Senior QA Specialist – Pharmaceutical Quality & Compliance

Placements24; Klerksdorp; Híbrido; ZAR 600.000 - 900.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Medical cover

Dental and vision coverage

Vacation and sick leave

Professional development opportunities

Retirement savings plan

Collaborative work environment

Descripción de la vacante

Placements24 is recruiting a Senior Quality Assurance Specialist for its Klerksdorp facility in the North West region. The role focuses on developing and maintaining the QMS, conducting internal audits, and managing deviations and CAPAs to ensure pharmaceutical quality and regulatory compliance.

The ideal candidate has 5+ years of QA experience in pharma/medical devices, with strong cGMP/ICH knowledge, data analysis skills, and effective documentation abilities.

Formación

• Bachelor’s degree in a life science field (Pharmacy, Chemistry, Biotechnology) is required.
• Minimum 5 years of QA experience in pharmaceutical or medical device industries.
• Strong knowledge of cGMP, ICH guidelines, and regulatory requirements.
• Experience with internal audits, deviations, and CAPA systems.
• Proficiency in data analysis and technical report writing.

Responsabilidades

• Oversee and maintain the Quality Management System (QMS) to ensure cGMP and regulatory compliance.
• Conduct internal audits of processes, documentation and facilities.
• Investigate deviations and non-conformances; implement effective CAPA actions.
• Review and approve critical quality documents (batch records, SOPs, validations).
• Participate in external audits by regulators and customers.

Conocimientos

Regulatory knowledge

Auditing

CAPA

QMS implementation

Data analysis

Technical report writing

Communication

Collaboration

Educación

Bachelor's degree in Pharmacy/ Chemistry/ Biotechnology or related life science

Herramientas

Electronic QMS software

Descripción del empleo

Placements24 is recruiting a Senior Quality Assurance Specialist for its Klerksdorp facility in the North West region. The role focuses on developing and maintaining the QMS, conducting internal audits, and managing deviations and CAPAs to ensure pharmaceutical quality and regulatory compliance.

The ideal candidate has 5+ years of QA experience in pharma/medical devices, with strong cGMP/ICH knowledge, data analysis skills, and effective documentation abilities.