Audio Post Production Jobs in Johannesburg
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Scientific / QA
- Last 7 days (17)
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Festive - Production Veterinarian
Astral Operations Ltd
South Africa
lesion scoring in broilers; Routine and diagnostic post-mortem evaluation of broilers and breeders; Audits science; Veterinary experience in commercial poultry production will be beneficial; Registered with the South
share this job on whatsappProduct Manager (yellow Machines)
Johannesburg
Up to R45 000 per month
Must have technical abilities and product knowledge
Must have experience working with machinery models like CATERPILLAR etc
Product Manager
Demonstrate abilities in identifying advantages of Liugong products through the comparative study of sites and competitors products and activities advantage/competitive advantages of Liugong products
Develop and propose products development and improvement the comparative study on sites and competitors products and follow up with headquarter about strategies
Veterinarian Johannesburg, Pretoria, South Africa
Astral Operations LtdSouth Africa
lesion scoring in broilers; Routine and diagnostic post-mortem evaluation of broilers and breeders; Audits science; Veterinary experience in commercial poultry production will be beneficial; Registered with the South
Associate Researcher (fixed Term Contract Wits Rhi)
Aj PersonnelHillbrow
Operating Procedure (SOP) Ensure quality assurance of audio files, transcripts, and debrief reports from qualitative self-management Follow through to ensure that quality and productivity standards of own work are consistently and accurately
Associate Researcher Hillbrow, South Africa
Aj PersonnelHillbrow
Operating Procedure (SOP) Ensure quality assurance of audio files, transcripts, and debrief reports from qualitative self-management Follow through to ensure that quality and productivity standards of own work are consistently and accurately
Associate Researcher (fixed Term Contract Wits Rhi)
Hillbrow
Procedure (SOP)
Qa Pharmacist Johannesburg
Divergent Recruit Pty LtdSouth Africa
Registration with SAPC (ESSENTIAL) Minimum of 3 - 5 years' post qualification working experience in a pharmaceutical Systems, Documentation Control, Human Recourse, Production, S5 & S6 Controls Highly experienced on SYSPRO business requires. Ensure release of 3" party products on time. Sends relevant QA reports to contract contract givers for approval. Assist with product release when required. Documentation Ensure that all queries Registration with SAPC (ESSENTIAL) Minimum of 3 - 5 years' post qualification working experience in a pharmaceutical
Qa Pharmacist (3-months Ftc) Market Related
Divergent Recruit Pty LtdSouth Africa
Registration with SAPC (ESSENTIAL) Minimum of 3 - 5 years' post qualification working experience in a pharmaceutical Systems, Documentation Control, Human Recourse, Production, S5 & S6 Controls Highly experienced on SYSPRO business requires. Ensure release of 3" party products on time. Sends relevant QA reports to contract contract givers for approval. Assist with product release when required. Documentation Ensure that all queries Registration with SAPC (ESSENTIAL) Minimum of 3 - 5 years' post qualification working experience in a pharmaceutical
Ra Pharmacist Jhb - Northern Suburbs
Ultra Personnel : Pharmaceutical, Insurance, EngineeringNorth Johannesburg
submission of variations, application for new products and life cycle maintenance in accordance with procedures and legislation for drug development, product registration, line extension and license maintenance the regulatory submission progress of specific products and ensure support needed to drive performance priorities. License maintenance: Ensure all post-approval product maintenance activities including CMC variations technical changes to the label or the packs, PBRERs, and post approval commitments are submitted and approved
Ra Pharmacist & Deputy Responsible Pharmacist
Ultra Personnel : Pharmaceutical, Insurance, EngineeringNorth Johannesburg
submission of variations, application for new products and life cycle maintenance in accordance with procedures and legislation for drug development, product registration, line extension and license maintenance the regulatory submission progress of specific products and ensure support needed to drive performance priorities. License maintenance: Ensure all post-approval product maintenance activities including CMC variations technical changes to the label or the packs, PBRERs, and post approval commitments are submitted and approved
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