looking for a General Manager who will proactively lead the Gqeberha manufacturing plant. Tertiary qualification senior management experience in a similiar environment At least 5 years experience in a manufacturing environment knowledge of corporate governance and general management best practices In depth knowlege of development marketing management, relationship management, sales development Experience in financial management Experience measures and management Experience and knowledge in health and safety standards Experience in managing a maintenance
An established pharmaceutical manufacturing company has an opportunity for two Validation Analysts to position will report to the QC (Quality Control) Manager. NOTE - For now, the positions are on an 18-month testing. And perhaps to stand in as Acting QC Manager from September too. Job functions: Lead validation activities for a GMP pharmaceutical and API manufacturing facility. Develop protocols for executing subject matter expertise in the assessment of manufacturing deviations and investigations, change control
experienced Project Manager to manage organization of key client projects. What does a Project Manager do? As As our project manager, your job will be to coordinate people and processes to ensure that our projects involving a project's organization and timeline. Project Manager Duties Specific project manager responsibilities detailed project plans, ensuring resource availability and allocation and delivering every project on time time within budget and scope. Project Manager Requirements Project managers should have a background in
Project Document Controller, De Aar, Northern Cape. Company Name: Talent TAC Our client is committed Join us in our mission to make a difference. As a Project Document Controller, you will play a pivotal role activities and providing administrative support to our Project team. Your Responsibilities: will include but are to: Document Control: Setting up and maintaining Project Communication and Document Control Systems. Monitoring tracked. Managing SharePoint/Teams Folder Structure and adherence to requirements. Providing management tools
group requires an Senior Operations Productivity Manager based in Port Elizabeth. Mail your CV to equipmweb Vehicle progress management Review daily, vehicle trips in line with schedules Manage servicing and and and licencing requirements Manage Controllers and Drivers time efficiently At least 10 years experience
the Automotive industry, with engineering, manufacturing and support facilities located globally to service jigs, fixtures, and tooling for automotive manufacturing processes. Create detailed CAD models and engineering ensure seamless integration of tooling into manufacturing processes. Liaise with suppliers and vendors and production feedback. Generate reports on project progress, design modifications, and performance Stay updated with the latest advancements in manufacturing technology, materials, and industry trends.
within the FMCG Manufacturing sector is seeking a dynamic and well experienced Senior Project Engineer to team. The Senior Project Engineer will plan the technical side of investment projects ensuring a design design for manufacturing excellence (free of waste) and lead the execution (from investment project charter Ensures that the objectives of the investment project charter, design specifications and company standards adhered to Before starting the project design phase: Define the project scope, success criteria, and milestone
materials, does it's own R&D and testing, manufactures the products, markets and dispenses the products
An established pharmaceutical manufacturing company has an opportunity for two Validation Analysts to position will report to the QC (Quality Control) Manager. NOTE - For now, the positions are on an 18-month testing. And perhaps to stand in as Acting QC Manager from September too. Job functions: Lead validation activities for a GMP pharmaceutical and API manufacturing facility. Develop protocols for executing subject matter expertise in the assessment of manufacturing deviations and investigations, change control
An established manufacturing company is upgrading their facility to be GMP compliant for SAHPRA audits would like to implement ISO standards too. Manufacturers of pharma, cosmetics, and medical device products GMP compliance across the small/medium size manufacturing facility, to ensure the company will pass a