Job Description

• QA/QC Officer will be responsible for supporting Quality Systems and both Operational and Quality teams.

Job Responsibilities

• Developing, Reviewing and documenting of all Quality documents like Quality Manual, Standard Operating Procedures (SOPs) and Batch Manufacturing Records (BMRs) of products.
• Operational knowledge on critical laboratory equipment like HPLC, UV, FTIR, AAS, dissolution apparatus, melting point apparatus, muffle furnace and other basic laboratory equipment.
• Analytical method development and standardization of laboratory test procedures on new and existing products.
• Calibration and verification of laboratory equipment.
• Maintain and update quality control trending data base.
• Chemical and physical analysis of raw materials, intermediate and finished products.
• Preparation and standardization of volumetric laboratory reagents.
• Ensure good laboratory practices.
• In-process Quality control of production process from dispensing operations of materials, processing and packaging of finished products according to cGMP and Company’s standard specifications.

Qualifications and Requirements

• A minimum of HND / B.Sc. in Biochemistry, Chemistry, Industrial Chemistry or other related discipline
• Proven industry experience in Quality within a pharmaceutical Manufacturing Industry.
• Excellent knowledge of cGMP.
• Excellent Communication Skills, both written and verbal.
• Strong computer skills and knowledge of QA databases and applications
• Strong analytical and problem-solving skills
• Meticulous attention to details
• Self-motivation, determination and confidence.
• Ability to work with or without supervision
• Excellent knowledge of Good Laboratory Practices.