Emzor Pharmaceutical Industries Ltd is a wholly private indigenous pharmaceutical manufacturing group founded in 1984 by Dr. Stella C. Okoli, OON. The company is into the manufacture of high quality pharmaceutical products and medical consumables.
Today, Emzor has become a household name in Nigeria and a leader in the pharmaceutical market that is known for quality products at prices that offer real value.
Applications are invited from interested and qualified candidates to apply for the latest job at Emzor Pharmaceutical Industries Ltd.
Formulation and Development Manager
Job Specifications:
- Full Time
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- Required Qualifications: BA/BSC/HND
- Location: Ogun | Nigeria.
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Job Description:
- Develop robust formulations and processes for various dosage forms as required by the company.
- Plan and contribute to project-related technical activities.
- Review and approve technical documents including Product Development Report, and other relevant documents for regulatory filing purpose.
- Interaction with procurement team, API and excipients manufacturers, Machine manufacturers, CROs and CMOs as needed.
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- Work proactively with other cross-functional groups to execute product/ process improvement and optimization, Product Lifecycle management, change controls associated with Manufacturing and Packaging master records, SOPs and protocols.
- Create and review SOPs, as well as review appropriate system documentation and test results for accuracy and completeness and compliance with SOPs/GMP requirement.
- Provide relevant documents to Regulatory Affairs in a timely manner for registration filings and Supplements filing.
- Review of batch records, process characterization reports, Annual Product Quality Review Report, validation reports and investigation reports where necessary.
- Participate in designing and approval of tablet punches and blister change parts.
- Review Formulation Development Protocol, Processes and Report to ensure the Development of robust formulations and processes.
- Plan and contribute to project-related technical activities by reviewing the activities where required.
- Review of technical document and communications shared by procurement team, API and excipients manufacturers, Machine manufacturers, CROs and CMOs as needed.
- Review of SOPs, appropriate system documentation and test results for accuracy and completeness and compliance with SOPs/GMP requirement.
- Preparation and review of Product Dossier.
- Review of batch records, process characterization reports, Annual Product Quality Review Report, validation reports and investigation reports where necessary.
- Ensure Pharmaceutical Development Protocol preparation, execution and reporting.
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- Ensure document preparation i.e., SOPs, Protocols, Master Formula Records.
- Review and/ or Approval of prepared document.
- Review and/ or Approval of technical drawing (tools and change part), where needed.
- Any additional task assigned by Management.
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Qualifications and Requirements:
- Minimum of 5-8years of relevant experience in Pharmaceutical Development
- Knowledge of Quality by Design (QbD) principles towards dosage form development, planning of trials by DOE for development and execution of trial batches.
- Knowledge of current Good Manufacturing Practices.
- Member of relevant professional body.
QUALIFICATION:
Minimum of B.Sc., HND or equivalent in Chemistry, Biochemistry, Biological Sciences.
Method of Application
Interested candidate should send their CVs to hremzor@gmail.com with the Job title as subject of the mail.
