Senior Pharmaceutical Quality Control Analyst

Placements24; Bloemfontein; Hybrid; ZAR 900,000 - 1,200,000; Full time

Benefits offered by this job

Health insurance

Retirement plan

Training opportunities

Paid time off

Hybrid work

Job summary

Placements24 is seeking a Senior Pharmaceutical Quality Control Analyst for a Bloemfontein-based role within a leading pharmaceutical company. The role focuses on rigorous analytical testing, method development, and regulatory-compliant documentation to ensure product quality.

The position requires 5+ years in pharmaceutical QC, expertise with analytical instrumentation, and strong GMP/GLP knowledge. Hybrid work arrangement supports in-office collaboration with remote flexibility.

Qualifications

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

Responsibilities

• Conduct analytical testing of raw materials, in‑process samples, and finished products using HPLC, GC, UV‑Vis, FTIR.
• Develop, validate, and transfer analytical methods per regulatory guidelines (ICH, GMP).
• Interpret results, troubleshoot issues, and document findings in notebooks and reports.
• Prepare Certificates of Analysis (CoA) and ensure documentation meets regulatory standards.
• Participate in investigations, CAPAs, and root cause analysis.
• Maintain and calibrate laboratory equipment to ensure quality data.

Skills

Analytical testing

Regulatory knowledge

Problem solving

Documentation

Education

Bachelor's or Master's in Pharmacy/ Chemistry

Tools

HPLC

GC

UV-Vis

FTIR

Spectroscopy

Job description

About the Role

Our client, a leading entity in the pharmaceutical sector, is actively seeking a highly skilled and experienced Senior Pharmaceutical Quality Control Analyst to join their dynamic team in **Bloemfontein**. This pivotal role demands a rigorous approach to ensuring the highest standards of quality and compliance across all manufactured pharmaceutical products. The successful candidate will be instrumental in maintaining the integrity of our client's operations and contributing to the development and release of safe and effective medicines. This position offers a unique opportunity to work within a well-established company that values innovation and employee development within the vibrant **Free State** province. You will be part of a team dedicated to excellence, playing a crucial part in the company's mission to improve global health through superior pharmaceutical products. The hybrid work model allows for a balance between focused in-office collaboration and the flexibility of remote work, ensuring productivity and well-being.

Key Responsibilities

• Conduct comprehensive analytical testing of raw materials, in-process samples, and finished pharmaceutical products using various laboratory techniques (e.g., HPLC, GC, UV-Vis, FTIR).
• Develop, validate, and transfer analytical methods in accordance with regulatory guidelines (ICH, GMP).
• Interpret test results, troubleshoot analytical issues, and document all findings accurately in laboratory notebooks and reports.
• Prepare Certificates of Analysis (CoA) and ensure all documentation meets regulatory compliance standards.
• Participate in quality investigations, root cause analysis, and implementation of corrective and preventive actions (CAPAs).
• Maintain laboratory equipment, ensuring it is calibrated, qualified, and in good working order.
• Collaborate with cross-functional teams, including R&D, Production, and Regulatory Affairs, to resolve quality issues and support product lifecycle management.
• Mentor and provide technical guidance to junior analysts, fostering a culture of continuous learning and improvement within the QC department.
• Stay updated with the latest scientific advancements and regulatory requirements in pharmaceutical quality control.

Requirements

• Bachelor's or Master's degree in Pharmacy, Chemistry, Biochemistry, or a related scientific field.
• A minimum of 5 years of progressive experience in pharmaceutical quality control or a related analytical laboratory setting.
• Proven expertise in operating and maintaining advanced analytical instrumentation (HPLC, GC, spectroscopy).
• Strong understanding of Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and relevant regulatory guidelines.
• Excellent analytical, problem-solving, and critical thinking skills.
• Proficiency in data analysis and report writing.
• Strong interpersonal and communication skills, with the ability to effectively collaborate with team members and stakeholders.
• Detail-oriented with a commitment to accuracy and quality.
• Previous experience in a **Bloemfontein**-based pharmaceutical or chemical industry is advantageous.

Benefits

• Competitive annual salary package.
• Comprehensive health insurance and retirement savings plan.
• Opportunities for professional development, training, and career advancement.
• Generous paid time off and holiday leave.
• A supportive and collaborative work environment within a leading pharmaceutical company.
• Hybrid work arrangement for improved work-life balance.
• Access to state-of-the-art laboratory facilities and cutting-edge technology.