Quality-Forward Chemical Engineer: Validation & QA

Placements24; Stellenbosch; On-site; ZAR 600,000 - 900,000; Full time

Benefits offered by this job

Competitive salary

Medical benefits

Retirement plan

Certifications and training

Paarl region exposure

Stable work environment

Job summary

Placements24 in Paarl is seeking a meticulous Chemical Engineer to join the Quality Assurance team. You will validate processes, investigate deviations, and lead CAPA activities to ensure GMP-compliant manufacturing. The role emphasizes data-driven decisions and rigorous documentation.

Collaborating with production and R&D, you will review batch records, perform SPC-based analysis, and drive continuous improvement initiatives. A strong eye for detail and knowledge of QMS/ISO/GMP are essential.

Qualifications

• Bachelor's degree in Chemical Engineering is required.
• 3-5 years of QA/QC experience in chemical or pharmaceutical manufacturing.
• Strong understanding of QMS, ISO standards, or GMP guidelines.
• Proficiency in SPC and data analysis software.
• Excellent documentation and reporting skills; detail-oriented and strong problem-solving abilities.

Responsibilities

• Develop and execute validation protocols for chemical processes and equipment.
• Investigate deviations, identify root causes, and implement CAPAs.
• Perform data analysis on production batches to identify trends.
• Review and approve batch records and quality control documents.
• Collaborate with production and R&D to resolve quality issues.
• Participate in internal and external audits to ensure quality standards.

Skills

Quality Assurance

Documentation

Problem solving

Attention to detail

Collaboration

Education

Bachelor's degree in Chemical Engineering

Tools

SPC software

Data analysis software

Job description

Placements24 in Paarl is seeking a meticulous Chemical Engineer to join the Quality Assurance team. You will validate processes, investigate deviations, and lead CAPA activities to ensure GMP-compliant manufacturing. The role emphasizes data-driven decisions and rigorous documentation.

Collaborating with production and R&D, you will review batch records, perform SPC-based analysis, and drive continuous improvement initiatives. A strong eye for detail and knowledge of QMS/ISO/GMP are essential.