Quality Control Analyst - Pharmaceutical Raw Materials

Placements24; Vereeniging; On-site; ZAR 420,000 - 540,000; Full time

Benefits offered by this job

Competitive salary

Medical aid & retirement fund

Professional development

Job summary

Placements24 in Vereeniging, Gauteng, is seeking a meticulous Quality Control Analyst to ensure quality of incoming raw materials for pharmaceutical production. You will perform analytical tests, interpret results, maintain lab systems, and uphold GMP standards.

The role requires hands-on lab work with HPLC/GC/FTIR/UV-Vis, LIMS experience, and strong documentation and teamwork skills. Three years in QC is preferred; commuting to Vereeniging is expected.

Qualifications

• Bachelor's degree in Chemistry, Biochemistry, Pharmacy, or related.
• 3+ years in QC in pharmaceutical industry, raw material focus.
• Experience with wet chemistry and instrumental analysis (HPLC/GC/UV-Vis essential).
• Familiarity with pharmacopoeias (USP/BP/EP) and GMP guidelines.
• Independent and team player with strong communication and safety focus.

Responsibilities

• Perform analytical testing on incoming materials using various techniques.
• Ensure testing per approved specs, SOPs, and methods.
• Operate and maintain HPLC, GC, FTIR, UV-Vis, and dissolution equipment.
• Document results in notebooks and LIMS accurately and promptly.
• Investigate OOS, identify root causes, participate in CAPA actions.
• Prepare reagents and reference standards; support method validation and transfer.

Skills

Analytical testing

GMP compliance

Documentation

Teamwork

Education

Bachelor's degree in Chemistry/Biochemistry/Pharmacy

Tools

HPLC

GC

FTIR

UV-Vis

LIMS

Job description

About the Role

Our client, a leading pharmaceutical manufacturer, is seeking a meticulous and detail-oriented Quality Control Analyst to join their team in Vereeniging, Gauteng . This role is essential for ensuring the quality and integrity of all incoming raw materials used in the production of pharmaceutical products. You will be responsible for conducting a wide range of analytical tests, interpreting results, and ensuring compliance with strict quality standards and regulatory requirements. This is an excellent opportunity to contribute to patient safety and product excellence within a reputable organization known for its commitment to high standards. The role requires hands-on laboratory work and a thorough understanding of analytical techniques.

Key Responsibilities

• Perform analytical testing on incoming raw materials, excipients, and packaging components using various laboratory techniques.
• Ensure all testing is conducted according to approved specifications, methods, and Standard Operating Procedures (SOPs).
• Operate and maintain laboratory equipment, including HPLC, GC, FTIR, UV-Vis spectrophotometers, and dissolution apparatus.
• Document all test results accurately and promptly in laboratory notebooks and LIMS (Laboratory Information Management System).
• Investigate out-of-specification (OOS) results, identify root causes, and participate in corrective action investigations.
• Prepare and standardize reagents and reference standards as required.
• Participate in method validation and transfer activities as needed.
• Maintain a clean, safe, and organized laboratory environment.
• Adhere to all GMP and safety regulations at all times.

Requirements

• Bachelor's degree in Chemistry, Biochemistry, Pharmacy, or a related scientific discipline.
• Minimum of 3 years of experience as a QC Analyst in the pharmaceutical industry, with a focus on raw material testing.
• Proficiency in performing wet chemistry and instrumental analysis (HPLC, GC, UV-Vis are essential).
• Familiarity with pharmacopoeias (e.g., USP, BP, EP) and GMP guidelines.
• Experience with LIMS is a plus.
• Strong analytical skills with meticulous attention to detail and accuracy.
• Good understanding of laboratory safety practices.
• Effective written and verbal communication skills.
• Ability to work independently and as part of a team, manage time effectively, and meet deadlines.
• Must be legally authorized to work in South Africa and reside in or be able to commute to Vereeniging .

Benefits

• Competitive annual salary.
• Comprehensive medical aid and retirement fund benefits.
• Opportunities for professional development and training.
• A safe and structured work environment.
• Paid annual leave and public holidays.
• Stable employment with a reputable company.