Aseptic Technician Head of Division: Business Development

  • Full Time
  • KwaZulu-Natal
  • Applications have closed

Website National Bioproducts Institute

NBI is a private, non-profit, pharmaceutical manufacturer of human plasma-derived medicinal products. NBI's core business is to manufacture pharmaceutical products from human plasma, using a process of cold ethanol fractionation. NBI strives to meet the needs of patients and improve their quality of… read more life by providing protein therapies and services within the South and Sub-Saharan African region and diagnostic products globally.

Job Advert Summary    

Guided by its purpose to provide products for patients to alleviate pain and suffering and improve their quality of life, NBI’s vision is to be the leading African manufacturer and supplier of quality therapeutic proteins and diagnostic products.
National Bioproducts Institute NPC has a vacancy for the role of Aseptic Technician. The successful incumbent will be required to:
To assist with the production of sterilised products into bottles, vials and ampoules according to specifications and GMP compliance.
To process final product till inspection as per Standard Operating Procedures and Good Manufacturing Practices.
Applications are invited from suitably qualified and experienced candidates.

Specific SHE Requirements

Pre-employment, routine and exit medicals are compulsory due to the nature of the business
Attendance to SHE related training is mandatory
Adherence to SHE Instructions
Compliance to SHE Site Rules is compulsory
NBI uses hazardous and biologically active chemicals.
The successful candidate will be required to use proper PPE and will go through medical examinations as per OSH Act requirements

Specific Operational Requirements

The successful candidate will be required to work an 8 hour shift as rostered between 06:00-18:00 or 18:00-06:00, Monday to Sunday.
Candidate must have access to reliable transport.
May be required to work overtime to meet the business needs.
Must be prepared to work shifts/weekends/public holidays when needed.

Minimum Requirements    

Grade 12 with minimum D marks in English and minimum D marks in math, science, biology or EMS
1-2 years experience in a pharmaceutical, chemical, biotechnology or food manufacturing environment employing GMP guidelines. 

Duties & Responsibilities    
Production of final filled products

Preparation of equipment, machines and components by cleaning and sterilising as required
Assembly and disassembly of machines, equipment and product transfer sets to ensure product integrity
Operation and monitoring of all required machines and equipment
Capping and coding of filled units
Loading and offloading of the depyrogenation oven, autoclave, freezedryer and pasteuriser as per SOP
Cleaning of work machinery and work areas as per SOP
Work in the clean room and follows aseptic techniques

Sampling and environmental monitoring

Take required samples for QC, QA and microbiology testing as required.
Perform environmental and personnel monitoring as per SOPs
Ensure correct labelling of samples and product samples and transfer to respective departments

Completion of batch records and auxiliary documentation

Completes batch records timeously as required by protocols and SOPs.
Completes log books and registers for traceability and process status records

Maintain Equipment

Monitor equipment performance
Works with team members to conduct first-line maintenance of equipment
Reports incidents and machine related problems to the section head
Assist with the calibration and validation of equipment and processes by preparing components and equipment as required.

Comply with Good Manufacturing Procedures

Works with team members to execute SOPs and protocols to prepare, fill, freeze dry, cap and code ampoules, vials and bottles.
Follow the gowning procedure as per SOPs and GMP requirements
Use appropriate packaging and ensures required conditions for the appropriate storage of in-process materials and product
Dispose of waste products according to SOP’s
Follows the behavioural requirements for working in clean rooms
Participates in audits of manufacturing areas
Works with team members to assess processes and recommend methods for improving quality and efficiency
Ensure manufacturing area is clean and tidy
Attend training courses as required

Comply with the OHS act

Work in a safe manner under the indirect supervision of team members.
Wear appropriate PPE
Act as Safety Rep, Evacuation Team Leader or First-Aider as required
Reports any identified risks, hazards and incidents

Core Competencies

Leading and Influencing Others
Business Impact
Managing Relationships
Personal Leadership
Attention to detail
Oral and written communication
Ability to work individually and in a team
Understanding of sterile manufacturing
Quality awareness
Planning and Organising
Sterile Gowning
Clean Room Behaviour
Automated Filling

Deadline:11th March,2026

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