Chemical Engineer - Quality Assurance

Placements24; Paarl; Sur place; ZAR 650 000 - 780 000; Plein temps

Avantages offerts par ce poste

Performance incentives

Medical benefits

Retirement plans

Certifications training

Paarl exposure

Résumé du poste

Placements24 is seeking a meticulous Chemical Engineer to lead QA in their Paarl facility. You will develop validation protocols, investigate deviations, and drive CAPAs to uphold regulatory compliance and product excellence.

The ideal candidate holds a bachelor’s degree in Chemical Engineering with 3–5 years in QA/QC within chemical or pharmaceutical manufacturing, and you bring strong QMS/ISO/GMP knowledge, plus proficiency in SPC, data analysis, and precise documentation.

Qualifications

• Bachelor’s degree in Chemical Engineering required.
• 3–5 years QA/QC experience in chemical/pharma manufacturing.
• Strong knowledge of QMS, ISO standards or GMP.
• Proficient in SPC and data analysis software.
• Excellent documentation and reporting skills.

Responsabilités

• Develop and execute validation protocols for new and existing chemical processes and equipment.
• Investigate product and process deviations, identify root causes, and implement CAPAs.
• Perform data analysis on production batches to ensure consistency and identify trends.
• Review and approve batch records and quality control documentation.
• Collaborate with production and R&D teams to resolve quality-related issues.
• Participate in internal and external audits, ensuring compliance with quality standards.

Connaissances

QA/QC experience

Data analysis

Statistical analysis

Documentation

Problem solving

Attention to detail

Formation

Bachelors in Chemical Engineering

Outils

Statistical software

Description du poste

About the Role

Our client is seeking a meticulous Chemical Engineer to join their Quality Assurance department in Paarl. This role is crucial in ensuring that all chemical products and processes meet stringent quality standards and regulatory requirements. You will be involved in process validation, deviation investigations, and continuous improvement initiatives to uphold the integrity and consistency of our client's manufacturing operations. This position requires a keen eye for detail and a strong commitment to quality and compliance.

Key Responsibilities

• Develop and execute validation protocols for new and existing chemical processes and equipment.
• Investigate product and process deviations, identify root causes, and implement corrective and preventive actions (CAPAs).
• Perform data analysis on production batches to ensure consistency and identify trends.
• Review and approve batch records and quality control documentation.
• Collaborate with production and R&D teams to resolve quality-related issues.
• Participate in internal and external audits, ensuring compliance with quality standards.

Requirements

• Bachelor's degree in Chemical Engineering.
• 3-5 years of experience in quality assurance or quality control within a chemical or pharmaceutical manufacturing environment.
• Strong understanding of Quality Management Systems (QMS), ISO standards, or GMP guidelines.
• Proficiency in statistical process control (SPC) and data analysis software.
• Excellent documentation and reporting skills.
• Detail-oriented with strong problem-solving capabilities.

Benefits

• Competitive salary and performance incentives.
• Comprehensive benefits package including medical and retirement plans.
• Opportunities for professional certifications and training in quality management.
• Exposure to diverse quality assurance challenges in the Paarl region.
• A stable and professional work environment focused on product excellence.