important Notes

The above statements are intended to describe the general nature and level of work to be performed by people assigned to this job.

They are not to be construed as an exhaustive list of all responsibilities, duties and skills required of personnel so classified.

All personnel may be required to perform other responsibilities in addition to those specified from time to time, as needed.

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We do not charge any application, processing, training, interviewing, testing or other fee in connection with the application or recruitment process. Should you receive a solicitation for the payment of a fee, please disregard it.

Furthermore, please note that emblems, logos, names and addresses are easily copied and reproduced. Therefore, you are advised to apply particular care when submitting personal information on the web.

We are an equal opportunity employer and value diversity inclusion. We do not discriminate on grounds of colour, race, nationality, religion, age, ethnic origin, disability, gender, marital status, or sexual orientation in our employment practices

Our people are all equally gifted in unique ways: we come from diverse traditions, personal experiences and points of view. And we want to include yours, Are you ready to inspire us with your ideas?

We encourage all applicants to apply and does not practice any discrimination in any recruitment process.

Applications submitted after the deadline will not be considered.

Due to the urgency of the position, we have the right to recruit a candidate who matches the required profile before the above deadline

Only qualified candidates will be invited for interview

Publisher’s Note:

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