Location: Port Elizabeth
Job Type Classification: Permanent
Closing Date: 25 March 2024.
Salary: market related
Job Description
Overview
- Work areas and equipment should be ready, cleaned, and inspected.
- Work with and arrange raw resources.
- Examine the equipment and work area(s) for contamination.
- Clean pipes and drains to prevent pollution.
- associated administrative duties
Responsibilities
Support for Operations
Follow established procedures, regulations, and guidelines for carrying out production tasks, as well as set safety and quality standards.
Optimize your own workflow.
Determine any gaps in the policies and practices in place.
Encourage process implementation in your own field of expertise.
Exams and confirmations Examine the producing area(s) and equipment visually.
Conduct pre-production inspections in accordance with BMR, SOP, and product specifications, including environmental, scale, and equipment inspections.
Check the scale and performance of the measuring apparatus.
Material Management Measure, move, dispense, and gather raw materials for processing.
Make sure that raw materials are prepared for processing according to the specifications.
Getting Ready for Production Prepare the space and the IBCs for the manufacturing tasks.
As per SOP, prepare solutions for production-related tasks.
Routine Support Tasks
- As per the SOP and cleaning checklist, clean the work area(s) and equipment both before and after processing the materials.
- Conduct routine inspections of the equipment and equipment transfers.
- Gather manufacturing area and equipment samples for testing.
- Purge the area of contaminants by cleaning the pipes and drains.
- Help sort defective products, dispose of them, and reduce waste
- Provide details to help with campaign planning.
- Determine and document operational issues that deviate from the specification.
Reporting & Record Keeping
- Whole batch labels for records
- Full sheets of Overall Equipment Effectiveness (OEE)
- Conduct inspections of the production area(s) every 30 minutes.
- Participate in shift meetings Give information so that reports can be completed.
- Finish and compile the required paperwork.
- As needed, keep up with and update systems and records.
Job Requirements
History and expertise Matric Equivalent Certificates (NQF Level 4) or Grade 12 with 0–2 years of relevant experience
Experience in manufacturing particular work-related skills a basic understanding of the systems, equipment, processes, and procedures used in pharmaceutical manufacture. rudimentary knowledge of pharmaceutical norms and regulations
Proficiencies completing the outputs Observing protocols Acting and acquiring data
How to Apply?
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