Key Responsibilities

• Approving or rejecting raw and packaging materials upon delivery.
• Ensure all necessary Quality Control testing are carried out.
• Ensure all requisite validations are carried out.
• Devise and establish company’s Quality procedures, standards and specifications.
• Sampling of raw materials, packaging materials, bulk products and effluents.
• Stability studies of finished Goods.
• Ensure re-testing procedure is followed and customer complaints as well.
• Monitoring of IPQC.
• Reviewing, compiling and filling of test reports.
• Training on cGMP and monitoring of compliance with the requirement of cGMP.
• Investigating, and taking of samples in order to monitor factors, which may affect product Quality.
• Document and evaluate Batch Manufacturing records (BMRs)/Batch Packaging Records (BPRs).
• Approve specifications, sampling instructions, test methods, and other Quality Control procedures.
• Ensure internal and external calibrations are carried out and records updated.
• Storage and withdrawal of retention samples.
• Evaluation of Out of specification.
• Draft and generate in-house Certificates of analysis.
• Quality checks and documentation of checklists during receipt of incoming goods from the suppliers.
• Review and implement Quality Control SOPs.
• Ensure raw materials and packaging materials have the right status labels.
• Ensure Good laboratory practices and Good Documentations Practices are implemented.
• Perform retests or re-examine approved components, drug product containers and closures after long storage or exposure to adverse conditions.
• Online checklist.
• Product non-conformity control.
• Carry out Design and development of new products

Skills and qualifications;

• At least 2 years’ experience in a chemical manufacturing environment.
• Working knowledge of Good Manufacturing Practices (GMP),
• ISO 9001:2015, SAGE System and KAIZEN is an added advantage.
• Diploma or Degree in Analytical Chemistry or any related Field.

The deadline to apply is January 14th, 2025.