Vacancies
EMPLOYMENT DISCLAIMER
Emzor Pharmaceutical Industries Limited wishes to inform the general public that any job offers, recruitment advertisements or employment-related communications not originating from our official website www.emzorpharma.com or verified social media channels should be disregarded.
We do not request payment at any stage of our recruitment process. Any such solicitation is fraudulent and should be reported immediately.
We will not be responsible for any losses incurred by individuals dealing with unauthorized recruiters or third-party agents.
For verification or inquiries, please contact:
Name: Oluwakemi Akinsinde
Email: recruitment@emzorpharma.com
Office Phone Number: 07002255369 Ext: 2189
Stay vigilant and protect yourself from recruitment scams.
Signed,
Management
VACANCIES
COST ANALYST
QUALIFICATION: HND or BSC or evidence of certification in view. plus, part qualification of any of the accounting professional body – ICAN OR ACCA.
JOB DESCRIPTION / RESPONSIBILITIES:
- To determine the landing cost of imported raw and packaging materials
- To ascertain unit cost of finished goods for Emzor pharmaceutical industries products.
- To evaluate and appraise project tenders and special projects for management approval.
- To evaluate and appraise public private partnership projects for management considerations.
- To promptly evaluate sales or marketing proposal for discount, promotions and other sales push and advice management.
- To prepare factory efficiency reports such as downtime, output and yield analysis, labor efficiencies and wastage reports.
- Continuous check for correctness of boom material mix and cost on oracle ERP system.
SKILLS REQUIRED
- 2-3 years on the job experience on listed areas
- Knowledge and practical use of excel
- Confidence, initiative and must be a team player
- Great attention to details.
LOCATION: Lagos
**All application must be received within one week of publication** Applicants should forward their application to hremzor@gmail.com **
FORMULATION AND DEVELOPMENT MANAGER (API)
QUALIFICATION: Minimum of B.Sc., HND or equivalent in Chemistry, Biochemistry, Biological Sciences
JOB DESCRIPTION/RESPONSIBILITIES:
- 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.
- 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.
- 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.
SKILLS REQUIRED:
- 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.
LOCATION: SAGAMU
All applications must be received before 20th of march, 2024 Applicants should forward their application to hremzor@gmail.com