Job Opportunities at Vixa Pharmaceutical Company Limited

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.

Note: Only Shortlisted candidate will be contacted.

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Job Description
Microbiologists undertake laboratory analysis and monitoring of microbial cultures, samples and drugs using specialized equipment/devices and a range of identification methods and clinical trials.
Job Responsibilities

• Analyzing samples collected and interpreting and recording results and data
• Carry out water analysis
• Collect samples and carry out all specified and relevant microbiological test on water, raw materials, bulk/in-process materials and finished goods
• Conduct environmental microbiological test according to cGMP specifications
• Ensure that all processes are done under cGMP compliant conditions
• Develop and execute test processes to ensure that all objectives are met.
• Implement and monitor test procedures to assess functionality, reliability, performance, and quality of the product at various stages.Identify and remedy defects within the production process that relate to microbiology.

Qualifications and Requirements

• A minimum of HND / B.Sc. in Microbiology
• Minimum of 2 years
• experience in 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.

Note: Only Shortlisted candidate will be contacted.