USP Ghana Healthcare Jobs in Accra
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Job Description
Help us improve public health in Africa.
Falsified and substandard medicines threaten recent improvements to global public health--particularly in Africa. USP and its collaborators work across the region to ensure quality medicines availability. Join us in helping our partners develop skills needed to deliver quality assured medicines to citizens who need them most.
USP Ghana provides courses featuring lectures from working professionals in key sectors. We are currently recruiting experts to teach Biologics Evaluation Course.
Successful applicant should demostrate ability to teach below topics of interest and examine training candidates.
- Dossier Evaluation Introduction
- Introduction to the New Registration Guideline in CTD format
- Active Pharmaceutical Ingredients (API): General Information
- Stability of API
- Pharmaceutical Product Development
- Manufacturing: Finished Pharmaceutical Product (FPP)
- Finished Pharmaceutical Product Specification
- Process Validation and Annual Report
- Analytical Method and Validation
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1. Patiently scroll down and read the job description below.
2. Scroll down and find how to apply or mode of application for this job after the job description.
3. Carefully follow the instructions on how to apply.
4. Always apply for a job by attaching CV with a Cover Letter / Application Letter.
Job Description
Help us improve public health in Africa.
Falsified and substandard medicines threaten recent improvements to global public health--particularly in Africa. USP and its collaborators work across the region to ensure quality medicines availability. Join us in helping our partners develop skills needed to deliver quality assured medicines to citizens who need them most.
USP Ghana provides courses featuring lectures from working professionals in key sectors. We are currently recruiting experts to teach Biologics Evaluation Course.
Successful applicant should demostrate ability to teach below topics of interest and examine training candidates.
- Dossier Evaluation Introduction
- Introduction to the New Registration Guideline in CTD format
- Active Pharmaceutical Ingredients (API): General Information
- Stability of API
- Pharmaceutical Product Development
- Manufacturing: Finished Pharmaceutical Product (FPP)
- Finished Pharmaceutical Product Specification
- Process Validation and Annual Report
- Analytical Method and Validation
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