Quality Control Analyst - Pharmaceutical Manufacturing

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

Benefits offered by this job

Competitive salary

Medical benefits

Retirement benefits

Paid leave

Continuous learning

Job summary

Placements24 is seeking a meticulous Quality Control Analyst for a pharmaceutical manufacturer in Mossel Bay. You will perform analytical testing on raw materials, in-process samples, and finished products to ensure compliance with quality specs and regulatory standards.

The role requires a solid foundation in analytical chemistry, hands-on experience with HPLC and GC, and a strong commitment to accurate record-keeping within GMP environments.

Qualifications

• Bachelor's degree in Chemistry or related field.
• Minimum 2 years as QC Analyst in pharma or regulated facility.
• Proficient with analytical instrumentation, GMP/GLP knowledge.

Responsibilities

• Conduct tests on raw materials, intermediates, and finished products.
• Prepare reagents and standards for testing.
• Operate and calibrate laboratory equipment and maintain logs.
• Document results and observations per GMP.
• Investigate OOS results and deviations.

Skills

Analytical chemistry knowledge

Attention to detail

Record-keeping

Team collaboration

Education

Bachelor's degree in Chemistry/Analytical Chemistry

Tools

HPLC

GC

UV-Vis

Karl Fischer titration

Job description

About the Role

Our client, a reputable pharmaceutical manufacturer located in Mossel Bay, is seeking a meticulous Quality Control Analyst to join their laboratory team. In this role, you will perform critical testing on raw materials, in-process samples, and finished products to ensure they meet stringent quality specifications and regulatory standards. Your work directly contributes to the safety and efficacy of the medications produced, upholding the company's commitment to quality. This position requires a strong foundation in analytical chemistry, excellent laboratory skills, and a dedication to maintaining accurate records in a regulated environment.

Key Responsibilities

• Perform a variety of analytical tests on raw materials, intermediates, and finished pharmaceutical products using techniques such as HPLC, GC, UV-Vis, and Karl Fischer titration.
• Prepare reagents, samples, and standards accurately for testing.
• Operate and maintain laboratory equipment, ensuring proper calibration and functioning.
• Document all testing procedures, results, and observations meticulously in compliance with GMP guidelines.
• Investigate out-of-specification (OOS) results and participate in deviation investigations.
• Adhere to all safety protocols and environmental regulations within the laboratory.

Requirements

• Bachelor's degree in Chemistry, Analytical Chemistry, or a related scientific field.
• Minimum of 2 years of experience as a QC Analyst in a pharmaceutical or regulated manufacturing environment.
• Proficiency with analytical instrumentation, particularly HPLC and GC, is essential.
• Solid understanding of GMP principles and good laboratory practices (GLP).
• Excellent attention to detail, accuracy, and record-keeping skills.
• Ability to work effectively both independently and as part of a team in a laboratory setting in Mossel Bay.

Benefits

• Competitive annual salary and potential for performance-based incentives.
• Comprehensive medical and retirement benefits.
• Paid time off and holiday leave.
• Exposure to modern analytical techniques and continuous learning opportunities.
• A stable and professional work environment focused on product quality in the Western Cape.