Quality Systems Support Officer
Job Description:
Purpose:
A leading organisation in the pharmaceutical industry is seeking a Quality Systems Support Officer (Fixed Term Contract) who will be responsible for supporting the Quality Assurance function by clearing a backlog of SAP-related quality system tasks, including incidents, change controls, customer complaints, and document reviews, while ensuring compliance with GMP and internal quality standards
Key Job Outputs:
- Assist in completing quality risk assessments related to change notifications, particularly supplier and material changes
- Review and approve documents due for routine cycle review, including minor formatting and administrative updates
- Compile investigation reports for customer complaints and adverse drug reactions
- Assess and manage historical/open notifications within the system, including liaising with notification owners
- Complete incident and deviation notification tasks based on complexity, risk, and specific case requirements
- Ensure timely closure of all assigned notifications and document reviews within agreed timelines
- Collaborate with internal stakeholders to obtain required information for task completion
- Maintain accurate and compliant records within SAP/eQMS systems
Core Competencies:
- Strong understanding of pharmaceutical Quality Assurance processes
- Proficiency in SAP and electronic Quality Management Systems (eQMS)
- Solid knowledge of GMP (Good Manufacturing Practices)
- Strong attention to detail and documentation skills
- Analytical thinking and problem-solving ability
- Ability to manage high volumes of work and meet deadlines
- Effective communication and stakeholder engagement skills
- Ability to work independently in an onsite, collaborative environment
Qualifications:
- Degree or Diploma in a relevant scientific field (e.g. Pharmacy, Microbiology, Biotechnology or related)
Experience:
- Proven experience in pharmaceutical Quality Assurance
- Hands-on experience with SAP or similar eQMS systems
- Experience working within GMP-regulated production environments
- Exposure to handling deviations, change controls, and customer complaints
- Experience with sterile or biological products will be advantageous
Salary: Market related
Should you not hear from us within 2 weeks, kindly consider your application as unsuccessful.
All personal information received will be processed in accordance with The Protection of Personal Information Act No. 4 OF 2013