Research and Development Officer at Emzor Pharmaceutical Industries Limited

Job Overview

Location
Lagos, Lagos
Job Type
Full Time
Date Posted
1 year ago

Additional Details

Job ID
117371
Job Views
88

Job Description






SUMMARY OF JOB RESPONSIBILITIES:




  • Initiate stability studies for new and existing products

  • Withdraw and transfer stability samples withdrawn to relevant units’ laboratories.

  • Follow up with collation of stability result from QC, IPC and Microbiologist.

  • Characterization of innovator/reference brands.

  • Carry out processing details for new product trials.

  • Carry out laboratory trials for reformulation of existing products.

  • Follow up on quality control analysis for new product trials.



KEY RESULTS AREAS




  • Laboratory scale trial processing

  • Intermediate product reprocessing

  • Stability studies of finished product and new product

  • Process validation and analytical method validation



KEY PERFORMANCE INDICATORS




  • New product development

  • Analysis of Innovator brands

  • Carry out processing details for new product trial

  • Stability Studies

  • Initiation of stability studies of at least three batches of a product per year

  • Ensure parameters for the stability chamber is always maintained.

  • Follow up on stability results from QC, IPC and Microbiology laboratory.



JOB COMPETENCIES



Qualifications




  • Bachelor’s Degree or HND in any Science related discipline (Chemistry-Based).



Experience:




  • Minimum of three (3) years in pharmaceutical manufacturing environment or a related environment



Relevant Skills:




  • Problem-solving: Ability to identify and solve complex formulation-related problems.

  • Literature review: Familiarity with scientific literature and ability to stay up-to-date with

  • the latest developments in pharmaceutical formulation.

  • Communication: Effective communication with cross-functional teams, including R&D, manufacturing.

  • Teamwork: Ability to work collaboratively with colleagues.

  • Time Management: Effective time management to balance formulation development, testing, and documentation.



Technical Competencies




  • Understanding of Unit Process and operations

  • Pharmaceutical & Therapeutic Knowledge.

  • Understanding of the Chemistry of API and excipients.

  • Understanding of regulatory guidelines

  • Good Manufacturing Practice and Good Documentation Practice.

  • Understanding Validation, qualification and technology transfer.

  • Understanding of materials properties, and their applications in formulation.



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