Lead Quality Control Analyst - On-Site GMP Leader

Placements24; George; Presencial; ZAR 900 000 - 1 200 000; Tempo integral

Vantagens oferecidas por esta oferta de emprego

Competitive remuneration package

Medical aid plan

Provident fund

Performance-based incentives

Resumo da oferta

Placements24 is seeking a Lead Quality Control Analyst for a prominent pharmaceutical manufacturer in George, Western Cape. The role oversees the QC laboratory operations, ensuring products meet regulatory and internal quality specs before release.

A hands-on leader is required to manage analytical techniques and GMP guidelines on-site. The successful candidate will guide testing, method validation, data integrity, and CAPA processes, while collaborating with Production, Regulatory, and QA teams

Qualificações

• 7+ years of progressive experience in pharmaceutical quality control, with at least 3 years in a leadership or supervisory role.
• Hands-on experience with analytical instrumentation (HPLC, GC, FTIR, UV-Vis, Dissolution) and regulatory requirements.
• Strong knowledge of GMP/GLP and SAHPRA requirements; ability to develop/validate analytical methods.

Responsabilidades

• Lead, train, and mentor a team of QC Analysts, ensuring accurate testing and protocol adherence.
• Develop, validate, and implement analytical methods for raw materials, in-process samples, and finished products.
• Oversee routine testing with HPLC, GC, UV-Vis, titration, and dissolution testing.
• Ensure GMP/GLP compliance and participate in audits as SME for QC.

Conhecimentos

Leadership

Data integrity

Problem solving

Communication

Team management

GMP knowledge

Formação académica

Bachelor's or Master's degree in Chemistry, Pharmacy, or related field

Ferramentas

LIMS

Descrição da oferta de emprego

Placements24 is seeking a Lead Quality Control Analyst for a prominent pharmaceutical manufacturer in George, Western Cape. The role oversees the QC laboratory operations, ensuring products meet regulatory and internal quality specs before release.

A hands-on leader is required to manage analytical techniques and GMP guidelines on-site. The successful candidate will guide testing, method validation, data integrity, and CAPA processes, while collaborating with Production, Regulatory, and QA teams