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  • Posted: Jun 23, 2020
    Deadline: Jul 3, 2020
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    Microbiologist

    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.

    go to method of application ยป

    Quality Assurance / Quality Control Officer

    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.

    Method of Application

    Interested and qualified candidates should forward their CV and Application Letter to: pharmarecruitment2online@gmail.com with the position applied for as the Subject of the email.

    Note: Only Shortlisted candidate will be contacted.

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