Senior Quality Control Analyst

Placements24; Rustenburg; Hybrid; ZAR 350,000 - 600,000; Full time

Benefits offered by this job

Medical aid

Provident fund

Life insurance

Professional development

Work-life balance

Job summary

Placements24 is seeking an experienced Senior Quality Control Analyst for our client in Rustenburg, North West. The successful candidate will perform analytical testing across raw materials, in-process samples, and finished products, ensuring compliance with GMP and ICH guidelines.

You will lead method validation and transfer, troubleshoot equipment, and support audits in a modern QC facility. The role requires 5+ years in pharmaceutical QC, expertise in HPLC/GC, and strong data analysis, with

Qualifications

• 5+ years hands-on experience in pharmaceutical QC laboratory.
• Proficiency in HPLC and GC.
• GMP and ICH knowledge.
• Experience with method validation and transfer.
• Strong data analysis and interpretation skills.
• Excellent organizational skills and multitasking.
• Proficiency with LIMS and related software.
• Effective written and verbal communication.
• Proactive approach to quality.

Responsibilities

• Perform routine and non-routine analytical testing of materials and finished products using HPLC, GC, UV-Vis, FTIR.
• Develop, validate, and transfer analytical methods.
• Calibrate, maintain, and troubleshoot laboratory instrumentation.
• Review and interpret analytical data per specifications.
• Document all laboratory activities per GMP and SOPs.
• Investigate OOS results and deviations; participate in root cause analysis.
• Prepare Certificates of Analysis and other quality documentation.
• Contribute to audits as QC SME.
• Train and mentor junior QC analysts.
• Ensure efficient operation of the Rustenburg QC laboratory.

Skills

HPLC

GC

UV-Vis

FTIR

LIMS

Data analysis

Communication

Problem solving

Education

Bachelor's degree in Chemistry

Master's degree in Analytical Chemistry

Tools

LIMS

Job description

About the Role

Our client, a rapidly expanding pharmaceutical company, is seeking an experienced Senior Quality Control Analyst to join their dedicated team in Rustenburg, North West . This critical role will ensure that all manufactured pharmaceutical products meet the highest standards of quality, safety, and efficacy. You will be responsible for performing a wide range of analytical tests, maintaining laboratory equipment, and contributing to the continuous improvement of quality control processes. The ideal candidate will possess meticulous attention to detail, a strong understanding of analytical chemistry, and extensive experience within a GMP-regulated environment. This is a fantastic opportunity to contribute to a vital aspect of pharmaceutical production and play a key role in safeguarding public health within the Rustenburg area. You will work in a modern facility, employing advanced analytical technologies to ensure product integrity.

Key Responsibilities

• Perform routine and non-routine analytical testing of raw materials, in-process samples, and finished products using various techniques (e.g., HPLC, GC, UV-Vis, FTIR).
• Develop, validate, and transfer analytical methods as required.
• Calibrate, maintain, and troubleshoot laboratory instrumentation to ensure optimal performance.
• Review and interpret analytical data, ensuring accuracy and compliance with specifications.
• Document all laboratory activities meticulously in accordance with GMP guidelines and company SOPs.
• Investigate out-of-specification (OOS) results and deviations, participating in root cause analysis.
• Prepare Certificates of Analysis (CoA) and other quality documentation.
• Contribute to internal and external audits as a subject matter expert for QC operations.
• Train and mentor junior QC analysts, providing guidance and support.
• Ensure the efficient operation and upkeep of the QC laboratory in Rustenburg.

Requirements

• Bachelor's or Master's degree in Chemistry, Analytical Chemistry, Biochemistry, or a related scientific discipline.
• Minimum of 5 years of hands-on experience in a pharmaceutical Quality Control laboratory.
• Proficiency in a wide array of analytical techniques, particularly HPLC and GC.
• Thorough understanding of GMP regulations and ICH guidelines.
• Experience with method validation and transfer is essential.
• Strong data analysis and interpretation skills.
• Excellent organizational skills and the ability to manage multiple tasks efficiently.
• Proficiency in laboratory information management systems (LIMS) and relevant software.
• Effective written and verbal communication skills.
• A proactive approach to problem-solving and a commitment to quality in Rustenburg.

Benefits

• Our client offers a competitive salary commensurate with experience, a comprehensive benefits package including medical aid, provident fund, and life insurance.
• Opportunities for professional development and continuous learning are provided.
• You will join a supportive and collaborative team environment focused on excellence.
• The position offers a stable career path with potential for advancement within the organization.
• We believe in work-life balance and provide ample paid time off.
• Embrace a career that directly impacts patient well-being in Rustenburg.